Journal of Cosmetic Science

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J. Cosmet. Sci., 56, 1-16 (January/February 2005)

Characterization of the lipid composition at the proximal root regions of human hair

YOSHINORI MASUKAWA, HIROFUMI NARITA, and GENJI IMOKAWA, Tochigi Research Laboratories, Kao Corporation, 2606 Akabane, Ichikai, Haga, Tochigi, 321-3497 Japan.

Accepted for publication December 3, 2004.

Synopsis
The hair lipid composition collected from 44 Japanese females between 1 and 81 years of age was examined for eight lipids including hydrocarbons (HCs), squalene (SQ), wax esters (WEs), triglycerides (TGs), fatty acids (FAs), cholesterol (CH), ceramides (CERs), and 18-methyl eicosanoic acid (MEA). In this study, the 5-cm length from the proximal root end of hair fibers, which had never been exposed to any chemical treatment, was used after 5-min incubation with hexane following shampooing. Hair lipids were extracted with solvent and subsequent alkali-solvent and were then analyzed by a combination of chromatography. Although the average contents of the lipids showed great fluctuations among individuals, there were significant correlations between the levels of each lipid, which allowed for the classification of the hair lipids into four groups: group A: SQ, WEs, TGs, and FAs (designated as endogenous lipids based upon their sebum origin); group B: CH and CERs (designated as endogenous lipids); group C: HC (unknown origin); and group D: MEA (the other endogenous lipid). A principal component analysis for eight lipids revealed that the hair lipid composition was characterized by a predominant negative correlation between each lipid for groups A and B. This negative correlation suggests that the endogenous lipids in group B serve as a barrier against the penetration of predominantly sebum-derived exogenous lipids (group A). Endogenous lipids consisting of CH and CERs (group B) and MEA (group D) should be designated as intrinsic internal lipids of human hair.


J. Cosmet. Sci., 56, 17-27 (January/February 2005)

L-Ergothioneine scavenges superoxide and singlet oxygen and suppresses TNF-_ and MMP-1 expression in UV-irradiated human dermal fibroblasts

KEI OBAYASHI, KOUJI KURIHARA, YURI OKANO, HITOSHI MASAKI, and DANIEL B. YAROSH, Cosmos Technical Center Co. Ltd., 3-24-3, Hasune, Itabashi-ku, Tokyo, 174-0046 Japan (K.O., K.K., Y.O., H.M.), and AGI Dermatics, 205 Buffalo Avenue, Freeport, NY 11520-4709 (D.B.Y.).

Accepted for publication November 16, 2004.

Synopsis
Ergothioneine (EGT) is a sulfur-containing amino acid, and is presumed to function as a natural antioxidant. The purpose of this study was to identify the nature of the antioxidant activity and investigate the effects of EGT on UV-induced cellular response. In chemical studies, EGT scavenged the superoxide anion radical (oO2 -) and singlet oxygen (1O2). In cultured fibroblasts, EGT suppressed TNF-_ up-regulation by UVB irradiation. In addition, in fibroblasts exposed to UV-A, EGT suppressed the expression of matrix metalloproteinase 1 (MMP-1) protein by nearly 50% and reduced MMP-1 mRNA expression. From these results, we conclude that EGT scavenges reactive oxygen species generated by both Type I and Type II photosensitization and suppresses both TNF-_ expression and MMP-1 at their transcriptional level. EGT may reduce skin anti-aging effects after UV irradiation by the scavenging of oO2 - and 1O2, and reducing signals for protease and inflammatory activity.


J. Cosmet. Sci., 56, 29-46 (January/February 2005)

A novel "permanent" acid-type hair color made possible with dye-metal ion complex technology

M. OCHIAI, T. KAWASOE, M. YASUDA, Y. HARADA, T. KIMURA, T. KAMBE, and J. KURITA, Product Development Center (M.O., T. Ka., Y.H., T. Kam.), Basic Research Center (M.Y., T. Ki.), and Institute of Beauty Science (J. K.), Shiseido Co., Ltd., 2-2-1 Hayabuchi, Tsuzuki-ku, Yokohama-shi, 224-8558 Japan.

Accepted for publication December 14, 2004.

Presented in part at the 22nd Congress of the International Federation of the Societies of Cosmetic Chemists (IFSCC), Edinburgh, Scotland, September 26, 2002.

Synopsis
The advantages and disadvantages of oxidative permanent and acid-type semi-permanent hair colors are evident. The former provides a longlasting "permanent" color, while the latter imparts less damage to the hair. We developed a novel acid-type hair color technology that can allow an acid dye and a metal ion to form a complex inside the hair similar to the oxidative hair color. It is well known that acid dye diffuses into the hair and creates an ionic bond with the positively charged amino acid residues of hair protein. However, the dye can be extracted easily from the hair by daily shampooing due to the weakness of the bond. In order to strengthen this bond and to prevent the extraction of the dye by shampooing, an aluminum chloride ion was chosen as the metal ion component to form the dye-metal complex. A proper composition of penetration enhancers, benzyl alcohol and ethyl alcohol, was required to allow acid dyes to interact with the aluminum chloride ion after each component penetrates deeply into the hair to form a complex inside the hair. To provide color brightness and a color longevity effect to hair color, glycolic acid was also selected due to the observation that a weak acid with a small molecular weight would enhance those effects.


J. Cosmet. Sci., 56, 47-56 (January/February 2005)

A study of the photolightening mechanism of red hair with visible and ultraviolet light: Comparison with blond hair

T. TAKAHASHI and K. NAKAMURA, Kao Corporation, Hair-Care Research Laboratories, 1-3, Bunka 2, Sumida-ku, Tokyo, 131-8501 Japan.

Accepted for publication December 9, 2004.

Synopsis
The photolightening behavior of red hair was investigated. Red hair was found to lighten to a similar extent by irradiation from both ultraviolet (UV) and visible (VIS) light. Under the same irradiating conditions, blond hair was lightened by VIS light but did not lighten by UV light until it was washed after irradiation (1). These different photolightening behaviors of red and blond hair are supposed to be due to differences in their melanin compositions. The dominant type of melanin in red hair is pheomelanin; while blond hair investigated in the previous work contained both eumelanin and pheomelanin, with mainly eumelanin (2). Consequently, in this investigation, the photolightening behaviors of red and blond hair were compared to clarify the differences in photosensitivity between the two types of melanin. It has been proven that chemically intact melanin in red hair is considerably more photolabile to UV light than VIS light. Also, it is much more easily decomposed by UV light than melanin granules in blond hair, although they are both similarly decomposed by VIS light. This indicates that pheomelanin is far more sensitive to UV light than eumelanin, while these two types of melanin are similarly sensitive to VIS light. This leads to the following hypothetical photolightening mechanism of red hair: When UV light is irradiated on red hair, the light is absorbed by hair protein and attenuated before it reaches the melanin granules. However, since pheomelanin is highly sensitive to UV light, even the attenuated UV light decomposes the pheomelanin to some extent. As a result, UV light lightens red hair without the need for subsequent washing, in contrast to blond hair, which consists of mainly eumelanin.


J. Cosmet. Sci., 56, 57-58 (January/February 2005)

Abstracts Journal of the Society of Cosmetic Chemists Japan Vol. 38, No. 3, 2004* * These abstracts appear as they were originally published. They have not been edited by the Journal of Cosmetic Science.


J. Cosmet. Sci., 56, 59-61 (January/February 2005)

Abstracts International Journal of Cosmetic Science Vol. 26, No. 5, 2004* * These abstracts appear as they were originally published. They have not been edited by the Journal of Cosmetic Science.


J. Cosmet. Sci., 56, 63-64 (January/February 2005)

Abstracts IFSCC Magazine Vol. 7, No. 4, 2004* * These abstracts appear as they were originally published. They have not been edited by the Journal of Cosmetic Science.


J. Cosmet. Sci., 56, 65-77 (January/February 2005)

Electron spectroscopy and microscopy applied to chemical and structural analysis of hair

B. C. BEARD, A. JOHNSON, F. M. CAMBRIA, and P. N. TRINH, Akzo Nobel Surfactants America, Akzo Nobel Chemicals, 1 Livingstone Ave., Dobbs Ferry, NY 10522.

Synopsis
The application of surface specific x-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) will be shown to be an effective means for the elucidation of hair fiber surface chemistry and structure. Example studies of bleaching and fiber conditioning treatments are discussed. The bleached fiber surface is found to become more hydrophilic due to the loss of the naturally occurring hydrocarbon overlayer and oxidation of surface functional groups as a result of bleaching. Comparison between generic bleaching regimens illustrates the importance of increased pH and the presence of surfactant for effective treatment. Adsorption of conditioning diester quat and dimethicone molecules reintroduces a hydrophobic like surface layer on the hair fiber. Spectroscopic data indicates a segregated adsorption structure of the chemically different conditioning molecules. Electron microscope Images of the conditioned hair shows a smooth uniform surface.

 

 

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