The technology of skin care is broad and differs from many other cosmetic categories because of the functional nature of many of the products. There are products that primarily have cosmetic effects and products that have very significant pharmacological effects. All products, however, are designed to interact and treat the largest organ of the body-the skin. To understand the need for the category, one must understand the business. The skin-care business is very large worldwide, with total sales of over 10 billion dollars divided between mass and prestige distribution. Mass is roughly 60 and prestige roughly 405. The largest market are Japan, at 3.5 billion dollars, the US at 2.5 billion dollars, and we stern Europe at 3 billion dollars.
Further divisions within the business are products based in sub-categories within the skin-care market. As an example, the US market is 23% hand and body moisturizers, 34% facial moisturizers. 13 % suncare and 24% cleansers (excluding bar soaps). These ratios vary between mass and prestige, and from market to market, depending on national distribution patterns, usage habits and the number of products used by consumers on a regular basis. With the exception of hand lotions, sunscreens and lip protection products, and excluding bar soaps, the market usage and purchase is dominated by women, who account for over 80% of the usage and perhaps 90% of purchase.
Anatomy and Physiology of the Skin
The skin is the largest organ of the body. It is an organ that has diverse functions, including barrier function, protection from radiation, control of body temperature and transmission of stimuli from its abundant network of nerves.
An excellent reference text on the skin is provided by Montagna and Parakkal. This text concentrates on the science of skin, which must be understood as a foundation before products affecting the skin can be appreciated or formulated. Our knowledge of the skin and its function expands every year, therefore it is imperative that one continues to study current literature, in order to remain informed. An excellent examples of the progress of the science is the evolution of the knowledge that the outermost layer of skin, the stratum corneum is 'alive'. It had previously been accepted that the stratum corneum was a collection of dead cells, with no ongoing activity beyond barrier function. It is now known that many functions do take place and may originate in this layer.
In cosmetic chemistry and the business of skin care, we are primarily concerned with the outermost layers of skin (epidermis) and, in particularly those areas that are visible, such as face, hands and legs. To understand the overall anatomy and physiology of the skin, the cross-section shown in Figure 1 should be referred to throughout the following sections.
We are all familiar with our own skin. Closer examination reveals that it is varied in appearance, structure and function in different areas of the body. The skin is generally hairy, except for the palms and soles of the feet. Hair follicles vary in density and functions, for example large terminal hair follicle, on men's scalps and beards, to small vellus hair follicles on womens' faces and are all associated with sebaceous glands.
The epidermis consists of several layers and varies in surface topography and thickness. The epidermis on the soles of the feet and palms of the hands is thickened; on the scalp and face it is less thick, while on the trunk and the interior surface of the limbs it is thin.
Stratum corneum The outermost layer of the epidermis is the stratum corneum. This is the visible layer, and the one on which cosmetic chemists focus most attention. It consists of about 15 to 20 layers of flattened cells (eratinocyles). which become disassociated and ready for shedding or desquamation as they migrate to the surface. These cells are distinguished by not having nuclei or normal cell contents, and were thought to be dead, but they do have function and organization, and they can be controlled and managed.
Stratum granulosum The next layer within the epidermis is the stratum granulosum or granular layer. As cells progress to the surface, they form the characteristic granules of this layer.
Stratum spinosum Beneath the stratum granuosum is the stratum spinosum or spiny layer. This layer of cells is distinguished by a spiny appearance and the presence of desmosomes. This is the area where the intercellular lipid is formed. This lipid material is extruded between the cells of the stratum corneum as they migrate to the surface. The cells are looked upon as bricks, and the epidermal lipids as the mortar which helps hold the cells together. The lipids are similar to sebum, except for a lack of wax esters and squalene, and the presence of ceramides.
Stratum basale This is the innermost layer of the epidermis and is also known as the germinative layer. It is in contact with the dermis. It is in this layer that epidermal cells originate through the formal ion of keratinocytes, which differentiate as they migrate to the surface. This layer also produces langerhans cells, which play a role in the immune system and the body's defense mechanisms. The entire cycle of formation, differentiation, migration and exfoliation irorn stratumbasale to shedding by the stratum corneum takes from 40 to 75 days. The stratum corneum cycle is about one third that of the total epidermis.
The epidermis is dependent on the dermis for its source of nutrition. The dermis is a connective tissue that provides a support system for the epidermis. All of the skin's blood, nerves, lymph and external structures, such as hair follicle with sebaceous glands, and eccrine and apocrine sweat glands, are based in the dermis.
Fibroblasts, collagen and elastin The dermis has a fibrous component of various identifiable materials. The primary fibrous material is collagen, with a lesser content of elastin and smaller proportions of other fibrous structures. These fiber bundles and structures form an interwoven network that lends support, flexibility and suppleness to the skin. The source of these fibrous materials, the fibroblast, is the most numerous type of cell in the dermis.
Mast cells Mast cells are the second most numerous cells in the dermis. They are granular in nature and are most numerous near the capillaries. Mast cells participate in the release of enzymes and materials to control function or respond to injury.
Blood supply The blood supply for the dermis is abundant and consists of a complex of arterioles and capillaries that are drained by the venous system. The blood supply does not extend into the dermis. The purpose of this complex network is not only for cellular nourishment, but also for temperature control, as demonstrated by flushing (dilation) and goose bumps (constriction) at opposite extremes of the body's temperature control.
Hair follicles and sebaceous glands The combination of hairs, and their follicles and attendant sebaceous glands is known as the pilosebaceous system. The hair follicle consists of epidermal tissue that extends into the dermis for its biological needs. There it obtains a source of nourishment from an abundant supply of blood, attaches to nerves and in the case of large terminal hairs, has an attachment to the arrectores pilorum muscle. This muscle can raise hairs in response to cold, or emotional signals.
In general, a sebaceous gland is associated with a hair follicle. For the purpose of this review, the activity of the sebaceous gland, and not the hair, will be focused on. The majority of sebaceous glands occur on the head and upper torso of the body, and are only absent from the palms and soles of the feet. Most sebaceous glands associated with hair follicles open inside the pilosebaeous canal. On the face, some large sebaceous glands either associated with fine velus hairs, or without hairs, can open directly on to the surface of the skin. The sebaceous glands form and secrete sebum, a unique blend of lipid materials not found anywhere else in the body. The size, maturity and amount of secretion is triggered by hormonal activity, which peaks in the teen age years. Sebum is synthesized within the sebaceous gland and consists of triglycerides. fatty acids, wax esters, squalene, and cholesterol esters. The sebaceous glands, when active, produce a continuous now of secretion without regard to the condition of the skin and hair, or the level of previously secreted sebum on the surface.
The sebaceous glands are a site for the development of acne. Even although the glands are controlled and enlarge and develop by hormonal activity within the body, acne is dependent on many other factors beyond the development activity of the glands. This will be discussed later.
Sweat glands Two types of sweat glands are present in the human (6). The most prevalent (more than two million] are the eccrine sweat glands, which have a primary function of controlling body temperature. The eccrine glands are also responsive to other triggers such as stress and sunlight. They extend from the epidermis into the dermis and. in the dermis, are surrounded by blood vessels. The sweat secreted by the eccrine system is relatively low in solids, consisting primarily of sodium chloride.
The apocrine glands are found primarily under the arms and associated with the sex organs. They are, like the sebaceous glands, primarily associated with hair folllicle, usually opening into the pilosebaceous canal. These glands are much larger than eccrine glands but. like eccrine glands, originate in the dermis. The sweat produced, much less in quantity than that produced by eccrine glands, is higher in solids and of a more complex nature. It is viscous and milky, and contains high levels of protein, along with cholesterol, steroids and other lipids. It does not have a pronounced odor on secretion, but develops a distinctive odor due to enzymatic activity on the skin. The purpose of aprocrine glands is unknown, but has been speculated to be sexrelated, or a means of identification of communication through odor. This is the function of similar glands in other mammals.
The colour of the skin and hair is primarily due to the existence of pigment bodies known as melanin. Melanin is produced by the melanocyte cells present in the stratum basale. These melanocytes are present in this basal layer in great abundance and the number does not differ greatly in people with more or less melanin pigment or colour in their skin. Melanin may be produced in either a yellow/red or black/brown colour, and the colour of the skin is determined by the amount and type of melanin produced. Melanin production is increased by exposure to the sun and plays a role in protecting the skin from sunlight.
In addition to a basic understanding of the anatomy and function of the skin, a good foundation and understanding of various tests available for the function of the skin, as well as tests for product performance, is essential. The cosmetic chemist has been aided by many new test methods to help determine performance of skin-care products. These methods vary from in vivo observational or instrumental test methods to a wide variety of in vitro test methods.
The majority of skin-care products are sold to improve the appearance and feel of the skin, and are broadly classified as moisturizers. The condition and appearance of the skin is a function of its softness and flexibility, which is adversely affected by loss of water. Tests for moisture content and moisture transmission, as well as the viscoelastic response, ultrasound techniques, and elecirical properties of skin have been the subject of much study, with the development of increasingly sophisticated instrumentation to show the condition of the skin and its water content. Most of these new methods have evolved to help evaluate the potential performance of products, and are very useful in screening formulations, levels of ingredients and other stepwise formula variables. However, experience has shown that none of the available test methods totally replace in vivo application, professional observation and sophisticated consumer research utilizing both professional, and self- or consumer- evaluation of performance.
In vivo observational tests for moisturizers One of the primary and most valuable in vivo tests used, especially to test hand and body lotions, is the regression test method developed by Kligman . This test is run in a location where the ambient relative humidity is conducive to development of dry skin. Panelists are 'dried down' by washing with a non-fatted bar soap for one week, without use of a moisturizer on the test site, which is either hands or lower lateral legs. The hands or legs are then observed and graded. The test protocol calls for use of product by some panelists, with others acting as non-treatment controls. At various times, during a two-week period, the condition of the skin is evaluated for dryness. flaking and redness. Treatment is then withheld for one week, and the rate of return to a dry condition is observed. This testing yields a good evaluation of the treatment potential moisturizer products and their duration under severe conditions. The method has recently been improved as reported by Boisits et al.
The condition of the face and its response to moisturizer products have also been evaluated by a variety of methods. A widely used methods is the superficial facial line test, developed by Packmanand Cans. This test has been developed for use by trained judges and also by untrained panelists. The standard method utilizes scoring, by trained judges, of superficial facial lines for depth of line in each of four areas in a half-face study. The other half of the face as a non-treatment contrl. Four days long, with no treatment on the first day and treatment twice a day on days 2,3 and 4. The authors also discuss the use of self-evaluation by twelve untrained evaluators, who evaluate superficial facial lines in a similar test method.
Cell turnover testing. A very useful test to determine cell turnover rate utilizes the dansyl chloride test , in which dansyl chloride, which fluoresces under a long-wave UV or Woods lamp, is applied to the skin. This material penetrates the stratum corneum to a uniform depth. The cell turnover rate, or transit time, is determined by disappearance of the stain compared to a non-treatment site.
In vivo instrumental tests An in vivo instrumental test that is proving to be of great value is profilometry, which is especially useful in the assessment of the changes to the skin's surface caused by the anti-ageing effect of retinoid therapy on sun damaged skin. Two primary methods are used in profilometry. One method employs replicas and the other uses photographs. Fully hydrated skins such as altered surface characteristics, as measured by both lower peaks and greater distance between peaks. This is also the case with skin that has fewer lines and wrinkles clue to effects other than hydration. In evaluation with a replica, an instrument with a stylus produces a tracing of the topography of the skin, based on a replica produced by denial impression material. With two-dimensional photographs, computerised image analysis techniques are used to review the image.
The gas-bearing electrodynamometer (GBE), has been widely used to evaluate the viscoelastic properties of the stratum corneum. both in vivo and in vitro. More recently computer handling of data generated by this device has improved its utility. The Twistometer device measures resistance to torsion of the skin, as applied by a rotating disc inside an external ring, which acts as a staler. This device is used to evaluate the skin's softness and suppleness. There has been a long history of the measurement of not only the water content of skin, but also the flow of moisture from the skin, which is known as moisture vapour transmission rate (MVTR) or the moisture/water loss or transepidermal moisture loss (TEML). MVTR is a technique that has shown continual refinement. Early papers by Berbe and co-workers outlined theory and practice. Progress has continued to the more recent development of a well-accepted instrument, the Servo-MedÂ® evaporimeter. Most of the work on the direct measurement of water content in skin has utilized an infrared (IR) spectrophotometer. An excellent review is given by Potts.
In vitro testing for moisturizers Many in vitro tests are cited in the literature. An excellent overall review covering both in vivo and in vitro techniques has been written by Salter. A technique for conducting the in vitro moisture vapour transmission rate was usefully outlined by Reiger and Deem. Measurement of occlusivity by these technique is useful and, in general, quite reproducible. The tests consist of the flow of moisture through a barrier, which is often a synthetic film with a transmission rate similar to that of skin. This technique (MVTR) combined with a water-holding technique to measure hydration, or the ability of (he formula or test material to maintain humectancy, is very useful in evaluating of predicting potential in vivo results.
Test methods other than MVTR and water holding capacity have been outlined by Quattrone and Laden . They include scanning colorimetric techniques, scanning electron microscopy (SEM) and biomechanical properties of skin under in vitro conditions. In vitro test methods can be instructive when their correlation to in vivo performance has been established. In the author's experience, a battery of tests and an excellent history of correlation are necessary for the tests to be of predictive clinical value. The problem is that, when in vitro tests are used with excised skin or a synthetic membrane, un-like the human skin, there is a lack of the biological underpinnings of the epidermis, which is anything but an inert, static or dead layer.
In vivo test for sebum An in vivo device for measuring the oiliness of the skin has been developed. This device (Sebutape) is a film that visualizes and traps sebum. The tape can then be analyzed, and total relative sebum amount computed using image analysis. If quantification is not the only requirement, the sebum can be solvent-extracted, gravimetrically analyzed and broken down into component parts. This can be a very useful technique for assessing the instant removal of sebum by cleansers, or the effect on sebum production of various treatments.
In vivo test for cleanser mildness A wide variety of cleansers are available on the market and will be covered within this chapter. Tests for cleansers have focused primarily on testing soap or detergent for-mulations for mildness. In the past, mildness has been evaluated by the Soap Chamber Test. In this test, diute solutions of soaps or test solutions are maintained in a cup held against the skin of human volunteers. The skin is then evaluated for redness, scaling, and fissuring, often against high irrilancy (non-fatted soap bar) and low irritancy (fatted sodiumcocoisethionate bar) controls. A more recent modification of this method calls for a shorter test, and measures the increase in MVTR by a Servo-MedÂ® evaporimetcr. This has shown a close correlation with the longer duration visual assessment technique. The: authors of the Soap Chamber Test cautioned as to the limitations of the test and recommended, in addition to this method, the use of ex-aggerated washing tests, commonly known as forearm wash tests. These methods differ from the Soap Chamber Test in that the Forearm Test adjusts frequency for humidity, while the Flex Test is reported to be unaffected by humidity. For evaluation of facial cleansers of all types for mildness and drying potential, the method outlined by Frosch utilizes half-face testing with realistic use conditions. In order to obtain suitable dryness scores, this lest is best run during periods of low relative humidity. Cleanser tests for efficacy, evaluating soil and make-up removal, as well as esthetic properties and after-cleansing skin-feel, must also be done to obtain a complete picture.
A combination of all these test methods, together with adequate clinical and consumer trial and observation, should enable one to have a great insight not only into the performance of products but, more importantly, as to how and any why products work, and how variations in formula affect performance. This is necessary for the enlightened formula lor.
Throughout the remainder of this chapter, formulas will be pre-sented as examples of particular formulation categories. These will be prototypical examples, taken from experience or from suppliers. They are only intended to give the formulator a general idea of typical formulas and constituents by category, and are neither tested for per-formance or stability, nor ready for the market. This would require considerable experimental work and testing. In addition, many new raw materials with functional and emotive benefits are available from raw material suppliers and should be reviewed on an ongoing basis during development.
Formulation is an art and a science, and requires close attention to detail and trial and error before proficiency becomes routine. The formulator must, first of all, make a product that has characteristics required by the ultimate consumer of the product. These requirements will vary depending on the specific usage, demographics of the consumer, expectations, claims, class of trade and packaging. The formula must be fit for use by the consumer at any point during its expected shelf-life. During formulation, this requires adequate stability trials and examination for microbiological integrity. It must also be possible to make the product using reasonable manufacturing equipment on a scale that is appropriate for anticipated demand. Further areas that are becoming increasingly important are safety under all conditions of use and potential misuse, and regulatory and environmental acceptability. These aspects of formulation will be discussed in the following sections.
Much formula information, from a variety of sources, is available to the cosmetic chemist. Excellent background information and general formulation information may be obtained from the several reference books kept in most industrial libraries or large public libraries. The nature of these texts will generally give excellent historical data, but, the most up-to-date formulation data can be found from other sources. The first of these are the many periodicals that are published for the technologist in the cosmetic industry. These periodicals often have formulation articles and review articles covering a specific category, and also provide another valuable resource, i.e. identification of, and advertising from raw material suppliers. Raw material suppliers frequently publish information on starting formulas and give specific help with formulating. They are a rich source of ideas and guidance and some will even provide formulation assistance in their own laboratories. One must keep in mind, however, that the goal of the supplier is to sell the raw material.
An excellent starting point for the formulator is to review listed ingredients on the labels of finished formulas of market leaders' target products sold where ingredient disclosure is required, such as in the US where all cosmetic products must list all ingredients in descending order of content. It is helpful to review these ingredient lists, perhaps assay for a material or two. and speculate on the formula based on other sources of starting formulas. An assay for water, total lipid material and, if incorporated, humectant. will give much information about a formula that has already proven to be acceptable to consumers. The ingredient list in the US also uses accepted nomenclature from the US trade association, the Cosmetic Toiletry and Fragrance Association (CTFA) in its Cosmetic Ingredient Dictionary. This in excellent reference, as it lists not only the generic CTFA name, but provides technical information on the raw material, and lists suppliers of it. Another good source of information is to join and participate in local cosmetic chemists' organizations and attend their meetings. Seminars are held frequently and are attended by suppliers to the industry.
Consumer testing and input is a must for the formulator. This should take place before and after product development. Once a prototype formulation has been developed, determined safe for use by consumers, and adequately preserved, it should undergo initial testing for consumer acceptance. Most commercial organisations have standards for consumer testing, which are usually organized by the marketing department. It is, however, very helpful to the formulator to seek consumer input at all stages during development of a product, for instance to develop an enlightened view of consumer requirements by talking to target consumers about their needs before development is initiated. This can be done informally or formally, either one-to-one, or with groups of consumers. Another useful technique is to give representative consumer users and non-users of the leading product in a category, an unidentified sample of the market leader to use for a week. Following this, the way in which the consumers used the product, the results of product use, and the likes and dislikes can be discussed on an open ended basis. Attribute comments and areas of dis-satisfaction with the target product should be noted. The information can then be used as a base line for later examination of a developed prototype. Another useful technique, known as a sequential monadic. is, at the next stage of development, to have target consumers use both the prototype formula and the market leader of competitive bench-mark product. Half the panel first uses the prototype for a period of time, and then uses the competitive benchmark product or market leader: the rest of the panel uses the products in reverse order. With this technique, a good comparison of the prototypes performance versus the benchmark product on attribute by attribute basis is obtained. At this stage, testing should be on an unidentified basis, since the requirement is for performance and attribute data as a guide to formulation. In larger concerns, testing of finished products on an identified basis with advertising or concept, is usually handled by the marketing or market research department. It is possible, however, for the cosmetic chemist formulator to have this work done for them by independent market research firms, or by advertising agencies.
Stability testing is done to ensure that a developed product will be fit for use during its expected life. Stability testing should be done early in the development cycle to remedy any problems before final testing. A well-run stability trail can provide much information about a product in a relatively short period of time. Prototype products in packaging, representing the ultimate trade package material, can be placed at ambient, and elevated (e.g. 37Â°C and 45Â°C) temperatures, refrigerated and cycled through freeze/thaw cycles, and placed in high humidity chambers. During these trials, testing should focus on attributes most important to the product's performance, or on the integrity of any active ingredients. In addition, there should be physical testing, for example pH and viscosity, chemical content of active ingredients, water content, etc. The formulator must not overlook attributes relating to consumer perception, such as fragrance, colour, rub-in characteristics and appearance. Two or three months of successful elevated temperature testing and three or four freeze/thaw cycles will usually indicate that products will have an adequate shelf-life. It is important, however, to continue testing for longer periods at ambient temperature, to obtain an understanding of the product's ultimate shelf-life. Further testing whenever changes are made to the supply of raw materials or to the formulation is essential.
During the development phase, close attention should be paid to the microbiological integrity of the formulation. Professional advice should be sought from a well-trained industrial microbiologist. If this is not immediately available, input and guidance on preservatives from the suppliers' staff and consultants should be sought. Suppliers will often have more than one preservative and can make recommendations about particular types of formulation. Another method of finding appropriate preservatives is to review ingredient labelling on similar types of products that are available from reputable manufacturers and which have similar constituents, pH and package types. This, coupled with a microbiologist's or a preservative vendor's input can often give several trial systems. Finished products are usually tested using a challenge technique. If this essential testing is not available in-house, a qualified contract lab can assist. The test involves adding large numbers of a variety of organisms to the product and checking the ability of the product to reduce them to an acceptable level. To ensure that the product retains its ability to remain preserved, adequacy of preservation should also be checked during stability testing.
A product cannot be a commercial success unless it can be made with large-scale equipment, therefore as soon as a prototype develops beyond its earliest stages, and at all subsequent stages of development, manufacturing should be considered. If an engineering group is available, it should be consulted, and should participate in a laboratory batch of the new product on a bench scale. This, if possible, should compare the compounding of the product, heating and cooling cycles, phase additions, etc., with a similar type of product that is already being manufactured. Any significant deviations from norm should be noted and investigated for possible change or for special attention during scale-up. Scale-up can represent large changes in batching times, time at temperature, etc. It is advisable to scale-up in increments, preferably not greater than 10 x at any stage. For instance, going from a 1 kg lab batch to a 10 kg lab batch, then to a 100 kg pilot batch and 1000 kg manufacturing batch would be a logical sequence. Any significant problem at each stage should be investigated and, at the very least, abbreviated stabilities should be run with product from each stage.
When final manufacturing is initiated, the development chemist or engineer should stay with the process until several batches have been made without problem. It is helpful, during the life of the product, to return to manufacturing and continuously improve the process. Time should be spent with veteran compounders, as they often have great insight into how a process can be improved. Product from first production trials should also be put through a complete stability test, comparing results to those obtained during development, and addressing any problems that may occur.
The product must be safe under all conditions of use and potential misuse. Safe products arise from a combination of careful formulating, good background data and adequate testing. A review of materials used in products for similar purposes is an excellent place to start. Most successful commercial products have been adequately tested and have a history of safe usage. Safety data for each raw material should be available from its manufacturer and should be reviewed. In the US, the CTFA has a Cosmetic Ingredient Review, which evaluates materials and also lists safety data for materials that have been reviewed. After a thorough background check, finished produces should be tested through a competent third party. Many testing companies not only do safety testing, but also recommend appropriate testing that should be done for the class of product that has been developed. It is often useful to solicit testing protocols from two testing companies, asking them to explain and justify each test they recommend. It must be remembered, however, that they can only make enlightened recommendations based on input. Divulging as much information as possible at this stage, will give better, more appropriate testing input, and insight into possible untoward reaction.
After adequate clinical testing has been completed, and during all stages of consumer trial, it is important to check for unexpected reactions or patterns of misuse, while carefully extending exposure. Careful attention should be paid to reported reactions from usage or misusage situations. After launch, there should be mechanism to check on reported reactions to determine if, on a broad exposure, these levels are higher than one would expect for the category, category adverse response reporting data is available from the US Food and Drug Administration (FDA), and often from local trade associations.
Regulatory and Environmental Requirements
Regulatory requirements vary greatly from country and can be ascertained by direct contact with the local regulatory authority. Excellent advice can frequently be obtained from local trade a associations, who have insight into not only what is required by law or regulation, but also what is acceptable and expected. Membership of trade associations and participation in their activities is invaluable.
Environmental restrictions or concerns are often more elusive, or more difficult to determine. Trade associations, trade publications and local groups of cosmetic chemists can be of great help. Many companies also seek advice from consultants who are experts in this area, or, in some cases, have direct meetings and constructive dialogue with leading environmental groups. The person responsible for developing a product or formula should accept total responsibility for the product, and care and diligence should be exercised throughout every aspect of product development.
Skin cleansers constitute an important segment of the skin-care market. Cosmetic chemists are usually involved in the facial cleansers in forms other than bars. This, however, overlooks a large portion not only of the overall market, but also of consumer's usage patterns. Most consumers use bar products, either based on soap or synthetic detergent (syndet), for skin cleansing. All other cleanser products represent other types of usage and vary greatly from market to market depending on patterns of make-up usage, cleansing habits, etc.
In order to properly classify cleansers, it may be helpful to put them on a grid, roughly related to their physical nature, chemistry and functionality, and ranging from products that are anhydrous oils, at one end of the spectrum, to soap and water at the other (Table 1). Various product types have different functions and, while they have advantages for a specific condition or soil, none is universal. Most consumers use more than one type of cleanser, so an understanding not only of chemistry and formulation, but also of consumer usage patterns for their needs in a specific market or market segment, is key.
When classifying cleansers, the various soils on the skin must be considered. Soils come from a variety of sources, but can be classified broadly as oil-soluble, water-soluble and insoluble. Sources for oil-soluble soils can be sebum, residue from moisturizers, or waterproof make-ups. Water-soluble materials may also be residue from make-up or moisturizers, soluble skin oils, soils, and soluble grime. Insoluble materials are represented by dead cellular matter, make-up pigments or, in hard-water areas, precipitated metallic soaps.
Anhydrous Oily Cleansers
The first category of cleansers is the most oleophilic group. Mineral oil, petroleum jelly, vegetable oils and esters are useful as non-drying skin cleansers for removal of waterproof make-up and oils-soluble soils. The disadvantage of these cleansers is that they are not readily rinsible and often have poor cosmetic and esthetic characteristics. More modern versions incorporate moderate to high levels of esters or gentle oil-soluble surfactant materials to make the products Jess greasy, more pleasant and, in some cases, rinsible. In addition, some formulations are thickened to form gels, which are easier to spread on to the skin and can be tissued off.
Water-in-Oil Emulsions: Cold Creams
The next category of products are water-in-oil (W/O) emulsion cream and lotion formulas, typified by cold cream. Cold creams are referred to as W/O emulsions but, during processing and usage, are more complex water-in-oil-water (W/O/W) emulsions, or mixed emulsions. The partial or mixed external oil phase of these mineral oil/ bees wax/borax systems dissolve oil-soluble materials and, because of the oily external phase and the beeswax/borax soap at the interface, they are able to solubilize, wet out and transport soil and waterproof make-up. Cold creams are generally not rinsible, are considered greasy and inelegant, and are tissued off the skin. They leave behind a film that has proven moisturizing characteristics. Classical cold cream formulas set the standard for mildness to skin and eyes. In recent years, some rinsible cold creams have emerged. These are cold cream and similar bases to which non-ionic emulsifiers have been added with an increased water phase. These rinsible systems then become oil-in-water (O/W) emulsions. They are not as satisfactory for a waterproof make-up removal, but are rinsible and more cosmetically elegant.
Procedure: Reduce the cetyl esters wax and the white wax to small pieces, melt them on a steam bath, add the mineral oil, and continue heating until the temperature of the mixture reaches 70Â°C. Dissolve the sodium borate in the purified water, warmed to 70Â°C, and gradually add the warm solution to the melted mixture, stirring rapidly and continuously until it has congealed. Pour into jars 50Â°C and cool.
Oil-in-Water Emulsions: Cleansing Milks
Non-foaming O/W emulsions with greater than 50% water phase typify the next category of cleansers. These products are typically referred to as cosmetic milks. The primary cleanser and emulsifier is often a TEA*/fatty acid soap, or a detergent such as sodium cocoylisethionate supplemented by anionic or non-ionic emulsifiers. Cosmetic milks are skin-friendly and have many similarities with O/W moisturizing lotions. However, they differ from moisturizing lotions in that they generally have less water in the water phase, excess TEA fatty acid, and higher levels of a secondary emulsifier such as self-emulsifying glycerol monosterate. Significant levels of mineral oils or esters may also be incorporated to ensure adequate levels of solubilization of oily materials without reducing rinsibility.
TEA. triethanolamine; EDTA. ethylene diamine tetraacetate; MEA, mono ethanolamide; PEG, polyethylene glycol; POE, polyoxyethylene.
Procedure: Dissolve xantham gum in water; heat to 65Â°C. Add sodium cocoyl isethionate, preservative, and EDTA. Premix part B and heat to 65Â°C. Add B to A with good mixing: then cool to 45Â°C. Add fragrance
Fatted Mild Syndet Foaming Bars and Cleaners
The next category is differentiated because of a foaming characteristic. This is the category of fatted syndet bars and gentle fatted foaming pastes and lotions. These products have good wetting properties but, when used in soap chamber or flex washing studies, are significantly more gentle than fatted soaps, detergent solutions or non-fatted soaps. They occur as bars (fatted sodium coco isethionate, as pastes based on fatted built mono alkyl-phosphates. and as pastes and lotions based on fatted and built sodium coco isethionate. Recent additions to this range of gentle foaming cleansers have been lotions based on sarcosanate surfactants, with high levels of glycerol. protein, and fatty materials to ensure a mild effect. Due to their gentle nature on the skin, mild bars, foaming pastes, and lotions are becoming more important on a world-wide basis.
Procedure: Disperse the hydroxypropyl methylcellulose in water. With mixing, add the triethanolamine to initiate hydration. Begin heating to 65Â°C. Add the part B ingredients. Premix part C; heal to 65Â°C. Add part C to the batch with good mixing. Cool to 45Â°C; arid fragrance.
Super Fatted Bar Soaps
Fatted bar soaps have greater cleansing characteristics, with iess skin residue than fatted and build mild detergent pastes and lotions. The formulations contain varying amounts of falty acids or other fatty or moisturizing materials to decrease their aggressive behaviour on the skin. This results in a non-taut skin-feel upon rinsing, and less damage to the skin.
Procedure: Blend all ingredients in an amalgamator. Refine, extrude and stamp bars.
Astringents and toners are a class of skin cleansers that have a special use and very specific formulations. They are hydroalcoholic solutions with an alcohol content from 20-70%. The products with lower levels of alcohol are developed for sensitive skins, while those with higher amounts are for oily skins. Astringents and toners often contain small amounts of emollients or humectants to decrease their defatting of the skin. They are generally used by oily-skinned consumers or teenagers as a supplement for cleansing and acne treatment. They are often the last cleansing step in a ritual to make to make the skin very clean in a preparation for the use of a moisturizer.
Procedure: Dissolve menthol in alcohol. Add fragrance, water and other ingredients. Blend at room temperature.
The final category in Table 1 consists of the minimally fatted or non-fatted bar soaps. These coco/tallow soaps are excellent cleansers, but can, if used excessively, irritate the skin. They enjoy considerable usage among consumers as part of an everyday cleansing ritual and, on a worldwide basis, are the most commonly used cleanser product.
Procedure: Blend all ingredients in amalgamator. Refine, extrude and stamp bars.
A speciality category not shown in Table 1 is the creams, which contain particulate materials. These products are often O/W emulsions (if non-foaming) or gentle pastes (if foaming). They contain particles of polyethylene or other inert materials such as ground seed-husks. The purpose of these paniculate materials is to remove loose flakes of stratum corneum and to polish the sin. Interesting research by Loden and Bengtsson indicated that the effect of scrubbing with a particular scrub can be helpful if there is a need to remove a layer of stratum corneum. However, excessive use should be cautioned as, due to their mechanical action, they can be irritating.
Procedure:Heat A to 70Â°C. Meat part B to 75Â°C. Add part B to part A with agitation and cool to 40Â°C. Add part C and mix thoroughly.
The selection of cleansers and their constituents requires extensive testing to ensure suitability for use. The Coal should be to remove soils and make-up with minimal damage to the skin. An interesting approach to the selection of surfactant materials and products is out-lined by Komp, utilizing the Duhring Chamber Test, as well as the antecubital washing test. As well as these exaggerated tests, it is very important to follow prototype formulation with controlled in-use testing for soil and make-up removal, and consumer evaluation use testing.
Moisturizers are products that, are usually emulsions, either O/W or W/O. There are two principal forms of these products: (i) semi-solid emulsions, known as creams: and (ii) flowable emulsions, known as lotions. Moisturizing products are differentiated not only their emulsion type and/or physical form, but also by their functional use. For the purpose of this discussion, all-purpose creams, hand and body lotions and creams, facial moisturizing lotions, and facial 'night' creams. will be considered.
The purpose of moisturizing products is to restore and maintain the skin in a good-looking, fully moisturized condition. To maintain this condition, the stratum corneum must be in a fully hydrated condition that allows flexibility and elasticity. Early work by Middleton and Alien and a review by Idson, show the relationship between water content in the skin, as affected by the temperature and humidity. In most products, this moisturization is accomplished by a combination of hydrating by water followed by the actions of occlusives and humectants. Emulsion products of either O/W or W/O break down when rubbed out on the skin, and add water from their own composition to the surface layers of the stratum corneum. This hydrating effect by water accounts for the instant appearance benefits, including reduction of visible dryflakes and chapping. Less-immediate ef-fects occur through occlusivity and humectancy.
Occlusivity occurs when the transepidermal water loss is slowed through reduction of the moisture vapor transmission rate. Many fatty materials reduce the MVTR. Typical of these materials would be petroleum jelly, mineral oil. vegetable oil, silicone oils, waxes, fatty acids, alcohols, and esters of mineral, animal or plant origin, as well as many synthetic oily materials that are available to the cosmetic chemist.
Humectancy is a separate but related phenomenon, in which materials that have an affinity for water: (i) help bind water to the skin; (ii) resist evaporation from the skin: or (iii) under certain circumstances. attract water to the skin.
Typical of these materials are glycerin, sorbitol, sodium lactate and sodium pyrollidone carboxylate (the skin's naturally occurring humectant. Such humectants have been shown to be valuable not only in hydrating the stratum corneum, but also in improving the elastic modulus and stress relaxation modulus, thus altering the viscoelastic behaviour of the stratum corneum. Extensive experimentation with glycerine has shown that it moisturizes dry skin in a dose-related relationship dependent on the concentration of glycerin. It was postulated that the water glycerin mixtures on the skin also assist in plasticizing the stratum corneum in a less than transient manner. Middleton found that lactic acid was absorbed by the stratum corneum and that increased extensibility was retained by the stratum corneum.
All purpose creams are typified by a VV/O emulsion or by high oil content O/W emulsions. These products are for general face and body usage and generally have a heavy consistency and significant drag on rub-out. In addition, a small amount of product is able to cover a large area. Many all-purpose creams contain from 30-70% oil phase, resist wash-off, and are excellent protective as well as treatment products. They represent a very significant percentage of the European mass moisturizer market, and are often sold in flat packs (tins) or tubes. Performance characteristics and testing should focus on tests to maximize a reduction in the MVTR, resistance to wash-off and a prolonged improvement to the skin, as demonstrated by regression analysis. Lighter weight, more modern products are, however becoming popular.
Procedure: Heat part A and B to 70Â°C. Add part B to part A. mixing continuously. Mix and cool to 35-40Â°c and add part C. Continue mixing until dispersion is complete. Adjust evaporation losses with water.
Procedure: Heat parts A and B separately to 70Â°C. Add part A to part B with good agitation. Mix to 35Â°C and add part C. Continue mixing until dispersion is complete.
Hand and Body Lotions
Hand and body lotions are generally O/W emulsions, with typical lotion products containing 10--15% oil phase, 5-10% humectant, and 75-85% water phase. They are characterized by easy flow and pumpabilily. fast rub-in, and a lack of stickiness after rub-in. Most of these products are sold in bottles with or without pumps, or in tubes. Their primary performance characteristics are their ability to instantly hydrate skin and to relieve dry skin symptoms. In addition, they should have excellent profiles in MVTR reduction and prolonged improvement to the skin as shown by regression analysis.
Procedure: Heat parts A and B separately to 70Â°C. Add part A to part B with good agitation. Mix to 35Â°C and add part C. Continue mixing until dispersion is complete.
Hand and Body Creams
Most modern hand and body creams are O/W emulsions with greater levels of oil phase and possibly higher humecant levels than lotion products. They generally contain 15-40% phase and from 5-15% humectant phase. These products are easy to apply have a reasonably fast rub-in, good esthetics, and often resist wash-of. They are typically sold in jars or tubes. Their performance characteristics are similar to hand and body lotions, often with the added benefit of more resistance to wash-off.
Procedure: Heat parts A and B separately to 70Â°C. Add part A to part B with good agitation. Mix to 35 C and add part C. Continue mixing until dispersion is complete.
Facial Moisturizer Lotions
In terms of esthetics, facial moisturizer lotions are very different from hand and body lotions. They contain occlusive agents and humectants at the lower concentration levels of hand and body lotion formulations. Great attention is paid to quick-breaking, instant-ab-sorbing products with no greasy after-feel. These effects are obatined by the use of emulsions that break down quickly, dry to a matte finish, and prize light emollients such as esters and fatty alcohols and, where appropriate additives such as volatile silicones. Performance characteristics are good moisturizing capability, the ability to reduce MVYTR rates, and also an immediate and a short-duration effect on superficial facial lines. Visual peformance effects and esthetics are key factors in successful products.
Procedure: Mix all of part A except the triethanoamine. After all of part A is dispersed add TEA. Heat parts A and B to 70Â°C. Add part B to part A with good agitation. Mix to 35Â°C and add part C. Continue mixing until dispersion is complete.
Facial Moisturizer Creams: Night Creams
Facial moisturizer creams are often sold as night creams or heavier duty moisturizer products than their lotion counterparts. They generally have higher levels of occlusive and humectant materials (nan facial moisturizer lotions, but are formulated (with esthetics as a principal factor) using lighter emollients, quick-breaking emulsions, and controlled levels of humectant materials. Additives such as volatile silicones are often added to improve rub-in, break and a non-greasy after feel which, together with a matte finish, are key esthetic features. Performance characteristics are excellent moisturizing capabilities and a good effect on superficial facial lines.
Procedure: Heat parts A and B separately to 70Â°C. Add part A to part B with good agitation. Mix to 35Â°C and add part C. Continue mixing until dispersion is complele.
The emergence of new technology with proven performance to reserve damage from photoageing necessitates a separate section on anti-ageing products. Many such products are sold, but prior to discovery by Kligman of the effect of retinoic acid on photodamage. and patents issued to Van Scott and Yu on a-hydroxy acids, these products had primarily cosmetic benefits: that is. complete hydration of the skin, a return of suppleness, the reduction of superficial facial lines and. at times, a masking effect, givng lines a more youthful, albeit, transient. improved appearance.
Ageing is well understood and. although much can be done in the laboratory to affect cellular vitality. or to affect the overall longevity of laboratory animals, the human species has not materially advanced in its maximum age as proposed in the original theories of Hayflick and Moorehead. A more optimistic review by Puglese, both of ageing and of events within overall cellular mortality, is of interest and suggests that a proper understanding of the entire ageing process is the key to effecting changes in it. This review offers many areas of interest to the cosmetic chemist. Ageing results in subtle and not so subtle changes in the appearance of the skin. It is probable that many of the effects seen on the skin with ageing are an indirect result of the decrease in the blood supply to the dermis. The number of sebaceous ducts and the level of secretion from them also decreases, however, many of the remaining ducts increase in size. An excellent review of these changes in physiology and pathophysiology by Gilchrest is worth reading in order to understand the substrate in question.
Manifestations of ageing that are of primary concern to the cosmetic chemist are wrinkles. These lines, which become more pronounced with age, especially on the face, are caused by a shrinking of the superficial muscles which have their points of insertion in thedermis. The facial exprssion muscles are the first areas to change with age. They also develop the deepest wrinkles. As they lose superficial mass, thinning of the epidermis and a loss of collagen and elastin are apparent. These all contribute to the visible process called ageing. As yet, it has not been possible to affect this frank, deep cellular ageing. One reason is that there is nothing histological to differentiate the cellular structure of a wrinkle from that of a non-wrinkled epidermal area. An excellent review on this entire subject is provided by Wright and Shellow, who studied the histology of deep wrinkles and adjacent non-wrinkle areas.
Advances are continually being made to show improvements in ageing of photodamaged skin, due to retinoid and retinoid-like effect, more recently demonstrated by a-hydroxy acids and related compounds. Several natural physiological vitamin A or retinoid effects that are known to be ongoing in the dermis are dermal deveopment, collagen synthesis, hyaluronic acid synthesis, DNA content and epidermal protein expression. Since these factors are in part, controlled by vitamin A and its derivatives in healthy skin, it has proven worthwhile to seek profound effects such as those demonstrated by topical treatment of retinoic acid. Achieving a retinoid effect is not possible by simply adding vitamin A or another retinoid to a cosmetic formula. Followng topical application, the effective drug must be available to the dermis and epidermis, without untoward side effects. Recent work with the hairless mouse model has correlated a dose response to increasing levels of retinyl palmilate in a suitable cosmetic preparation. This response from topical treatment resulted in an increase in protein and collagen synthesis, and in DNA content, together with a thickening of the epidermis. Prior work with a topically applied retinoid has shown accelerated dermal repair to UV damaged dermis, due to increasing regeneration of connective tissue. Emerging work has shown quantifiable effects on human photodamaged skin, and significant biochemical changes in the hairless mouse model, due to topical application of a common cosmetic retinoid. This, coupled with the ability to increase cell turnover from use of a cosmetic product, the reduction of superficial facial lines through new and improved materials and mechanisms, and the 'plumping' of the epidermis by occlusive of or humectant agents can, in theory be combined to give excellent visual anti-ageing results.
Both Kligman and Van Scott discuss the effect of both retinoids and a-hydroxy acids on photodamage. That photodamage has a profound effect on the appearance of ageing of the skin, is now well understood. Damage that can manifest itself as ageing, stems from the effect on the elastic fibres that provide smoothness and suppleness. Evidence that these changes can be reversed was demonstrated by Kligman et al.
Recently, a-hydroxy acids, primarily lactic and glycolic, have entered the market place in many skin-care preparations. Smith has demonstrated various effects of these materials and has compared their efficacy. Derivatives of a-hydroxy acids have also been marketed.
A growing problem is whether or not retinoid-like materials are drugs. In the US, and increasingly throughout the world, courts and regulatory bodies are telling us that if a product contains a 'drug', it clearly is a 'drug'. Even if it docs not contain what has been previously classified as a drug, but alters the structure or function of the human body, ii may well still be regarded as a drug. In the US. products containing retinoic acid are classified as drugs and are only available on prescription allowed to be used under the supervision of a physician. At the present time, such products are cleared for use only in the treatment of acne, but are being mis-prescribed by many physicians for treatment of photoageing and its associated derma! damage. They are not without side effects, including significant levels of irritation in some patients.
The status of products claimed to possess anti-ageing, and other properties has recently come under scrutiny by the US PDA. The PDA has issued several regulatory letters to companies requesting them to stop making drug chains i.e. "...altering the structure or function of the body." Most of these regulatory letters have been resolved by the companies modifying their claims following negotiations with the PDA. One company has. however, initiated suit over this issue, which will no doubt be decided in the courts. A review of performance claims for skin-care cosmetics, and the basis of US regulations, was written by McNamara . In this review, the legal basis for the distinction between drugs and cosmetics, based on both claims and ingredients, is discussed.
Anti-ageing products have been marketed by the cosmetic industry for many years. Successful new products were often launched by interesting claims such "penetrates 21 cell layers, "speeds up cell turnover" or "enhances overnight repair at a cellular level. However, although these products did have performance characteristics, proven by new biophysical tests that were optimized in the product, they did not truly change the ageing process. The proven ability of retinoic acid to reverse photodamage has now altered this situation, and true pharmacological effect from topically applied products is now a reality. The successful formulator and marketer will have to keep with this rapidly evolving and most exciting area of science.
Sunscreen products form an important sub-class of skin-care products. In order to have a good understanding of these products, the chemist must first understand the physics and pharmacology of solar radiation, and its effect on the body.
Skin damage, and the development of products that help prevent it, require an understanding of the ultraviolet spectrum of light. The ultraviolet spectrum of concern is between 200 and 400 nanometers (nm) and, in practice between 280 and 400 nm. The ozone layer around the earth absorbs the shorter wavelengths, therefore the important wavelengths are UV-B (280-320 nm) and UV-A (320-400 nm). The penetration of the skin by ultraviolet radiation depends on wavelength. As the wavelength increases from 200 to 400 nm, the penetration also increases. Consequently. UV-B penetrates (depending on the thickness of the skin in the area of the body irradiated) into the upper layers of the dermis, whereas the longer wavelengths from UV-A penetrate deeply into the dermis. Due to the variable thickness of the skin on various areas of the body, some areas are more susceptible to sunburn and photodamage (ageing) than other areas.
The immediate symptom of excessive UV-B exposure is sunburn. This is caused by a reaction of UV-B radiation with an absorbing material within cells. This absorbing material has been shown to be DNA, which is then depressed prior to cellular propagation. The ability to penetrate varies greatly according to wavelength, with small percentages of UV-B penetrating to the capillary system in the dermis at lower UV-B wavelengths, compared to roughly 50% at its greatest wavelength (320 nm). UV-B wavelengths, compared to roughly 50% at its greatest wavelength (320 nm). UV-B, however, also stimulates the dermis to form melanin by a complex series of reaction that stimulate melanocytes to trigger tyrosine in a multi-step reaction to form melanin. For this reason to occur, the skin must be stimulated by a dose of UV-B, close to the dose that causes redness. On excessive exposure to UV-B close to the dose that causes redness. On excessive exposure to UV-B (beyond one minal erythemal dose) (MED), the skin becomes pink after a delay of two to four hours Redness occurs, which, depending on the severity of the burn, will begin to fade from overnight to within three to four days. In severe case, the redness may result in separation of the stratum corneum by edema and 'blistering'. The wavelength of maximum redness within the UV-B range is near the peak of UV-B or 305 nm.
UV-A is not directly associated with erythema, and has a redness producing potential compared to UV-B of about 1/1000. However, it has been shown to damage the skin by penetration to connective tissue, and is also capable of producing tumours. In addition to damage by the deeper penetration of UV-A, photosensitizing or allergic response due to a causative chemical and UV appears to be primarily caused by UV-A. UV-A is able to produce melanin, but the tan is more unstable than the melanin created by UV-B exposure. UV-A is used in tanning salons because of its lack of erythema, and its relatively quick tanning. It is doubtful, however, whether tans produced by exposure to UV-A will provide resistance to significant amounts of UV-B. UV-A exposure in tanning salons is not without hazards, especially to the deeper underlying structure of the dermis.
Due to the damaging potential of UV-B. both near term (sunburn) and long term (skin damage), and the deeper penetration and potentially greater damage from UV-A. proper protection from UV-A and UV-B must be exercised. Exposures to both UV-A and UV-B have been implicated in increased number of skin cancers.
The amount of solar radiation varies depending on the season, the latitude, the time of day. and the altitude. The closer to the equator, the greater the total radiation from ultraviolet. The same is true for any location during the summer, when the sun is at its closest point. From 9 a.m. to 3 p.m. represents the period of greatest exposure, while increasingly higher altitudes add to exposure levels. In addition, when directly in the sun. there is from 10 to 100 times more UV-A exposure than UV-B exposure. Consequently, both bands contribute significantly to harmful effects. An additional concern is that the vast majority of UV emitted by the sun is absorbed by stratospheric ozone. There is recent evidence that this ozone layer is decreasing, which will allow more UV-B to penetrate. A decrease in the ozone layer ol 10% is estimated to increase melanoma by 10-20%. basal cell carcinoma by 25-35%, squamous cell carcinoma by 50-6094), and cataracts by 6-10%.
Sensitivity to UV irradiation depends on the amount of melanin, which absorbs UV, in the skin. Fitzpatrick and Pathak have developed a classification for skin types, depending on their response to UV irradiation (Table 2). This response is generally due to the level of melanin pigment in the skin. It is also typical of various racial or ethnic groups. Those groups who have a long history of sun exposure, e.g. black Africans, tend to be classification V or VI, while those with little history of sun exposure, e.g. people of Irish or Cellic heritage, tend to be category I or II. The normal reaction following exposure to meaningful amounts of UV is for the skin not only to produce more melanin, but also to thicken. The most serious effects are photodamage and cancer. Prolonged exposure can lead to profound changes in the fibrous component of (he dermis. with a decrease in collagen, alteration in keratinocytes and melanocytes and increased deep wrinkling and development of age spots. Continuous exposure leads to development on exposed areas of a wrinkled leather like appearance or 'red neck'. Skin cancers have been shown to be the direct result of overexposure to the sun. and the propensity of the individual to erythema and damage.
Australia, which has a high concentration of northern Europeans with Type I or Type II skin, and a location close to the equator giving maximized ultraviolet radiation exposure, has the highest reported incidence of skin cancer for a developed population. The most prominent form of skin cancer is basal cell carcinoma.
This cancer is typically preceded by a pre-cancerous lesion, a solar keratosis. This solar keratosis is easily removed by a dermatologist. The most serious form of skin cancer is a malignant melanoma, which usually arises from a mole and, it not treated early, is often fatal. Given the potential sun-damage to the skin, the need for sunscreen products is obvious. Some data suggest that 50% of a person's life time solar exposure occurs by the age of 18, therefore early usage is critical.
Sunscreen products are simply vehicles for materials (hat prevent meaningful amounts of UV radiation from reaching the skin. These materials are usually classified as chemical absorbers, or physical blockers and scatterers of UV radiation. In the US, they are recognized by the FDA 'over-the-counter drug regulations', which list various materials as Category I (safe and effective) sunscreens. In Europe, they form part of the EC and European Federation of the Perfume, Cosmetics and Toiletries Industry (COLIPA) positive list. An excellent review concerning the use of UV absorbers in sunscreen products has been written by Shaath. The materials can be grouped by name, chemical type, the wavelength at which they have maximum absorbance. al-lowed percentage usage in the US and EC, and by EC and COLIPA list numbers (Table 3). The vast majority of (he products listed in Table 3 are UV-B absorbers. The benzephones and butyl methoxy debenzoyl methane are UV-A absorbers. Titanium dioxide is a broad spectrum physical block.
Sunscreen products formulated with the sunscreen materials show in Table 3, at allowed or appropriate amounts, must be tested for performance. A number of in vitro performance tests have been developed and advocated, but the only currently accepted tests are in vivo tests. The standard tests vary from country to country, but are all similar. They are based on exposure to the sun or. more usually, to lamps that give carefully controlled amounts of radiation of very specific wave-lengths. A useful value has evolved to identify the efficacy of sunscreens. This is the sun protection factor or SPF, which is based; on production of redness on a test subject with a minima! erythemal dose (MED), representing the amount of exposure required to produce redness. The SPF is then the protection factor achieved with a specified layer of sun-screen applied to test subjects. For instance if individuals on average show a redness (MED) at 20 min. and. after the application of fixed amount of sunscreen product, show redness at 80 min. the product would have an SPF of 4. Much experimentation has been done to evolve alternative testing methods, and these are discussed in an excellent overall review of the subject of light protection by Groves.
The thickness of the applied film and lamps specified in sunscreen testing vary from country to country. The US and Europe differ significantly. Australia has separate standards and Japan is promulgating guidelines. Since these methods are under review and change, it is best to seek advice on acceptable testing from local trade associations, testing companies, sunscreen suppliers or regulatory bodies.
Another area of testing is that of waterproofness, which also varies from location to location. For instance, to support claims of waterproofness. the US PDA requires an in vivo test in which the subject is immersed in water for 80 min after application of product and then tested using the standard protocol. The claimed SPF must not be below the value achieved after immersion. Tests are now evolving and being advocated for testing protection versus UV-A exposure. At this point in time, no one test is yet accepted as standard.
Products that contain active sunscreens must be carefully formulated in order to ensure that the sunscreen material is in its active form, is available when used, does not contain materials that adversely shift or diminish its absorbance, meets the SPF claimed, is waterproof if required, and is cosmetically elegant. There are many forms available, including the common lotions (generally O/W emulsions), oils (solutions of sunscreens in mineral oil, vegetable oil. volatile silicones or esters), gels of a water or water/alcohol character, sprays, and sticks for special application. Many modern sunscreens are formulated with combinations of raw materials that have absorbance in both the UV-A and UV- B range, as well as physical blocks to augment protection.
The esthetic properties of products are also important, as the product must go on easily, spread uniformly and. if necessary, depending upon usage and claims, establish a waterproof film. In general, there has been a steady increase in SPF value, the spectrum absorbed and blocked, and the requirement for formulas to be waterproof. The US FDA has established regulations and, for instance, does not allow products to be marketed as sunblocks unless they have a proven SPF of not less than 15. It is now common for products to have SPFs greater than 15, with some having SPFs approaching 50. Products with high SPFs require considerable formulation skills to maximize the effect of sunscreens used, and to make an elegant and often waterproof product with actives that may be used at levels greater than 20%. Increasing levels of sunscreen can also lead to problems of product irritation.
Due to the variation in sunscreen formulations, and the multitude of active ingredients and product forms, a careful study of available literature and the marketplace is essential before meaningful exploratory work with formulation can be initiated. Although there are relatively few manufacturers of sunscreen chemicals, their help can be invaluable.
Suntan lotions These are generally O/W emulsions containing levels of UV absorber or physical blocks to give a desired SPF. Their formulation may differ from, that of conventional moisturizing lotions, in that significant amounts of oil phase are replaced by oil-based UV absorbers. In addition, if suntan lotions are required to be waterproof, they require addition of a water-repellent film former or some other means of ensuring adherence of the active to the skin. The following formula is that of a low SPF non-waterproof suntan lotion.
Procedure: Heat parts A and B separately to 70Â°C. Add part A to part B with good agitation. Mix to 35Â°C and add part C. Continue mixing until dispersion is complete.
Waterproof sunblock creams These formulas incorporate significantly higher levels of sunscreens, and also contain waterproofing agents. The following formula is for an SPF 15 waterproof O/W lotion.
Procedure: Add part C to part B and mix until uniform. Add ingredients of part A and mix to dissolve evenly. Hold at 85Â°C. To form the emulsion, add part A to the mixed parts of B and C at 85Â°C. Mix and cool to 35Â°C. Add part D.
Simian oils Suntan oils are typically used by individuals who are seeking a tan. rather than by individuals who are seeking protection. They usually have a low SPF and are used not only to afford some protection for a longer exposure, but also to give a glistening appearance to pigmented skins. They are seldom waterproof and incorporate oil-soluble sunscreens into mineral oil. vegetable oils and derivatives, fatty esters, and combinations of the above, at times with above, a times with volatile silicone added to decrease oiliness.
Procedure: Blend in order at room temperature. Ensure thorough dispersion of rarbomer before adding triethanolamine.
Sprays Most sprays are solutions of sunscreens in alcohol with or without, volatile silicone, or alcohol-soluble emollients. They can either be pump sprays or aerosol sprays, usually propelled by hydrocarbon propellanls. Such products are. by nature, light and easily spread on the skin. Since they are in volatile, bases, they tend to leave mainly sunscreen actives on the skin. Great care must be taken to ensure spreadability, and enough dispersion to ensure performance as well as maintenance of good estheties.
Procedure: Blend in order at room temperature. Ensure solution before addition of the next ingredient. Filter well before packaging.
Sun gels These products are often alcoholic/water solutions of alcohol-soluble sunscreens, thickened with gums or polymers. They are cool to apply and represent a small but loyal sub-segment of the category.
Procedure: Blend in order at room temperature. Ensure solution before addition of the next ingredient. Filter well before packaging Part A is 100% formula for the concentrate. Fill into an aerosol container and charge with a suitable propellant.
Sticks Sticks are usually for special application. They are of two general types: (i) for lips; and (ii) for areas that burn easily, such as the nose, ears and cheekbones. The formulas for lips are similar in nature to lip balm or lipstick formulas, and must be made of cosmetic raw materials that are edible. The products for areas that burn easily are often formulated with pigments that can act as total blocks. Zinc oxide, titanium dioxide, and talc are frequently used in a waxy matrix, not altogether different from the lipbalm products.
Procedure: Melt petrolatum and paraffin wax. Add other materials. Pour into molds or swivel sticks.
Procedure: Melt petrolatum and paraffin wax. Add other materials. Pour into molds or swivel sticks.
Everyday cosmetics with UV screens Many everyday cosmetic products, including colour cosmetics, are now being marketed with sunscreen actives in their formulation. Recently, protective UV variants of the most common hand and body moisturizer, as well as the most common facial moisturizer, were launched. These are products that contain sunscreens with an SPF of 4 and 15, respectively. It appears that many skin-care products for everyday usage will contain UV screens. It is critical for these products that the formulator takes extra care to ensure that esthetics do not suffer, that the active is stable, and that the products do not cause irritations with the mass of consumers who may be exposed to them on an everyday basis.
Acne vulgarises a disease that can range from occasional blemishes to a devastating, continuing episode leading to permanent scarring and much anguish. This section will discuss the various forms of acne and their treatment, except the treatment of cystic acne, which should only be treated professionally.
There are many misconceptions about aerie. It is not caused by diel. lack of cleansing, sleep or social habits, but by hormonal control. Both males and females secrete the male sex hormone testosterone. These secretions stimulate the sebaceous glands to secrete sebum. Acne is a disease that often develops due to genetic predisposition during puberty, and typically decreases during adulthood. The years of greatest severity are from 16 to 18 for women and from 8 to 19 for men. In white women, the incidence of clinical acne during the years of greatest severity is 40%, in men, the incidence is 35%. By the age of 40. 1% of men and 5% of women have lesions. The incidence among orientals and blacks is lower. The locations of acne lesions is generally on the face, neck, back and chest.
As discussed previously, the pilosebaceous system contains sebaceous glands and their associated hair follicles, both of which secrete sebum. Acne generally occurs in sebaceous glands that are either associated with fine or vellous hairs, or not associated with any hair. Humans are the only mammals that routinely develop acne; this is because they have lost their need for a hairy coating over the body, but still have many sebaceous glands without terminal hairs. In the presence of a coat, these glands would serve to wick sebum out on to the hair for the purpose of lubricating and waterproofing term
inal hairs, or for the purpose of providing an identifying odor.
As indicated previously, the sebaceous gland, with or without a hair, has its origin within the dermis. The follicle is, however, lined with statum corneum, creating the follicle wall. This stratum corneum sheds flattened dead cells into the follicle channel. This, combined with sebum, produces a mixture which, if it does not flow freely to the skin's surface, has the opportunity to plug, get infected and. through the enzymatic action of bacteria, break down certain components of sebum There are between 400 and 800 sebaceous glands per square centimeter, and it takes only one to become inflamed to cause an acne lesion. All of these are factors in the disease called acne, but none alone; is the direct, single cause. All individuals have sebaceous glands, containing sebum and bacteria. Some individuals have severe acne while others have little or no acne, sometimes only during adolescence. Individuals who develop severe acne are differentiated by the speed at which the epidermis lining the sebaceous gland produces and sheds cells. This is called retention hyperkeratosis. The increase of cells into an area rich with bacteria and lipid materials, including fatty acids, can cause an acne lesion. The acne lesion can be classified, and the acne graded by severity.
Closed comedones or whiteheads are impactions of cellular debris, sebum, etc., that buid up under the skin in the shape of an inverted 'U' with a nearly closed opening. The development of a comedone takes weeks and can lead to other stages, some of which are more serious. If the comedone matures without irritation, it becomes an open comedone or blackhead. The dark colour is due to the accumulation of dead cells and oxidized sebum, or collected melanin, not to dirt. If the comedone. with its rich supply of cellular debris, sebum and bacteria, becomes inflamed it is then a closed, red lump called a papule (commonly a pimple, a spot, or a zit). As the process of inflammation continues, the papule can build up white blood cells or pus. which arise from the body's attempt to fight the irritation. This is known as a pustule, or fluid filled pimple. If the inflammation continues, the follicle wall ruptures, and the inflammation spreads under epidermal surface and into the dermis, creating a nodule which is firm, red, but much larger and deeper than a pimple. In severe acne, several follicles become inflamed in an area and form a very large, merged, multiple pustule known as a cyst. Cystic acne is deep and can lead to much loss of tissue and scarring. The entire process, starting from an impacted sebaceous gland, and leading to cystic formation, can take-months from start to finish. In severe cystic acne, there is overlap of one episode to another.
Acne is identified by four severity grades.
Grade I is a mild acne, which has both open and closed comedones, or whiteheads and blackheads. This level is without redness, and dors not spread to adjacent tissue, or form pus. It is the first stage of the disease. Depending on the individual, it may develop in to more severe acne, remain at this stage because of treatment, or may actually recede because of treatment or the natural course of the disease.
Grade II consists of closed comedones or whiteheads that are present in a large number. They cause a bumpy surface and do not develop into open comedones or blackheads. This bumpy surface is generally without inflammation but, if left untreated, can lead to papules and pustules.
Grade III consists of both open and closed comedones, as well as comedones that have become inflamed and have progressed to papules and pustules. This grade of acne is severe, involves regions of redness, and can lead to light scarring.
Grade IV, or cystic acne, is most severe. Individuals in Grade IV not only have open and closed comedones, but papules and pustules that have merged together with much irritation, inflammation and eventual loss of tissue with scarring.
Acne of all but the most mild and transient forms should be treated professionally. Treatment can be either topical or systemic. Various treatments are available, either at retail or on a prescription from a physician, depending on their nature. Topical treatments sold at retail consist of benzoyl peroxide, salicylic acid, sulfur, resorcinol, and a combination of ethyl lactate and lactic acid. Topical preparations available on prescription are retinoic acid, and various antibiotic such as clindamycin and tetracycline. Oral therapy consists of antibiotic therapy with tetracycline or erythromycin and 13-cis-retinoic acid. The refinoids have revolutionized the treatment of severe acne. Topical retinoic acid decreases the cohesiveness of the pre-acne follicular epithelium, which leads to decreased microcomedo formation. In addition, it stimulates mitotic activity and causes extrusion of existing comedones. Systemic or oral administration of isotretinoin is used for severe or cyslic acne. It has been shown to affect sebum secretion, to have an inflammatory action, and to stimulate the immune system. Its primary function is to reduce overactive sebaceous glands to epithelial buds. It often results in a complete and prolonged remission of cystic acne. This oral therapy has severe side effects, including fetal abnormalities, extreme dry sin, and peeling, especially of the lips. Consequently, it must be carefully controlled and monitored, and is contra-indicated in female patients of child-bearing age, unless adequate steps to prevent pregnancy are taken. Treatment for Grades I, II or III acne is often a combination or oral and topical treatment. Isotretinoin is reserved for Grade IV acne that has been shown to be unresponsive to other treatments.
A wide variety of cleansing products are sold to acne-prone individuals. This include astringents, exfoliating scrubs, and buffing pads that are used to get the face very clean and to remove surface sebum. The products sold are satisfactory as cleansers, but do not provide adequate therapy for acne. This is because acne is caused by a combination of factors, all of which are operating in the sebaceous gland below the surface of the epidermis and, are not therefore, vulnerable to topical or surface cleansers, be they solvents (alcohol), exfoliants (polyethylene beads) or scrubbing pads of rough synthetic material.
As already stated, acne is a disease that can have devastating results on the appearance and psyche of individuals affected. In all but the most mild and transient cases, it is advisable to seek competent professional advice.
The use of liposomes in cosmetic products has increased during the 1980s and 1990s. The attractiveness of liposomes to both the cosmetic chemist and marketer comes from several factors. Liposomes are very small spheres consisting of a lipid bilayer. It is interesting to note that the skin's lipids are also organized into a similar bilayer structure. Liposomes range from 25-500 nm and vary with the lipids used and method of preparation. Liposomes are often formed with phospholipids, from lecithin of either vegetable (soyabean) or animal (egg yolk) source. However, liposomes can also be formed with non-ionic surfactant vesicles and other materials. Liposomes have been shown to be effective carriers for a wide variety of materials, both active and cosmetic.
Liposomes formed from phospholipids are notoriously unstable in finished formulations and may be stabilized by the addition of cholesterol to increase bilayer viscosity. The liposome may also be given a positive or negative charge by the addition of dicetyl phosphate or stearylamine. Liposomes have been shown to be capable of carrying drug materials within the sphere. Many drugs are made more, available to the body by (he use of liposomes (86). Ghyezy el al. have shown that even so-called empty liposomes formed from vegetable source phospholipids are able to increase the moisture content of the skin and improve roughness in comparison with a typical O/W emulsion.
Formulating with liposomes requires care in order to maintain the stability of (he liposome. Rules advanced by Brooks and McManus  are:
o Avoid surfactants or materials that can act as a co-solvent for the phospholipid
o Avoid materials with high ionic strength such as salts
o Avoid solvents such as alcohol that can remove the water that stabilizes the surface of the bilayer.
o Avoid excessive shear or temperature when adding the liposome to your final formula.
Procedure: Heat parts A and B separately to 75Â°C. Add part A to part B with good agitation and mix until uniform and creamy. Add part C and begin cooling with mixing. Add part E. then part D (liposome) and mix gently to 30Â°C.
Before referring to hair preparations information of general interest to the cosmetic chemist is discussed. This includes notes on hair growth, a survey of the biochemistry of hair, and other factors which are concerned with preparations for the care and treatment of hair.
Initially it is desirable to define hair as a modified epithelial structure formed as a result of the keratinization of germinative cells. A hair follicle is formed as a result of a down-growth from the epidermis into the dermis or subcutaneous tissue. At the depth of the down-growth a cluster of cells known, as the germinal matrix forms over a papilla of connective tissue which acts as a source of tissue fluids to the area. The part of the epidermis which has grown downwards becomes canalized between the germinal matrix and the surface and forms the external root sheath of the hair follicle. Proliferation of the cells of the germinal matrix forces the cells up the external root sheath and as they become further away from their source of nourishment, transition into keratin takes place. Growth of hairs is therefore the â€˜ result of continuous proliferation of epidermal cells of the matrix. In addition, these cells form a sheath of tissue known as the internal root sheath, which extends partly up the follicle, and separates the hair from the external root sheath. During the development of the follicle some of the cells forming the external root sheath grow out into the dermis and form sebaceous glands, with their ducts opening into the follicle. The hair follicles are usually in a slanting position and the sebaceous glands are generally on the obtuse angle of the follicles. The arrector pili is a small bundle of muscle fibres extending from the connective tissue sheath of the hair follicle on the obtuse side, upwards towards the dermis at a short distance from the opening of the hair follicle. Contraction of these muscles give the characteristic â€˜goose pimpleâ€TM appearance on the skin and at the same time promotes the flow of sebum into the hair follicle and onto the skin.
A single hair consists of the central medulla of soft keratin which is surrounded by the cortex of hard keratin. The outer surface consists of very thin flat overlapping scales which interlock to form the cuticle.
Figure 1. Diagram to illustrate structure of hair follicle in relation to Epidermis I. Corium II and Connective Tissue III showing Epiermis (a), sebaceous glland (b), arrector pili (c), medulla (d), internal root sheat (e), external root sheat (f), hair bulb (g), and papilla (h)
The medulla which always contains air spaces is present in what is known as coarse hair. There is no medulla present however in hair or blond types of hair. The colour of hair depends upon the amount of pigment present in the cortex. This pigment melanin is responsible for the colour of brown and black hair and other hair colours are also probably due to varying proportions of melanin type pigments. The melanin is formed in and by the epithelial cells of the matrix and the pigment is carried along by these cells as they are pushed up the follicle to become keratinized. If there is only a small amount of pigment present the hair appears white even though it may contain a dark medulla. Thus hair becomes white when melanin is no longer formed due to a change in the metabolism. Grey hair, therefore, is a mixture of white hairs and hairs containing varying amounts of pigment.
The process of keratinization of the epithelial cells which forms the hard keratin of the cortex and cuticle is similar to that which forms finger nails and the horny layers of epidermal tissue. Animal horn, feathers, and wool are similarly formed. The keratins consist of a large group of compounds which are obtained from keratinous structures, and in relation to hair they are often loosely referred to as â€˜hair keratin.â€TM Hair, however, contains at least the four keratins of the inner and outer cuticle, the cortex and the medulla. These vary slightly in composition and, for this reason, they are separately involved in the chemical reactions and physical behaviour of hair. The keratins belong to the group of fibrous proteins which includes fibrin, collagen, elastin and silk, protein and are composed of polypeptide chains. The building of a peptide chain is illustrated by reference to a basic amino acid structure thus:
Such a structure is joined to another amino acid by elimination of a molecule of water to give a di-peptide with the formation of a peptide linkage.
In similar fashion, a number of amino acids join together by peptide linkages to give a poly-peptide chain.
The polypeptide chains may take up different configurations depending upon the type of hydrogen bond which is formed between theâ€"CO and â€"NH groups. Hair keratins occur naturally in the alpha form, in which much of the hydrogen bonding takes place between the â€"CO and â€"NH groups of the same chain, as shown in the following diagram:
This diagram illustrates the chain-bundle formation of alpha keratin in the unstretched form described by Astbury.
If the hydrogen bonds are broken, the structure A to B can be stretched to give the beta form of keratin which is of similar configuration to that of silk fibrogen. The stretched form can be illustrated as follows:
This formation will, however, give a strained structure on account of the resistance due to cross linkages, in particular the disulphide linkages of the cystine residues present, and although hydrogen bonding has been broken between groups of the same polypeptide chain resistance will also occur due to the hydrogen bonding between neighbouring molecules of parallel chains. This stretched form therefore will contract to the stable alpha formation when the tension caused by stretching is released. The hydrogen bonding of the polypeptide structure A to B, with an adjacent chain, is shown below:
Permanent hair waving
There is evidence to suggest that a form of permanent hair waving was first practised by the Egyptians by tightly winding a mesh of hair on a cane stick, covering it with liquid mud and allowing it to bake dry in the sun. Wigmakers of old discovered that when hair was wound on a curling rod and immersed in boiling water, or steam for some hours, a permanent curl was obtained. They found that the time of immersion could be reduced considerably if a mild alkali such as borax was added to the water. The commercial possibilities of this process were first realized by Nessler in the early part of the twentieth century who claimed that hair can be stretched by 30 per cent when dry, 60 per cent when wet and up to 100 per cent when steamed, without rupture, In actual practice the safety margin is usually about two-thirds of these figures. Since stretched moist hair contracts to -its original length when it dries, to wave hair by this method it must be dried before contraction can take place. A waving process based on this principle consists of winding the hair onto wooden rods, and covering the mesh with a paste of borax spread on muslin. The treated mesh is then protected with a tube of brown paper and the whole cylinder enclosed by a heating iron. This is left on the head until all the moisture has been driven off and the brown paper is scorched. Opinions vary as to the most efficient alkali to use for this process and also as to its strength, and hairdressing specialists have their own fancies according to their experience. Two types of alkalis are employed; the non-volatile group containing borax, sodium and potassium carbonates and sodium bicarbonate, and the volatile group consisting of liquid ammonia and its salts. The main objections to the wave oils are usually an almost saturated solution of potassium carbonate.
During the 1914-18 war Eugene Suter developed a process for permanent waving based on the Nessler ideas. The hair is first saturated with a solution of an alkali, wound onto curlers and then wrapped in sachets. In this arrangement the heating element is close to the root of the hair and steam is generated inside the sachet. During this period several similar processes were developed, and in 1923 Sartory obtained patents covering the use of exothermic materials as a means of heating the hair. These methods are long and often painful but are, nevertheless the basis of the falling heat system still in use. A machine is used for the process. It consists of several metal bars mounted on a chandelier type stand, claims are attached to the bars which are electrically heated, the temperature being controlled by a thermostat. In the waving process the hair is first wetted with the wave solution and then wound onto curlers. The heated clamps are taken from the bars, placed over the curlers, and left for approximately ten minutes. The operating temperature is governed by the strength of the lotion being used and the tightness of curl required. The lotions are prepared with soluble sulphites or sulphides together with alkalis. Solutions of ammonium thioglycollate are also used with or without soluble sulphite. The success of the process depends entirely on controlling the amount of heat and the strength of solution. As a general rule a stronger solution of reducing substance requires less heat than a weak solution of reducing agent. Over heating in either case results in damage to the hair.
When the hair is wetted and wound on a curler, the strain produced causes the hair to form in the stretched and unstable beta-form. If the hair is left in this position and during the time the hair dries, it seems likely that some new linkages will be formed in the polypeptide structure which will be in line with the curled shape of the hair. When the curling pins are removed the hair will hold temporarily in its new stretched form. These curls are unstable and soon lose their new shape particularly if the hair is allowed to become damp.
Cold Waving Preparations
Cold waving preparations produce new permanent cross linkages in hair whilst it is held in the altered shape on the curlers, generally without applying heat. It can be said that the present methods of cold waving are based on work carried out on hair and wool by Goddard and Michailis, 1934 (J. Biol. Chem 106, 605), who showed that alka-without applying heat. It can be said that the present methods of cold waving are based on work carried out on hair and wool by Goddard and Michailis, 1934 (J. Biol. Chem 106, 605), who showed that alkaline solutions of thioglycollic acid reduce the disulphide linkages in the keratin of wool. From analysis of the amino residue of hair keratin it can be shown that hair contains about 17 per cent of cystine. The cystine molecule is made up of two amino acid groups linked together by two atoms of sulphur
These form cross linkages in the polypeptide structure as shown.
The content of cystine sulphur can readily be estimated and it is probably for this reason that the chemistry of waving has concentrated on the reduction processes which cause the breakage of the â€"Sâ€"S cross linkages of cystine. The general shape, elasticity and stability of the hair depends to a large extent on the cystine cross linkages since complete reduction of these structures results in breakdown of the fibre. The waving solution must break the disulphide linkages sufficiently to change their shape without destroying the fibres. An active reducing agent splits the cystine molecule into twt molecules of cysteine as illustrated:
and the second half of the process consists of reconstituting the cystine while the hair is still on the cullers by means of a suitable oxidizing agent.
This explanation is now considered to be a simplified version of the mechanisms which take place in the cold waving process. Reference has already been made to the hydrogen bonding which occurs in the polypeptide structure (see Fig. 5) and it would seem that these bonds must be involved in the waving process. This is confirmed by observing the effects of concentrated solutions of urea on hair. This substance, which is known to break hydrogen bonds, gives a tighter curl to hair when it is used together with a reducing agent. It is also possible to curl to hair when it is used together with a reducing agent. It is also possible to curl hair by using a solution of a hydrogen bond breaking substance only. Speakmanâ€TMs work (Speakman 1936, J. Soc. Dyers & Colourists 52, 335) on hair and wool shows that in addition to the changes involved in the breakdown of disulphide linkages the salt linkages across the peptide chains are also affected in the waving process.
Cold wave lotions for permanent waving are mainly based on thioglycollic acid, generally as ammonium thioglycollate. Mono-ethanolamine and isopropanolamine are also used as alkalis for neutralization of the acid. Lotions are prepared by ammonia neutralisation are considered to give a uniform curl and not have any adverse effect either on the appearance or control of the hair after processing. On the other hand, ammonia is constantly being lost by evaporation during the process and this is considered by some workers to contribute to a non-uniform result. Monoethanolamine thioglycollate gives a curl which is more difficult to control in the final set. Both monoethanolamine and isopropanolamine however, do not increase the odour level of the thioglycollate to the same extent as ammonia neutralized lotions. Sodium and potassium hydroxides gives thiogly-collates which are slower acting than the amine or ammonia neutralized preparations, and make the hair very soft to handle. For this reason they are only used occasionally lor neutralizing and then only ized preparations, and make the hair very soft to handle. For this reason they are only used occasionally for neutralizing and then only as a small proportion of the total alkali. It is claimed that a more uniform and natural curl can be obtained with monoethanolamine thioglycollate if a monoethanolamine salt such as the hydrochloride, sulphate or nitrate is included in the formulation together with a small proportion of a polyhydric alcohol (U.S. Patent 3039934). Thioglycollates are prepared by straightforward neutralization of thioglycollic acid with the selected alkali and final adjustment of the required pH value.
There are however, several precautions to be observed. Heat is evolved during the mixing process and both materials should be diluted before mixing, using iron free water for all the dilutions. The strength of concentrated solutions of ammonia should always be checked before dilution so that allowance can be made for any loss of strength which may have occurred during storage. It is also advisable to add ammonia solution below the surface of the acid to reduce losses of ammonia gas to the atmosphere.
All containers and mixing vessels should be made from, or lined with, glass or polythene, to avoid contact with iron and it is a good plan to provide loose covers for all vessels. Even contamination by particles of rust will cause the thioglycollate solution to become pink.
Lotions are prepared with varying concentrations of thioglycollic acid depending upon whether the final product is to be sold as a home-perm kit, or for professional use in the hairdressing salon. A general guide to the concentrations for particular requirements is as follows:
(1) Lotions based on from 5.0 to 6.0 per cent thioglycollic acid are suitable for easy-to-wave hair or for bleached and tinted hair. It is advisable to recommend a test application on a small mesh of hair in the latter case.
(2) Lotions based on 6.0 to 7.0 per cent thioglycollic acid are used for so-called normal hair. Concentrations of acid up to 8.0 or 8.5 per cent are used for hair which is generally described as difficult or hard-to-wave.
(3) For professional use lotions are prepared containing up to a maximum of 10 per cent thioglycollic acid. At concentration above this figure there is a risk of causing irritation of the scalp and permanent damage to the hair.
depends upon the pH value. For optimum waving effect this should be in the pH range of 9.5 to 9.7. If the pH value should fall to within a range of from 9.0 to 9.2 owing to loss of free ammonia during storage, the lotion will not give a satisfactory result even if the required concentration of thioglycollate is present. At pH values above 9.7 permanent damage of hair can occur by careless use of the lotion and there is also a possibility of depilation taking place. Control of pH value therefore, governs the effective performance of a waving lotion but does not necessarily control the degree of tightness of the curl. Soft or casual wave effects can be obtained with a lotion having a pH value below 9.5 but the wave is less â€˜permanentâ€TM than that obtained at the correct range of pH value. It is the method of winding the hair over the curlers and the number and size of the curlers used for the process which controls the appearance of the finished style. It is therefore most important to determine the pH value accurately by using a pH meter. The quantity of Tree ammonia present should also be estimated as a further check of the pH measurement. This is made by titration with deci-normal sulphuric acid, using methyl red as the indicator. From this determination a content of 1.40 grammes of free ammonia (NH3) per 100 ml of solution corresponds to a pH value of 9.5, and 2.20 grammes of free ammonia per 100 ml of solution is equivalent to a pH value of 9.7. Concentrations of free ammonia between these two limits are satisfactory.
To prepare a cold wave lotion therefore, the basic strength of thioglycollic acid must first be decided according to the type of hair or type of market for which the product is intended. The diluted acid is neutralized with the selected alkali by mixing in the manner described. Whichever alkali is used for neutralization the final adjustment of pH value should be made with ammonia solution.
There are several special additives which can be included in the formulation. Some of these are intended to maintain are stability and performance of the lotion in use whereas others are added to improve the appearance of the finished product. From 1.0 to 1.5 per cent of a surface active agent should be included as a wetting agent. For this purpose sodium lauryl sulphate or any other material normally used for shampoos can be used. Non-ionic surface-active agents are often preferred because these are more likely to be compatible with any other additives present. It is advisable to make practical use tests with all formulations to check the effect of the surface-active material. If too much is included the hair becomes slippery and difficult to with all formulations to check the effect of the surface-active material. If too much is included the hair becomes slippery and difficult to control during the winding process.
Polyvinyl pyrrolidone has also been suggested as a useful additive. The amount used should be from one to three per cent of the total volume of solution. It is considered that a proportion of the polymer penetrates the hair shaft during the process and gives the wave extra strength.
Clouding agent are often used to give an opaque or milky appearance to the finished product. This effect conforms with a popular notion implying that an opaque product has a gentle action on the hair. Clear lotions are also sold and manufacturers have suggested that this type of lotion also has special properties. Several materials are available for use as clouding agents, but before deciding which is the most suitable for a particular formulation, tests should be made for compatibility with other ingredients of the lotion and also to check that they do not settle on the bottom of the container during storage. Satisfactory clouding or opacifying effects can be obtained with a mixture of an ethylene oxide type of surface-active agent and cetyl alcohol. From 0.5 to 2.5 per cent of such a mixture is used according to the degree of opacity required. A similar proportion of a water soluble lanolin is also effective. Several speciality products are also available for use as clouding agents and details for using these can be obtained from the manufacturers.
A quaternary ammonium compound is sometimes included in the product as a conditioner provided this is compatible with the other ingredients of the composition. Suitable materials are:
(a) Cetyl trimethyl ammonium bromide.
(b) Stearyl dimethyl benzyl ammonium chloride.
(c) Dodecyl trimethyl ammonium bromide.
About 1.0 per cent gives wetting properties to the lotion and because these materials are substantive to hair give some softening effect. There is also less risk of the hair becoming frizzy and unmanageable on account of careless technique or over processing. The choice of suitable dyes tuffs is limited, and those offered by manufacturers should be carefully checked to ensure that they are stable during storage and not effected by the reducing action of thioglycollates.
Perfumes are also affected and must be tested for stability. The quality and purity of thioglycollic acid and thioglycollates manufactured during the last few years has improved considerably. As a re-consequently not so difficult to perfume. Perfumes stable to thioglycollates can be obtained from several perfumery houses. Those of a strong floral character such as sweet pea. violet, or wallflower are the most effective, and should be used at a fairly high concentration (up to 1 per cent) to provide effective cover. Perfumes based on flavouring materials such as raspberry are also used by some manufactures of professional lotions in an attempt to mask the prevailing odour of thioglycollates in the hairdressing salon.
Practical application of cold wave lotions generally follow a standard method of procedure but the results obtained can be varied according to the number and size of the curlers used. The hair is first shampooed, rinsed, and towel-dried. It is then divided into sections and wound onto curlers starting with the section at the nape of the neck. The lotion is applied to a mesh of hair with cotton wool or a sponge, combed though the length of the mesh and wound round a curler of the selected size. The hair should not be wound too tightly or fastened too near the scalp so as to cause tension at the hair root. Tight winding also prevents penetration of waving lotion and results in failure of process. Winding is continued at the back and sides, and finally the top front, large size curlers generally being used for this section. The wound hair is then redamped with lotion taking care not to allow an excessive amount to come into contact with the scalp.
About 10 to 30 minutes is allowed to complete the process but a guide to the length of processing time required can be obtained by examination of a test curl. A curler in the middle back section is carefully half unwound and the hair pushed towards the head. If a good wave moment is shown this indicates that the front section only requires about 5 to 10 minutes total processing. A poor waving movement of the test curl shows that a longer processing time is required and in this case a second test curl should be examined after a further 5 or 10 minutes processing time. When the hair has obtained the required amount of curl the lotion is thoroughly rinsed off with lukewarm water and the curlers blotted dry with a towel. The neutralizing lotion is then applied.
Lotions used by the professional hairdresser which are based on concentrations of up to 10 per cent of thioglycollic acid are prepared by neutralizing the acid either with monoethanolamine or by neutralizing the acid either with monoethanolamine or isopropanolamine and the pH adjustment made with ammonia solution. With these stronger solutions a different technique can be used for the method of application. After the hair has been shampooed, rinsed, and towel dried the wave lotion is applied with a sponge or cotton wool and distributed evenly throughout the hair by combing. The hair is divided into sections and wound on to the curlers as already described, each mesh of hair being re-wetted with lotion before winding. Hot water is then sprayed over each curler whilst the head is held over the wash basin, the water being as hot as possible without causing discomfort. Spraying is continued until all the lotion is completely removed from the hair. The curlers are dried with a towel and a neutralizing solution applied in the usual manner. The procedures of applying thioglycollate solutions and the removal of the lotion by rinsing complete the first half of the waving process. At this stage the hair is in a softened and swollen condition, and in its new shape.
The second half of the process consists of neutralizing the reducing agent to reconstitute or stabilize the hair keratins in their new shape. This is also referred to as the hardening process. Neutralization therefore can be carried out by a procedure which involves oxidation. If the hair is unwound before oxidation has taken place, it will not take up the new shape. The hair will, in fact be straight, and this principle forms the basis of preparations used for straightening curly hair.
Neutralizers consist of mild chemical oxidizing agents such as sodium perborate, sodium or potassium bromate or sodium percarbonate. When supplied as part of a home-perm outfit they are packed sealed in separate sachets and the powder is dissolved in lukewarm water immediately before use. This is poured over the curlers for several minutes in order to saturate the hair thoroughly. After application it is advisable to leave the neutralizing lotion on the hair for ten or fifteen minutes. This allows time for oxidation to take place and the success of the whole process depends upon complete and effective oxidation. The hair is then rinsed with lukewarm water, and the curlers removed. Finally the hair is given a further rinsing with lukewarm water.
Neutralizers for sale in powder form are simply made by preparing sealed envelope type packages each containing about 5.0 grammes of the oxidizing chemical. Potassium bromate is the material often used since it has a mild action and does not have any tendency to cause when the oxidizing agent is applied. To counteract alkalinity of the waving lotion, a buffer salt with an acid reaction in solution can be mixed with the oxidizing agent. Sodium dihydrogen Phosphate (NaH2 PO4 H2O) is used as a buffering agent in the following formula:
10 grammes of the mixture is used for each package of neutralizer.
These two chemicals react together if moisture is present and they also tend to cake. To prevent this they should be dried separately before mixing until the moisture content is about 0.01 per cent. After mixing pack in sealed moisture-proof containers. Neutralizers are also prepared as creams or lotions which do not require a preliminary mixing procedure. They are supplied as part of a home-perm kit and are also used by professional hairdressers. A typical formula for a lotion or thin pourable cream is prepared as follows:
Procedure: Warm A until homogenous and B in a separate container until the bromate has dissolved. Add B to A with stirring. Add any perfume and continue stirring until the mix is cold.
A neutralizer of a firm cream consistency with an attractive pearly sheen suitable for home or professional use can be prepared to the following formula:
Procedure: Dissolve the S.D.M.B.A.C. and sodium bromate in water by warming gently to 70Â°C with constant stirring. (Stirring is essential to prevent the bromate settling.) In a separate vessel melt together the cetyl alcohol and emulsifier at a temperature of 70Â°C and add the bromate solution with continuous gentle stirring. Mix and allow to cool and add the perfume.
Hydrogen peroxide solution is an effective neutralizer and a dilute solution is often used by hairdressers as a final rise after the application of a more conventional preparation.
Foam neutralizers can be prepared by mixing hydrogen peroxide solution with an emulsion or detergent base immediately before thev are required for use. An emulsion base is prepared from a mixture of waxes such as cetyl alcohol or stearic acid together with a suitable surface-active material. Use of a surface-active agent is indicated as follows:
2. Solution of hydrogen peroxide (acid stabilizer) 20 volume
Procedure: Dissolve the sodium chloride in part of the water. Mix the sodium lauryl ether sulphate with the remaining water and add the sodium chloride solution.
When required for use one part of the â€˜foam neutralizerâ€TM is added to an equal amount of hydrogen peroxide solution, and mixed vigorously until a light foam-like preparation is obtained. Foam neutralizers are effective because they contain a high proportion of surface-active material which helps to penetrate the hair wound on the curlers. They are also easy (o control during use. Foam type neutralizers are also prepared by mixing a solution of sodium bromate (10 per cent) with a suitable liquid or paste type shampoo base.
Procedure: Dissolve the sodium bromate in the water without the aid of heat and mix with the shampoo base.
A comparatively new idea in the technique and application of cold waving preparations is to combine the waving process with a hair colourant. This is carried out by incorporating an acid or basic dye-stuff in the neutralizer. Any of the formulae for liquid or cream type neutralizers can be used although formula No. 2104 which contains a quaternary ammonium compound is particularly recommended.
Cold wave lotions are also sold without a neutralizer in which case the directions for use are modified. After the thioglycollate lotion has been removed by rinsing, the curlers are left on the hair for four to six hours or overnight until it is dry. Neutralization in this case is by slow and gradual air oxidization. More permanent results are generally obtained when a chemical oxidation process is used.
Hair straighteners are also related to cold waving preparations and are a thioglycollate treatment â€˜in reverse.â€TM They are used to straighten kinky or negroid type hair but in this case the reduction process breaks down the â€"Sâ€"S linkages of the curly hair and permits them to reform in the uncurled shape. The curlers are removed after thioglycollate treatment when the hair is in a softened condition be- fore application of a neutralizer. After rinsing, a firm cream similar to that given under Formula No. 2104 is applied since this helps to set the hair firmly in its new shape in addition to its neutralizing action.
Shampoos continue to have a tremendous sale and the development of synthetic detergents most probably accounts for the growth of this market. The modern shampoo is designed to provide sufficient cleansing power together with adequate foam, to remove soil from the hair and scalp without seriously reducing natural oilinessâ€"so that the hair is left with a natural gloss and in a soft and manageable condition.
The function of a shampoo has been variously defined by several workers. The author considers that an acceptable shampoo should have the following characteristics:
1. It should remove the build- up on the hair and scalp of surface soil, excessive sebum, and residues of setting lotions and dressings.
2. The degree of foam should be sufficient to satisfy the psychological requirements of the user.
3. The shampoo should be removed easily by rinsing, and leave the hair in soft and lustrous conditions, with good manageability and a minimum of fly-away.
4. The shampoo should impart a pleasant fragrance to the hair during use, in order to mask the odour of wet hair. It is, however, not essential for the perfume to be substantive.
It should be noted that the cleansing properties defined above give an indication of the required degree of detergency, since over degreasing leaves the hair dry, frizzy and unmanageable. New synthetic detergents are constantly being offered as suitable bases for shampoos but it is probably true to say that the majority of shampoos on the market are based on sulphated fatty alcoholsâ€"known commercially as lauryl or alkyl sulphates. These may include monohydric alcohols of chain length C10 to C18. It is generally understood that a high degree of sulphalion is necessary to obtain good detergency, and this is often used as the criterion when good solubility and low cloud point are required. On the other hand, a certain amount of foam is desirable and foam stability is achieved to some extent by the presence of some unsulphated alcohol. Development of foam, however, does not always indicate good detergency.
The properties of these detergents depends upon the chain lengths of the fatty alcohol used. Thus an alkyl sulphate based on C12 (lauric) and C14 (myristic) alcohols gives a wet and billowy type of lather with good cleansing properties at lower temperatures than those based on C10 (palmitic) and C18 (stearic) alcohols. Since the solubility of the sulphated alcohol decreases as the chain length of the fatty alcohol increases, shampoos based on C16. and C18 alcohols, have poor cold storage properties. Because of this they are less soluble in water and they give less foam at normal shampoo temperatures. The hardness of water has also more effect on alcohol sulphates of higher molecular weight. Another factor to consider is that C8 (caprylic) and C10 (capric) alcohol sulphates tend to be irritant, and it is useful for fractions to be carefully cut to eliminate all the C8 alcohols and nearly all the C10 alcohos. Alkyl sulphate based on C12 and C14 alcohols are non-irritants, have good storage properties, and give the most acceptable type of lather at normal shampoo temperatures.
The properties of a sulphated fatty alcohol are also influenced by the cation present. Thus, sodium alkyl sulphate has more degreasing action than the ammonium or triethanolamine compound, and because of its harsh cleansing action sodium alkyl sulphate is now generally only used as the base of compositions for the treatment of greasy hair. This treatment can nevertheless be criticized, since complete degreasing can promote an increase in the flow of sebum. In addition after a degreasing treatment the hair is dry, frizzy and unmanageable and has a dull appearance. The modern conception of a successful shampoo accentuates the manageability of the hair immediately after shampooing and in this context the most popular detergents are triethanolamine or monoethanolamine compounds, which have a mild cleansing effect. Triethanolamine alkyl sulphate which is probably the most widely accepted cleansing agent used in shampoos has the added advantage of good storage stability. Ammonium alkyl sulphate which also has a mild cleansing effect, is seldom used alone because of its high solidifying point. It is usually used blended compounds such as ammonium-monoethanolamine, and ammonium-triethanolamine alkyl sulphates. Shampoos formulated with these bases have good foaming and cleansing properties but still leave the hair manageable.
In addition to the sulphated fatty alcohols, shampoos with particular characteristics can be prepared from sulphated fatty ethers. The sodium salts of sulphated lauryl alcohol ether are available as colourless liquids of different viscositiesâ€"and give profuse and stable foam. The viscosity of the diluted product can also be easily adjusted and controlled by the addition of a predetermined amount of sodium chloride or any other suitable electrolyte.
The search for the perfect shampoo has also led to investigation of the the effect of additive materials to the basic detergent. Fatty acid alkylolamides are used to increase stability of the lather and control the viscosity. These are condensation products of fatty acids with either mono-or diethanolamine or the corresponding isopropanolamine. These materials also disperse insoluble line and magnesium soaps produced during washing and prevent their deposition on hair and scalp.
The correct choice of detergent base plus additive, which governs the performance characteristics of a shampoo is closely correlated to the manageability and final appearance of the hair. To this end many additives claimed to have conditioning properties have been suggested. These include lanolin or one of the lanolin derivatives, cholesterol, oleyl alcohol and acetoglycerides. Additives such as lanolin or egg powder are frequently used and special claims are made that these materials will give the hair lustre and manageability. Although it is questionable whether such materials can have any influence on the final condition of the hair, they may assist by reducing the degree of degreasing, and in a two-application shampoo some deposition on the hair fibres may increases gloss or lustre. Materials of this type, however, invariably reduce the amount and stability of the foam if they are added to standard compositions.
An interesting observation based on chemical investigation claims that if amino acids are added to a shampoo, some deposition remains on the hair and scalp after shampooing. It is considered that there is a hygroscopic substance present in hair which is required to maintain the hair in good condition. This hygroscopic material mainly consists of amino acids. Thus, if amino acids do remain on the hair and scalp after shampooing it is possible that the hair will benefit by including a suitable hydrolysate containing all the essential amino acids. Formulations with this type of additive form the basis of protein shampoos.
Other additives examined for their effect on foam formation and stabilization include the glycols and polyvinyl pyrrolidone. Carboxymethyl-cellulose has been used with detergents as a soil suspending agent; and it has also been found that liquid silicones, particularly at a concentration of about 4 per cent, increase foam stability, improve setting properties, and give gloss to the hair.
Evaluation of Shampoos
In the formulation of shampoos, the physical properties must be related to the performance characteristics, and several laboratory techniques have been developed for this purpose. Some success in the measurement of foams has been achieved by using simple stirring devices in graduated temperature controlled vessels and the effects of adding selected oil such as lanolin, mineral oil or vegetable oil can be determined. Ross and Miles (Miles, G.D. Ross. J. and Shedlovsky, L.J. Am. Oil Chemists Soc. 27, 26-273) developed a satisfactory method for evaluation of foam, and although this method does not gives results which can be correlated to practical application, is useful for screening purposes. Myddleton designed an apparatus for the measurement of foam quality which could be related to the results of foam quality which could be related to the results of actual shampoo tests made with the same source of detergent (The Evaluation of a Shampoo. Myddleton, W.W., J. Soc. cos. Chem. Vol. IV, 150-156).
The final assessment of a shampoo, or an individual detergent, however, is probably best determined by practical demonstration. For this purpose, the half-head techniqueâ€"practised according to a standardized procedureâ€" is often employed. This can be used to provide instructions which will be issued with the finished product. The data obtained should include the amount used, details of dilution, the number of applications, information on temperature, time of lather formation, volume and texture of lather, and ease of rinsing. The following is the normal procedure:
(a) During the application of a test shampoo or detergent it is advisable to note the texture and volume of the lather, together with its degree of stability and odour.
(b) The condition of the wet hair should be examined after rinsing for information on feel and effect of combing. Information regarding the odour value of a perfume can also be obtained at this stage.
(c) A similar examination should be made after the hair has been towel-dried. Needless to say, for the purpose of these tests, setting lotions should not be used.
After some experience of the half-head technique, minor variations in the performance of a shampoo or detergent can be identified and small differences in the final condition of the hair noted. The important data finally obtained includes: the degree of gloss or shine, development of highlights; ease of combing; assessment of fly-away; and degree of manageability. A similar standardized technique also can be used for evaluating perfumes in standard shampoo compositions.
Shampoo formulations can be classified into the following main groups:
The earliest types of shampoo powders were prepared by the simple admixture of diluent or extender with soap powder. Sodium carbonate, bicarbonate, sodium sesquicarbonate, disodium phosphate or borax are suitable diluents.
Shampoos of this type continue to be of some interest. They can be used with henna or chamomile to give products which are supposed to give a slight colouring effect to the hair. A henna shampoo can be prepared as follows:
The following formula can be used to prepare a camomile shampoo:
Partly because of their poor performance in hard water, powder shampoos based on soap have now been superseded by synthetic detergents. Sodium lauryl sulphate is generally used as the base lor these products. This material ean be obtained from the manufacturer as a white, free flowing spray dried powder in various concentrations. About 5 grammes of the pure compound is required to give a satisfactory shampoo and to increase the bulk it is mixed with a suitable diluent. Manufacturers also supply the alkyl sulphate in diluted form (perfumed if required) ready for packaging. These are prepared by spray drying the alkyl sulphate generally with sodium sulphate as the diluent.
Dry shampoos are sold in powder from although these products have a limited sale. They are useful for use between wet shampooings or when it is inconvenient to use water and are particularly effective when the hair is greasy. Provided all the powder is removed by brushing they give a quick method of improving the appearance of lank or drooping hair. They are made from powders with absorbent properties such as tale, kieselguhr or starch.
Liquid Dry Shampoos
Liquid dry shampoos are also used as a method of cleaning the hair and scalp when time is not available for the usual lather type shampoo. They are mainly designed to remove grease by use of suitable solvents such as alcohol, and when applied with gentle message of the scalp they have a pleasant refreshing effect. They can also be used as a means of leaving the hair pleasantly perfumed. This type of product is also sold as a lacquer removing shampoo but since there is no actual washing or rinsing procedure in the treatment any lacquer on the hair must be dissolved rather than removed. On the other hand if hair and scalp is massaged with a lotion which contains a high proportion of alcohol and a suitable plasticizer, some of the lacquer on the hair will be softened or dissolved and removed during towel drying. The effects are likely to be most noticeable when a rigid film forming type of lacquer has been used on the hair. A suitable product can be made using the following:
Clear Liquid Shampoos
Clear liquid shampoos have already been referred to in the general discussion dealing with behaviour characteristics of detergents. The detergent and additive used in formulating are selected to give the required performance. The viscosity of the product and correct choice of auxiliary additives such as perfume and colour are also important factors to consider. The basic detergents are available from the manufacturers as solutions which differ either in physical characteristics including viscosity or in content of active material. So called built detergents are available which are preformulated and contain an alkylolamide.
There is a general method of manufacture which can be followed for all clear liquid shampoos. If an alkylolamide is being used this should first be dissolved by heating gently with about half the total amount of detergent until solution is effected. The remaining quantity of detergent is then added gradually. The perfume is dissolved in the cold concentrated detergent. Any colour is dissolved in an adequate amount of water and added to the mix. The remaining water is finally added with gentle stirring to avoid incorporating air bubbles and the formation of an excessive amount of forth.
A preservative should be included in all the formula which are given and 0.2 per cent of solution of formaldehyde (40 per cent) is recommended. Phenyl mercuric salts are also effective, at a concentration of 0.001-0.002 percent but as these are poisonous their use should comply with Poisons regulations. Phenyl mercuric borate is preferred because it is more soluble in water.
Perfumes are used in shampoos at concentrations of from 0.3 to 1.0 per centâ€"0.5 per cent being a generally accepted level. It is also usual to add a suitable proportion of a water soluble dyestuff.
The formulae which follow have been selected to give shampoos with the characteristics and acceptable performance already described.
1. Empicol TL 40 type-Albright & Wilson Ltd.
2. Empilan LIS type-Albright & Wilson Ltd.
2. Empicol TLP type-Albright & Wilson Ltd., Marchon Division.
1. Empicol TLP type-Albright & Wilson Ltd., Marchon Division.
1. Empicol LQ 27 typeâ€"Albright & Wilson Ltd., Marchon Division. Cycloral SA typeâ€"Cyclo Chemicals Ltd.
2. Empilan LIS typeâ€"Albright & Wilson Ltd., Marchon Division.
Several variations of this formula can be made by increasing the amount of alkylolamide and decreasing the detergent without affecting the viscosity of the product to any marked degree.
1. Cycloryl SA/N type-Cyclo Chemicals Ltd.
Optical brighteners (optical bleaches) are useful additives particularly for use with clear liquid shampoos although they can also be used in creams and lotions. These materials increase visible light reflection and are considered to give the hair more lustre. Fluorescent materials are also used for the same purpose. A Swiss* patent describes a similar effect by using a colourless hair-substantive organic coumarin derivative.
Concentrated clear liquid shampoos are prepared for sale either to manufacturers who simply dilute the concentrate with water before packing in bottles for retail distribution or to hairdressers who dilute the product as required for use in the salon. They are particularly useful for hairdressing premises since they help to solve the problem of storage of large amounts of liquid. Concentrated clear liquid shampoos can be made as follows:
properties, and is suitable for use as the active ingredient in medicated shampoos. It is insoluble in water but solution can be effected by dissolving the compound in a small quantity of alcohol or alkali before adding to the shampoo base. The compound which is substantive to skin and hair is effective at a concentration of 1.0 to 1.5 per cent. Small amounts retained on the scalp after shampooing reduce resident bacteria by 97.5 per cent. The compound is also used as the active material of antiseptic or deodorant soaps.
2,4,4' -trichloro-2'-hydroxydiphenyl ether (Irgasan DP 300â€"Geigy) is a white powder with a faintly aromatic odour, and is an effective bacteriostat active against bacteria and certain fungi. It is insoluble in water but solutions can be prepared by dissolving the compound in a small quantity of alcohol, or the surface active base, before mixing with the remaining ingredients of a shampoo.
Hexachlorophane (Di 3: 5:6-trichloro-2-hydroxyphenyl methane) is an effective bactericide which retains its activity in the presence of soap and detergents, and daily use of soap containing hexachlorophane reduces the bacterial flora of the skin. It has been used successfully in shampoos at a concentration of 0.5 to 2.0 per cent. Recent experimental studies in the United States have indicated that in certain circumstances hexachlorophane can induce brain damage in animals. It is suggested that a potential health hazard may exist, particularly to infants, when total body bathing or widespread application of a product containing hexachlorophane is carried out without subsequent rinsing.
The Committee on Safety of Medicines have recommended that products containing hexachlorophane for medicinal use on infants, such as talcs, powders, creams, lotions, and emulsions, should only be recommended on medical advice. There is, however, no evidence to date that preparations containing hexachlorophane are harmful to human adults, and attendant risks would appear to be minimal in a shampoo, when adequate rinsing forms part of the normal shampooing procedure.
Prepared coal tar, B.P. (Pix Carbonis Praeparata), is a well known antiseptic used for the treatment of pruritus, psoriasis, and eczema and is used to alleviate itching. The most convenient way of using coal tar is in the form of coal tar solution (liquor picis carbonis B.P.)â€"a solution prepared by macerating 20 per cent of prepared coal tar and 10 per cent quillaia in alcohol. The quillaia forms a milky dispersion of coal tar when it is added to water, but is readily soluble in surface-active materials. Clear alcoholic solutions can be prepared by macerating prepared coal tar in alcohol only and quillaia, filtering out insolubles after maceration.
Medicated shampoos are prepared containing either one or more of the antiseptic materials given and several heterogeneous compositions have appeared on the market.
Typical mixtures of active ingredients for use with the shampoo bases already mentioned are as follows:
In the above formula, oil of rosemary and methyl salicylate are included for their odour value only. In similar fashion suitable proportions of dispentine or oil of pine can be included.
The following are also used as active ingredients of medicated shampoos:
Resorcinol (m-dihydroxybenzene) occurs as a colourless powder and is a useful material to relieve itching. In shampoos it is usually used at a concentration of from 0.05 to 0.10 per cent. When the powder is exposed to light and air or used as an ingredient of alcoholic solutions it becomes pinkish in colour. An alcoholic solution of resorcinol also has a tendency to discolour fair hair slightly. It is not likely to give any trouble at the concentrations normally used in shampoos.
Oil of eucalyptus is used in medicated shampoos, generally at a concentration of from 1.0 to 2.5 percent. It has a characteristic aromatic eamphoraceous odour and when applied externally has a cooling effect and counter- irritant properties. Eucalyptol or Cineole is one of the main constituents of eucalyptus oil and has similar properties to oil of eucalyptus. Use from 0.25 to 0.5 per cent in medicated shampoos.
Cade oil also known as juniper tar oil or juniper tar is a dark reddish brown oily liquid with a tarry odour. It is sometimes used (at about 0.25 to 1.0 per cent) to stimulate circulation.
Ichthammol or ammonium ichthosulphonate obtained by distillation from certain bituminous shales occurs as a black viscous liquid with a strong characteristic odour. It is slightly bacteriostatic and reduces inflammation. Use from 0.5 to 2.0 per cent. Although both cade oil and ichthammol effect the colour of a product they are nevertheless materials which are useful to prepare a speciality treatment preparation.
Precipitated sulphur is used externally as a mild antiseptic and parasiticide. It is usually applied in lotion or ointment form in order to maintain intimate contact with the skin. Salicylic acid is a bacteriostatic and fungicide also used in lotions and ointments for treatment of the scalp. Up to 2.0 per cent of these two materials can be used in medicated shampoos preferably in a cream or paste type base. A micropulverized sulphur is recommended.
Cationic surfactants are so termed because the surface active portion of the molecule is contained in the positively charged cation. On this account they are substantive to hair and skin and have antistatic properties. Unlike the anionic surfactants many cationic compounds have achieved commercial importance in applications where surface activity as such is a minor consideration. Thus where the cation is present as a quaternary ammonium group attached to a long chain alkyl group, the compounds can be used as detergents or emulsifying agents and also for their bactericidal properties. As bacteri-cides their properties vary according to the chain length of the alkyl group. Compounds of high molecular weight have lower bactericidal properties. Care must be exercised in selecting a particular quaternary ammonium compound when this is to be used for regular application to the hair and scalp since a material with high bacteriostatic properties may cause defatting of the skin and give rise to irritation. Several cationic surfactants are used to prepare medicated shampoos, as a specific treatment for dandruff and associated irritation of the scalp. The following are particularly recommended:
Cetrimide B.P. (CTAB) consists of a mixture of dodecyltetradecylâ€"and hexadecyl-trimethylammonium bromides. It is non-irritant and non-toxic in the dilutions generally used.
Benzalkonium chloride is a mixture of alkyl dimethyl benzyl ammonium chlorides, and has similar bactericidal and bacteriostatic properties to cetrimide. At high concentrations of the order of 12 per cent it is slightly less toxic than cetrimide.
Stearyl dimethyl benzyl ammonium chloride is another typical quaternaiy ammonium salt and although this material has less bactericidal action then either cetrimide or benzalkonium chloride its use also improves the appearance of the hair.
Medicated shampoos based on quaternary ammonium compounds are prepared as follows:
Procedure: Dissolve the cetrimide in water using gentle heat. Cool to 35ÂºC and add the mixture of diethyl pththalate and alcohol. Add perfume and stir gently until homogeneous.
Cetrimide B.P. is soluble in two parts of water but to maintain clarity of solution during storage a small proportion of alcohol is included in the above formula. Diethyl pththalate increase the viscosity of the shampoo. Other quaternary ammonium compounds such as hexadecyl trimethyl ammonium bromide can be used in the above formula if required in place of cetrimide. For this type of product use a concentration of 15 to 20 per cent active material. Any perfumes used in these mixtures should be carefully checked for stability.
A cream shampoo for treatment and control of seborrhoea capitis and seborrhoeic dermatitis can be prepared as follows:
1. Cetrimide B.P. or hexadecyl trimethyl ammonium bromide
Procedure: Warm gently the cetyl alcohol and alkyl trimethyl ammonium bromide with 200 parts of water. Stir gently until homogeneous and add the remaining water at about 40ÂºC. Add perfume and colour and mix.
For use, the hair is first thoroughly wetted with warm water and about a teaspoonful of cream or lotion is massaged well into the scalp with the fingers. An extensive lather is not obtained. The hair is then rinsed thoroughly and the application repeated and on this occasion the shampoo can be worked up to produce a lather. Finally the hair is thoroughly rinsed with warm water. Care should be taken to keep the preparation away from the eyes. It is claimed that weekly treatment controls seborrhoeic conditions and maintains the scalp and hair in a healthy condition.
A liquid cream shampoo with an attractive pearly sheen can be prepared to the following formula:
1. Empicol LQ 27 typeâ€"Albright & Wilson Ltd., Marchon Division.
Selenium sulphide SeS2 is a bright orange powder which was developed by Norlander (U.S. Patent Nos. 1711742, 1860336). It is used in the form of an emulsion or with a surface-active agent in persistent cases of seborrhoea capitis. Sometimes during the treatment, the hair becomes oily and occasionally hair loss occurs. Hair loss of this nature very often takes place after shampooing a seborrhoeic condition and is generally only of a temporary nature. It has been reported however, that use of selenium sulphide appears to bring about changes in the hair roots which results in weakening of the hair. When persistent hair loss occurs, treatment with selenium should be stopped.
Selenium sulphide preparations are generally described as creams or suspensions and are considered primarily as a medicated treatment rather than a shampoo. Formulation with selenium is difficult on account of its insolubility and it is more easily handled if mixed with a suitable inert diluent before adding to a surface active agent. Norlander found that by heating equal parts of selium disulphide and bentonite to a temperature where fusion of the selenium occurred, the resultant mixture could be easily dispersed in water. This mixture was shown to consist of selenium monosulphide SeS. A typical selenium preparation for treatment and control of seborrhoea capitis can be prepared as follows:
Mix the selenium disulphide and bentonite until the selenium is evenly dispersed. Heat the sodium lauryl sulphate and water in a steam jacketed vessel fitted with a stirrer. Stir gently to a temperature of 90ÂºC. In a separate vessel add a suitable proportion of the detergent mix to the selenium dispersion and stir until homogeneous. Add to the main mix and continue stirring. Cool to 40 to 45Â°C and fill.
A firmer cream can be prepared by adding 0.5 to 1.5 per cent of cetyl alcohol to the formula. This helps to disperse the selenium if added during the preparation of the concentrated selenium detergent mix.
Selenium preparations are generally applied twice a week for the first two weeks of the treatment and once a week for a further two weeks. After this they are used occasionally between the use of ordinary shampoos to maintain control of the seborrhoric condition. During application continuous massage of the scalp is desirable and after treatment thorough rinsing should be carried out to remove all traces -of the preparation.
Undecanoic acid or undecylenic acid is a fungicide used for the treatment of athleteâ€TMs foot and other superficial fungal infections of a dermatological nature. It is usually used in conjunction with zinc undecanoate either as ointments, emulsions or dusting powders, the total concentration of active fungicide being about 10 to 15 per cent. Undecanoic alkanolamides derived from unclecanoic acid and similar aliphatic acids of medium chain length are fungicidal and bactericidal compounds suitable for treatment of seborrhoea capitis. These materials which are non-allergenic and non-sensitizing are substantive to keratin and on this account are useful materials for use in shampoos, since some retention of antiseptic properties occurs on the hair and scalp alter shampooing. They have a characteristic musk-like odour and although this is less pronounced than the odour of undecanoic acid this factor must be considered when selecting a perfume. Floral perfumes of a rose or violet type generally blend satisfactorily.
Several compounds are available commercially. Those derived from mono-alkanolamides of fatty acids of medium and short chain lengths are waxy solids with varying melting points (Loramine U. 185, 1PU. 185). They are almost insoluble in water, but soluble in alcohol, aqueous-alcoholic mixtures, organic solvents, and oils and fats. Shampoos can be formulated by first dissolving the compounds in alcohol or the perfume oil and mixing with a suitable detergent base such as triethanolamine lauryl sulphate. The surface-active material of the shampoo base increases the activity promoting intimate contact of the compounds with fungi and bacteria. The compound derived from undecanoic acid and diethanolamine is available commercially in the form of a loose complex containing a percentage of amine soap (Loramine DU. 185). On this account it has a greater solubility in water than the waxy materials. Aqueous solutions containing 2 per cent of the compound have sufficient wetting and foaming properties to be used as detergents on their own but a more satisfactory product is obtained by using a base of triethanolamine lauryl sulphate. Undecanoic mono-alkalolamide has also been prepared as a sodium sulpho succinate derivative (Loramine SB. U185). This compound is available as a cream coloured paste with a weak but characteristic odour containing 50 per cent active matter. It has been shown to be an efficient, non-toxic fungicide and baeteriostatic and is substantive to keratin.
In water the compound gives a slightly opalescent solution but it is readily soluble in luke-warm water. Clear solutions can be prepared by mixing with surface-active agents or by dissolving in a mixture of alcohol and water using 30 to 60 per cent of alcohol. Optimum solubility can be obtained by using aqueous iso-Propyl alcohol. The compound can thus be used for the treatment of seborrhoea capitis as a medicated shampoo or a scalp lotion. The usual dosage is from 0.5 to 2.0 per cent. (Undecanoic alkanolamides (alkylolamides) are available from (1) Rewo G. m.b. H. Germany, (2) Dragoco, Germany, (3) Dutton and Reinisch, England).
Hair conditioners are considered to improve the appearance of the hair by giving body and lustre, and to achieve this effect two types of hair conditioning creams are used. The most popular are those used as rinses and are applied to the hair after shampooing and rinsing, whilst the hair is still wet. The second category includes hair dressings or creams, and brilliantines. These are applied to dry hair either immediately after setting and drying, or at any time when extra gloss or light fixing properties are required.
Preparations for Wet Hair
Hair conditioning preparations for use on wet hair after a shampoo are prepared either as creams or lotions. Probably the most successful type are those which contain a quaternary ammonium compound as the active ingredient. Following a shampoo or permanent wave the cream is applied with the hands over towel-dried hair and distributed evenly by combing. If the product is in lotion form this can either be poured over the hair followed by combing, or diluted with water and poured repeatedly over the hair whilst the head is held over a basin. The cream or lotion is left on the hair for a few minutes and then rinsed off with warm water.
Reference has already been made to the bactericidal properties of the quaternary ammonium compounds, but their conditioning properties are caused by the relatively large complex cation which is substantive to protein. The quaternary ammonium compound is absorbed onto the hair fibre from a cream or lotion and is retained on rinsing. This removes the static charge and reduces friction between the individual hair strands. As a result the hair is more manageable and easier to handle during setting. Cationic softening agents are used in the textile industry to improve handling. In a similar manner a thin layer of quaternary ammonium compound acts as a lubricant, gives a feeling of body and improves the handling of hair. These products are used to give lustre to dull looking hair, to overcome frizziness and unmanageability caused by faulty or careless permanent waving, use of harsh shampoos, or excessive bleaching.
Satisfactory preparations can be prepared using stearyl dimethyl benzyl ammonium chloride as the active material. Although compounds containing a stearyl group are less bacteriostatic than for example, lauryl compounds, they have better substantive properties, probably on account of their lower solubility. Dosage per application should be carefully controlled and directions for use should also be given clearly. These are best determined by salon trials which are necessary because a high concentration softens the hair loo much so that it becomes limp and does not retain a set. Most products are made as emulsions or creams with small proportions of fatty materials and an emulsifier. The instructions for use should emphasize the importance of thorough rinsing after the application, or otherwise deposition remaining on the scalp has a similar effect to overdosing.
Procedure: Add the water at a temperature of 75ÂºC gradually to the quaternary compound and monosterarate previously heated to the same temperature. Stir slowly and continuously until all the water has been added. Allow to cool and add the lactic acid and perfume when the temperature is about 35Â°C. The cream can either be applied direct to wet hair or mixed with water before use. In either case the dosage should be calculated to give from 0.5 to 0.75 grammes of active material per application. The above formula gives a thin, pourable cream. The consistency can be modified by varying the proportion of ethylene glycol monostearate.
A firmer product can be made to the following formula. Although cetyl alcohol gives body to the cream, the solids content should be kept to a minimum in order to assist ease of removal of the cream during the rinsing process.
Procedure: Melt together the fatty materials and heat to 70-80ÂºC. Dissolve the quaternary compound in water in a separate container and heat to 70-80ÂºC. Add the aqueous solution to the fatty materials whilst slowly stirring to the avoid incorporation of air. Continue stirring until cold adding perfume during cooling at about 35Â°C.
Directions for use can be given so that one part cream added to Sparts of warm water before use gives the desired quantity of 0.7 grammes of active material per application.
Several quaternary ammonium compounds for use as hair conditioning agents are available commercially. Triton X-400 is based on stearyl dimethyl benzyl ammonium chloride together with an alcohol. A formula using this material is given:
Procedure: Heat part of the water with the cetyl alcohol. Heat the Triton X-400 and add to the mixture with stirring. Stirring is continued for 30 minutes to stabilize the emulsion. Finally dissolve the potassium chloride in the remainder of the water and add to the batch.
Potassium chloride acts as a thickener of Triton X-400. A concentrated form of this compound is also available known as Triton X-400 concentrate (Rohm & Haas Co., Philadelphia 5, Pa.). It contains a minimum of 67 per cent of stearyl dimethyl benzyl ammonium chloride and other catrionic materials to give a total of 82 per cent active material.
Emcol 61 (Emulsol Corp., Chicago 3, III), is a condensation product of a fatty acid and amide. This compound is available as an amber coloured paste containing about 10 per cent active material. It is compatible with sodium alkyl sulphate and can be used in shampoos at a concentration of about 5 per cent.
Arquads (Armour Hess Chemicals Ltd.) is the trade mark for a series of quaternary ammonium salts containing alkyl groups with varying chain lengths. Several compounds in this series are water soluble whilst others are either oil-soluble or water-dispersible.
Acid conditioning creams have largely been replaced by those based on quaternary ammonium compounds. Although the former are still popular with certain sections of the public, this type of cream is probably mainly used in the professional salon, particularly after permanent waving. The cream is also applied with the hands or a comb after washing and rinsing, to towel dried hair. It is left on the hair for a few minutes and finally rinsed off with warm water. The cream is considered to give body to the hair, this effect being largely obtained by the thin residual film of fatty material which remains on the hair. A formula is as follows:
Procedure: Melt together the cetyl alcohol with a small proportion of the water. Prepare a solution of sodium lauryl sulphate in water. Warm and add with gentle stirring to the mix. Continue stirring to form a stable cream and finally add a solution of the citric acid in the remaining water.
Dressing-type conditioners are creams applied to dry hair before setting. Used on dull or brittle hair their purpose is to apply a thin film of oil in order to give a natural looking shine or gloss without any appearance of oiliness. A similar effect is obtained with an aerosol spray of a light oily material such as iso-propyl myristate.
Thus, although often referred to as hair conditioners they are more correctly described as dressings. Conditioning properties are claimed because when used in the correct manner the creams give gloss and shine to dull or brittle hair. Only a small quantity of the cream is applied to the hair from the hands. Alternatively a small amount of cream is liquefied by rubbing on the palm of the hand, and the hairbrush is dipped lightly into the liquefied cream and brushed over the hair. Either method is designed to avoid using an excess of cream which gives the hair an oily or greasy appearance. The amount of cream required to give the best results varies. Fine hair does not need as much cream as coarse hair and it is advisable to draw attention to this point. It follows that water-in-oil emulsions are most suitable for application in this manner. Creams suitable for tube packaging can be made as follows:
Procedure: Melt together the wool alcohols and petroleum jelly. Add the iso-Protyl myristate and mineral oil and heat to 70Â°C. Add the preservatives Heat the water to 70-75ÂºC and add to the oil mixture with stirring Homogenize and allow to cool.
1. Empilan KL 6 type-Albright & Wilson Ltd., Marchon Div.
2. MS 200 type-Midland Silicones Ltd.
Procedure: Melt together the ingredients of part A to a temperature of 75ÂºC and add part B to part A slowly with continuous stirring. Stir until cool adding the perfume when the temperature has fallen to about 35Â°C.
An aerosol hair conditioner for use as a rinse is prepared as follows:
Procedure: Heat part A and part B independently to 75ÂºC. Add B to A slowly with continuous stirring. Cool with stirring, adding the perfume at 30Â°C.
Container: Plastic coated glass. This type of product is known to attack tin plate, therefore rigorous shelf testing is essential before marketing in a metal container. Valve: tilt action fitted with a foam head.
Setting lotions are used both at home and at the hairdressing salon to style the hair. After permanent waving use of a setting lotion enables the hair to hold its shape for several days, and between visits to a hairdressing salon they are often used to pin the hair at night to help brushing out and styling the following morning.
Lotions based on gums and mucilages continue to be popular. The most favoured gum is tragacanth, followed by the cheaper substi-tuteâ€"karaya gum also known as Indian tragacanth. Acacia or gum arabic is less popular, although it has the advantage of easy solubility. Mucilages prepared by decoction of quince seeds, psyllium seeds, and irish moss can also be used. The mucilages prepared from gums are generally prepared as weakly alcoholic solutions and the decoctions are used as aqueous solutions. Both types of lotion are coloured and perfumed, and must contain an adequate amount of preservative. It is not desirable to lay down any hard and fast rules as to the strengths of the various setting lotions because a good deal depends upon the type of hair and individual preference. In particular, mucilages prepared with gum tragacanth very considerably depending on the quality of the gum used. The percentage margins are, however, approximately as follows:
Procedure: for preparing mucilages: in the case of tragacanth and karaya gums the alcohol, preservative and perfume are mixed with the powdered gum and the water added in a continuous stream to facilitate even distribution and swelling. In the case of quince and psyllium seeds hot decoction for ten minutes is sufficient followed by straining and cooling. Irish moss is infused cold for a lew hours after being freed fro extraneous matter by washing. All the other constituents are merely dissolved or mixed as the case may be.
The alcohol used for wetting purposes to prepare the mucilaginous products also reduces drying time of the lotion in use. From 2 to 5 per cent of glycerin can also be included in the formula and other suitable additives include 0.1 per cent of cholesterol or 1 to 2.5 per cent of a water-soluble lanolin or lanolin derivative. A formula for a setting lotion of this type is as follows:
1. Solulan 98 typeâ€"American Cholesterol Products Inc.
Procedure: Dissolve the preservative in the glycerin using gentle heat. Add the tragacanth and cholesterol; mix to a smooth paste. Mix the water, water soluble lanolin, and perfume separately and add to the tragacanth mixture using vigorous sgrring to commence. Allow to stand before filling out. Alcohol (about 5.0 per cent) can be included to disperse the tragacanth before adding the glycerin. Add a suitable water-soluble dyestuff.
A carboxy vinyl polymer is used to prepare an attractive transparent gel used for setting the hair. The product is easy to handle and more attractive than a mucilage. Polyvinyl pyrroliclone or a co-polymer is included as a film former. A suitable products is made to the following formula:
1. Carbopol 940 typeâ€"B.F. Goodrich Chemical Co.
Procedure: Dissolve the polyvinyl pyrrolidone and preservative in the alcohol. Disperse the polymer in the triethanolamine and gradually add the water with stirring. Add the alcohol solution and perfume.
Polyvinyl pyrrolidone co-polymers and other resinous materials already mentioned have, to a large extent, replaced setting lotions based on gums and colloids. Aqueous lotions of polyvinyl pyrrolidone are quite pliable after application so that the hair can easily be set before drying. On drying a transparent film is formed which gives body and firmness depending upon the concentration used in the lotion.
In order to prevent the dried PVP film from flaking a plasticizer is used such as a water soluble lanolin or a glycol. Diethylene glycol is particularly suitable since it helps to form a dry film. The concentration of plasticizer should be 10 per cent of the PVP content of the lotion. Suitable formulae are as follows:
Use a water-soluble perfume and add a suitable water-soluble dye-stuff.
This lotion has a slightly acidic pH value and addition of an alkali to a pH value of about 9.0 causes softening and slight swelling of the hair fibre and increases penetration of the PVP. An alkaline lotion is thus considered to give a more firm and lasting set. With this type of product, on account of the residual PVP film, if the hair is wetted slightly with water om subsequent days after use it can be restyled and set without a further application of the lotion.
When using aqueous alcoholic solutions of PVP the dried PVP film has a tendency to flake when the hair is subsequently combed, and although the degree of flaking is reduced when the correct glycol is used as the plasticizer. even less flaking occurs when a small proportion of an ethylene oxide condensate is included in the formula.
1. Empilan KL (5 or KL 10 type-AIbright & Wilson Ltd.
Use a water-soluble perfume and include a suitable watersoluble dyestuff.
Polyvinyl pyrrolidone co-polymers are used a similar fashion. Their use is sometimes preferred because the residual film remains more stable in conditions of high humidity. A good product is prepared as follows:
Add an alcohol and water-soluble perfume.
Procedure: Dissolve the PVP: VA in the alcohol with stirring. Add the perfume and iso-propyl myristate. Slowly add the water, stirring constantly.
A pearly setting lotion based on stearic acid is made as follows:
Procedure: Gently heat all the ingredients together and stir until a smooth gel is formed. To prepare the setting lotion dilute 5 parts of the base with 95 parts of water. Include methyl parahydroxybenzoate 0.15 per cent. Use a water-soluble perfume and a suitable water-soluble dyestuff.
Good results are also obtained with dimethyl hydantoin formaldehyde resin, as indicated in the following formula:
Procedure: Dissolve the resin in the alcohol with stirring. Add the iso-Propyl alcohol and diethyl phthalate. Add the perfume, followed by the glycerine and water, and mix. A water-soluble dyestuff can be added.
Coloured setting lotions used as temporary colourants are made by adding certified soluble dyestuffs to a suitable setting lotion base. The dyestuffs used are mainly alcohol-soluble types although certain water-soluble dyestuffs and others which are both oil and alcohol soluble are also suitable. The solvent of the setting lotion base must therefore be adapted to suit the solubility characteristics of a particular dyestuff used to achieve the desired colour effect. Coloured setting lotions are used by the professional hairdresser and also sold in one application packs for the home user. A note regarding their preparation is also given in the next section dealing with aerosol temporary colours.
Aerosol Setting Lotions
Aerosol setting lotions are convenient to handle as they prevent dripping and spilling of the liquid in use. The dried film on the hair must not be too brittle otherwise when the set is combed out the film breaks, causing dust particles to cling to the comb and make the hair look dull and lifeless. The following formula gives very good results:
Procedure: Dissolve A with continuous stirring, and add B. Mix together C and add to the bulk. Mix with stirring, and finally mix the perfume with D and mix.
Container: internally lacquered aluminium or tin plate. Valve: standard fitted with a button similar to that used for hair sprays.
If a conditioning agent is required in the above formula then the addition of 0.5 per cent cetyl trimethyl ammonium bromide is recommended. In this case, however, it is not advisable to pack in a metal container without shelf testing, as cetyl trimethyl ammonium bromide can attack tin plate in certain conditions.
Valve: tilt action with a micro mist actuator.
Hair Lacquers or Sprays
Hair lacquers or hair sprays are used on the hair after setting and are intended to hold the style firmly in shape without detracting in any way from the artistic finis. Apart from a satisfactory formulation the appearance of the finished pack, the use characteristics and choice of perfume often contribute to the success of a product. They consist of a film-forming material in a suitable solvent together with a plas-ticizer or modifier to promote flexibility of the resin. The basic composition is given as follows:
1. Film- former
2. Plasticizer (modifier)
Shellac was invariably used as the film-former in early formulations. This resin is secreted from a scale insect and deposited on the twigs of various trees in India, Siam, and Indo-China. The resin entrusted twigs which are collected from the trees are known as â€˜stick lac.â€TM When this has been ground and washed it is known as â€˜seed lacâ€TM and the shellac of commerce is prepared from this material by melting and straining or by solvent extraction. It contains about 95 per cent of resinous substances including alevritic, shelloic, kerrolic, and butolic acids. For use in hair lacquers, the refined quality known as palest dewaxed flake shellac should be used. The flakes are prepared by pouring the melted resin over plates or cylinders and as the resin hardens it scales off in thin flakes. Shellac is insoluble in water, but dissolves readily in warm alcohol. iso-Propyl alcohol is the best solvent and can be used to prepare solutions containing up to 25 per cent of the resin. A solution of this strength is a convenient method of storing the resin in the form of a concentrate available for dilution as and when required. Although shellac is considered by many to be inferior to other film formers which are now available, it is still used for fantasy hair styling particularly by the professional hairdressers, when a high degree of fixation is required. It gives a rigid film which tends to break when handled even though plasticiz-ers or modifiers are used. The resin is also difficult to remove from the hair and often causes flaking when the hair is subsequently brushed or combed. In addition, when a shellac film is used on the hair it cannot be wetted with water and restyled. On the other hand a shellac film is not affected by humidity and holds the hair in position for long periods.
The film obtained with a shellac-type hair lacquer can be controlled to a large extent by the amount and type of modifier or plasticizer used.
A typical formula is as follows:
A shellac film which is more water-dispersible can be obtained by the addition of an alkali illustrated by the following formula.
Procedure: Dissolve the perfume in the alcohol and dissolve the shellac in the mixture. Mix the triethanolamine with the water and add the alcoholic solution slowly with constant stirring.
It is important to consider the time of drying when formulating a hair spray, and this will naturally take longer when the product includes water.
Selection of a suitable perfume plays an important part in the success of all hair sprays. It must remain stable in note and intensity of odour. Unless the hair spray is one of a range of perfumed products containing a specific perfume it should be of a light and fugitive character so that it docs not clash, but preferably blends with the users normal perfume.
With formulations which require a water-soluble perfume, the properties of the spray should be checked both with and without the perfume to determine the effect of the solubilizer which has been used. Some perfume solubilizers act as plasticizers and affect the properties of the film on the hair. Mention has already been made of the effect of both amount and type of modifier or plasticizer on the properties of a resinous film on the hair. This applies particularly with shellac based sprays and the table which follows gives an indication of some of the different effects which are obtained.
In assessing the properties of the films on the hair with the formulations given in Table 1 the extent of gloss is given as determined by visual examination. A standard procedure of combing the dried film is used to give a measure of the degree of flaking. Maximum flaking is indicated by the figure â€˜100â€TM and occurs when no plasticizer is used.
The results of the practical tests illustrated in Table 6.1 indicate the value of carrying out tests with various concentrations of shellac and modifier before deciding on a particular formulation.
Polyvinyl pyrrolidone or PVP is a popular material for the formulation of hair sprays. It is a synthetic polymer first used during World War II as a blood plasma extender, as was initially prepared by the action of acetylene on formaldehyde at high pressure. It is non-toxic and neither a primary skin irritant nor sensitizer.
The polymer is used to prepare aqueous solutions of different viscosities, the grades available being denoted by a K value. This is a function used to define the molecular weight of the product as related to the viscosity of a 1.0 per cent aqueous solution. Three viscosity grades are availableâ€"K30, K60, and K90, but the material normally used for the preparation of hair sprays is the low viscosity grade with a K value of 30 (30-35). In solid form the material is a white or off-white hygroscopic powder and as generally supplied contains about 5 per cent water.
If the material is required for products which must not contain appreciable amounts of water this should be specified to the suppliers. In this case PVP is packed hot in heat sealed polythene containers immediately it is recovered from the drying plant. This form normally contains from 1.0 to 1.5 per cent of water. Although packaged in moisture-proof containers it readily picks up moisture once the container is opened, and can become sticky and difficult to handle. For this reason it is often convenient to obtain supplies in solution form. These solutions keep satisfactorily, provided they contain a suitable preservative. Aqueous solutions which are quite stable can be obtained containing about 30 per cent of solid material. This solution has a specific gravity of 1.07, is pale yellow and slightly viscous in appearance and has a slight characteristic, odour. In addition to being miscible with water, polyvinyl pyrrolidone is soluble in many organic solvents including some esters and fatty acids and a wide range of alcohols.
The solubility properties make PVP a versatile raw material and its use is referred to in the formulation of shampoos, creams, aftershave lotions, and shaving cream, in addition to its use in hair setting lotions and hair sprays.
Hair lacquers based on PVP can therefore be prepared either with all alcohol or water or aqueous/alcoholic solutions as the solvent, and they can easily be removed by shampooing. Lacquers prepared without water enhances the appearance and give a so-called conditioning effect which is more apparent than those containing water. This is probably due to a more even distribution and greater penetration of PVP into the hair shaft during the particular condition of usage. They give a soft and pliable set which is firm but not stiff or rigid like the shellac film and after use the hair can be reset by wetting with a small amount of water using a brush or comb. The PVP film is, however, somewhat brittle when used on its own and use of suitable modification or plasticixer is recommended. The fact that the polymer is hygroscopic is a disadvantage in conditions of high humidity. These cause the set to fall and the hair to become quite sticky. Better results are obtained by including in the formula a small proportion of a material to act as a water repellent. Several materials have been recommended for use as plasticix.ers with PVP including dimethyl, diethyl and dibutyl phthalates, iso-Propyl myristate and certain lanolin derivatives.
When formulating a PVP lacquer, it is important to examine the effect of various concentrations of the plasticixer not only in relation to the pliability of the lacquer film, but also to the effect obtained when the hair is subsequently brushed or combed. Used on its own the PVP film causes flaking, so the best plasticixer is one which can be used at a concentration which does not affect the particular rigidity required and at the same time will give the least amount of flaking. In this case the plasticixer is not used primarily to soften the film but rather to improve its adherence to the hair and prevent flaking. If too much plasticixer is used the PVP film tends to become sticky.
Table 6.2 indicates the effect of several plasticixers when they are used with PVP at various concentrations and the results are shown in a similar manner to those given by shellac films.
It will be seen that 2.5 per cent PVP arid 2.0 per cent propylene glycol monolaurate gives a firm film with a better gloss than that obtained using diethyl phthalate. No flaking occurred on combing in either case. If the concentration of PVP is increased to 7.5 per cent, the same proportion (2.0 per cent) of propylene glycol monolaurate still gives a firm film with a good gloss but causes flaking on combing, whereas no flaking occurs in this case with diethyl phthalate.
The results do indicate that effective lacquer systems can be prepared with a range of concentrations of PVP provided the effect of the plasticizer is checked carefully. To increase the water repellency of PVP lacquers small proportions of shellac, silicone oil, or certain modified resins can be included. As shown in the table it will be seen that by using 10 per cent of silicone oil based on the PVP content a rigid film is obtained although this flakes when combed. The degree of flaking can be reduced if a pththalate is added as the plasticizer to the system.
It does not follow that water repellency is always required. Where climatic conditions are dry a small percentage of a humectant is used to prevent any drying effect on the hair caused by using PVP (Brit. Pat. 747806). Examples of formulations for lacquers based on PVP are given.
Preparation of the lacquers is a staightforward procedure. The PVP is dissolved in the alcohol and any additives added and mixed until solution is effected. The perfume is then added and the lacquer is allowed to stand and finally filtered before filling.
The above formula gives a firm but flexible film which does not flake. It is particularly effective on fine hair.
This lacquer is suitable for use on coarse or â€˜wiryâ€TM hair which are more difficult to control, or on fine hair if a good fixative is required.
Reference has already been made to the effect of a solubilizer when a water-soluble perfume is used in a lacquer system. It is equally important to check the properties of a lacquer formulation with and without perfume when a perfume concentrate is being used in an alcohol based lacquer. Some perfumes contain phthalates and will effect the properties of the film. In some circumstances a phthalate is also required to be used as a denaturant for the alcohol and adjustment of the formula must be made to allow for this.
Precipitation of PVP can also occur due to reaction with certain raw materials used in compounding perfumes, and it is advisable to check that this does not occur with any other cosmetic products containing PVP.
Although it is useful to include lanolin or a lanolin derivative in a lacquer as a selling point, tests show that when these materials are used as the sole plasticizer they tend to improve the flexibility of a PVP film and reduce the hygroscopicity but do not prevent flaking. For this reason they are best used in small amounts only together with a phthalate.
Suitable alcohol soluble derivatives include Acetulan, Amerchol L-101, and Lanethyl. It should be noted that the total amount of plasticizer used is usually from 10 to 12 per cent of the resin content.
Lacquers are also presented to give special effects with soft flexible films for casual wave effects. One way of obtaining this effect is to use a higher concentration of plasticizer. The following formula gives a soft film with a good gloss.
When an aqueous/alcoholic solution is used as the vehicle this naturally extends the drying time of the lacquer. This type of product is less expensive to produce and is useful for the professional hairdresser when the hair is dried by heat after setting. It is also sold as a lacquer and setting lotion combined and the properties and uses are described according to the proportions of water and alcohol used in the formula. In particular the lotion is suitable to apply to damp hair after shampooing. In this case the hair is set with rollers or by pin-curlers and after setting is allowed to dry and then combed out. The spray can then be used again to keep the hair in place. A suitable product can be prepared as follows:
Co-polymers of polyvinyl pyrrolidone and polyvinyl acetate have different properties to PVP partly due to the plasticizing effect of the acetate. These materials, generally referred to as PVP/VA co-polymers, give films suitable for use as hair sprays, particularly because they do not pick up moisture as readily as PVP. The resins are prepared with different proportions of acetate as shown:
Since the acetate exerts a plasticizing effect the proportion of acetate present in the co-polymer affects the type of film obtained on the hair. If the proportion of acetate is too high the lacquer film does not bind onto the hair shaft. The PVP/VA 60:40 co-polymer gives a satisfactory firm film which is made more flexible by using a suitable plasticizer. Although the film on the hair is not affected by humidity to the same extent as a PVP film the lacquer will become soft and sticky if the proportion of modifier used in the formula is too high.
Diethyl and dimethyl phthalates, and polyethylene glycol 400 are suitable plasticizers for the PVP/VA film. These materials are used at a concentration of 10 per cent of the amount of co-polymer.
A soft flexible film can be obtained by including iso-Propyl myristate. in this instance to give softness and added gloss or lustre to the hair.
Solutions of the resin or the completed spray solution should be filtered before packaging, preferably after standing overnight in suitable closed containers.
Dimethyl hydantoin formaldehyde resin (DMHF) (Rex Campbell & Co. Ltd.) is a light coloured brittle material soluble in both alcohol and water. Used as the film-former of hair sprays the compound gives soft, firm or rigid films, depending upon the concentration used. It is less hygroscopic than either PVP or PVP/VA co-polymers and when used with the correct amount and type of plasticizer gives a non-tacky film and a good gloss to hair. Solutions in alcohol are more easily prepared with the aid of gentle heat.
Suitable plasticizers for use with DMHF resin are as follows:
1. Alcohol-soluble lanolin derivatives: (or water-soluble depending upon the solvent system used)
2. Propylene glycol monomyristate:
3. Diethyl or dimethyl phthalate:
4. iso-Propyl myristate.
Using 10 per cent of any of these plasticizers based on the content of resin, firm lacquer films are formed which show good gloss and do not flake when the hair is combed. If the amount of plasticizer is increased to 20 per cent the films obtained with soluble lanolin derivatives and diethyl phthalate become sticky, and the film obtained with propylene glycol monomyristate has less gloss. The types of lacquers obtained using various concentrations of resin with different plasticizers are shown as follows:
Lacquers based on the proportions of resin and plasticizer given above all give a good gloss to the hair and do not cause flaking. The lacquers are prepared by first dissolving the resin in the solvent. The remaining ingredients are then mixed with the solution which is allowed to stand overnight in suitable closed containers. The solution is filtered before filling out.
DMHF resin is used with a small proportion of shellac to prepare a spray suitable for use on difficult or â€˜hard-to-holdâ€TM hair. The resin is also useful to include in sprays based on PVP or PVP/VA to reduce hygroscopicity.
Dantoin 693 (Rex Campbell & Co. Ltd.) is a modified dimethyl hydantoin terpolymer resin free from formaldehyde and is used in a similar way to dimethyl hydantoin formaldehyde resin. It is non-hygroscopic and forms a good flexible film which is completely removed from the hair by shampooing.
Resin 28-1310 (National Adhesives and Resins Ltd.) is a vinyl acetate co-polymer and Resin 28-3307 is a carboxylated vinyl acetate co-polymer including a co-polymerized ultra-violet light absorber. These materials are available as fine transparent beads which are soluble in alcohol and chlorinated solvents, the latter being used as a co-solvent for concentrated solutions. Partial or complete alkali neutralization of alcoholic solutions with amino hydroxycompounds determines the final water solubility, complete water solubility being obtained with 100 per cent neutralization. Thus hard spray films with poor water solubility are obtained by 10 to 70 per cent neutralization and softer more water-soluble films by 80 to 90 per cent neutralization of the resin. Consequently the properties of the resin film can be varied to suit conditions to provide specific properties by controlling the degree of neutralization. The most suitable neutralizers are AMPD, 2-amino-2 methyl-1,3 propanediol and AMP, 2-amino-2 methyl-1 propanol.
Further modifications of the film are obtained by using plasticiz-ing additives such as lanolin, dimethyl pththalate and iso-propylmyristate, as already indicated in the previous text.
It seems likely that new resins will become available to provide specific properties to hair sprays. Amongst the several available at the present time polyvinyl imidazone (PVI) (U.S. Patent 2953498) is a resin of similar chemical structure to PVP. This material is soluble in both alcohol and water, and gives films which do not become tacky at high relative humidities. The films are flexible and can be used without special additives and modifiers.
Polymers prepared from N-vinyl oxazolidones (Devlex-Dow Chemical Co.) are available either as water or alcohol soluble materials suitable for formulation of hair sprays and setting lotions. Gantrezhan (General Aniline & Film Corp.) is a co-polymer of vinyl methyl ether and maleic anhydride, suitable for application in water based hair sprays and setting lotions.
Consumer research inevitably controls the type of product required by the public and this applies particularly to the properties of hair sprays. Products should be carefully formulated and evaluated to provide the particular properties required. As a general guide to performance the hair-spray should provide sufficient adhesion and control and be easy to remove from the hair; it should not become sticky or greasy in conditions of high humidity and should not flake, dry, or dull the hair. The spray can be prepared for its hair controlling properties only, as a dual purpose setting and fixing lotion or for condi-iioning effect to give the hair lustre and gloss and maintain a soft, natural looking set.
Complete formulations for aerosol hair sprays are now given based on the materials discussed in the previous text. The following formulation has been found to give good results and washes out completely by shampooing:
Procedure: Dissolve the polyvinyl pyrrolidone in the alcohol. Stir well and add the propylene glycol monomyristate and perfume. Mix well.
Container: internally lacquered tin plate or aluminium. Valve: standard with lacquered cup.
The following formula gives good holding properties to the hair with a good gloss and is easily washed out by shampooing:
Procedure: Dissolve the PVP:VA in the alcohol with stirring. Add the rest of the raw materials and the perfume. Mix well.
Container: internally lacquered tin plate or aluminium. Valve: standard with lacquered cup.
Dimethyl hydantoin formaldehyde resin can be used in a range of formulae from â€˜soft holdâ€TM sprays to â€˜firm holdâ€TM sprays, and is readily removed by shampooing. A â€˜firm holdâ€TM spray is obtained with the following formula:
Procedure: Dissolve the DMHF resin in the alcohol. Add the perfume and iso-Propyl myristate and mix well.
Container: internally lacquered tin plate or aluminium. Valve: standard with lacquered cup.
To increase the hardness of the film on the hair 0.5 per cent of palest dewaxed shellac can be added to the above formula. The film will still shampoo out of the hair satisfactorily. To give a softer film on the hair reduce the percentage of DMHF to about 3.0 percent.
Container: internally lacquered tin plate or aluminium. Valve: standard with lacquered cup.
Procedure: Dissolve the Dantoin resin 693 in half the amount of iso-Propylalcohol with gentle heat, stirring occasionally. Cool, add the remainder of the iso-Propyl alcohol, the iso-Propyl myristate and the perfume. Mix well.
Containeninternally lacquered tin plate or aluminium.Valve:standard with lacquered cup.
This formula can also be made using ethyl alcohol instead of iso-Propyl alcohol, and the perfume content can then be reduced to between 0.2 and 0.5 per cent.
Procedure: Dissolve the AMPD and Resin 28-1310 in the alcohol with stirring. Add the iso-Propyl myristate and perfume. Mix well.
Container: internally lacquered aluminium or tin plate. Valve: standard with lacquered cup.
The above formula is also suitable for use as a manâ€TMs hair fixative.
The most rigid film former used in hair spray formulations is, of course, shellac. It has the biggest disadvantage, that of being insoluble in water. A hard and rigid hair spray film based on shellac is made as follows:
Procedure: Dissolve the shellac in the alcohol with continuous stirring, care being taken not to stop stirring until all the shellac has been dissolved, otherwise the shellac will sink to the bottom of the reactor and stick as a resinous mass. Finally, when dissolved add the diethyl phthalate and perfume.
Container: internally lacquered aluminium or tin plate. Valve: standard with lacquered cup.
Use of Resin 28-3307 and the effect of neutralization with 2-amino-2 methyl-1,3 propanediol (AMPD) is shown in the following three formulations. Hair sprays of â€˜softâ€TM, â€˜regularâ€TM, and â€˜hard-to-holdâ€TM residual films are obtained by varying the proportion of resin neutralizing agent and plasticizer or modifier. The sprays give good gloss to the hair, do not show any dust after combing, and are easily removed by shampooing.
Procedure: Weigh out the alcohol into a mixing vessel fitted with a variable speed stirrer. Add the perfume, AMPD, and iso-Propyl palmitate. Commence stirring fairly rapidly and slowly add the Resin 28-3307 beads. Continue stirring until the beads have completely dissolved.
Container: internally lacquered aluminium or tin plate. Valve: standard.