82 JOURNAL OF THE SOCIETY OF COSMETIC CHEMISTS REFERENCES (1) M. Saitoh, M. Uzuka, M. Sakamoto, and I. Kobori, "Rate of Hair Growth," in Advances in Biology of Skin, Vol. IX, Hair Growth, H. Montagna and R. Dobson, Eds. (Pergamon Press, New York), pp. 183-200. (2) C. A. Burgess and C. R. W. Edwards, Hirsutography, Br. J. Photography, 8, 770-772 (1978). (3) D. R. Harkhess and H. A. Bern, Radioautographic studies of hair growth in the mouse, Acta Anato- mica, 31, 35-39 (1957). (4) D. Jackson and F. J. Ebling, The guinea pig hair follicle as an object for experimental observation. J. Soc. Cosmet. Chem., 22, 701-710 (1971). (5) D. D. Munro, Hair growth measurement using intradermal sulfur 35-cystine, Arch. Dermatol., 93, 119-122 (1966). (6) H. L. Dawson, A study of hair growth in the guinea pig (Cavia cobaya), Am. J. Anat., 45, 461-480 (1930). (7) S. Chen, H. Nakamura, and Z. Tamura, Studies on the metabolites of fluorescein in rabbit and human urine, Chem. Pharm. Bull., 28, 1403-1407 (1980). (8) J. S. H. Jacob, E. D. Rosen, and E. Young, Report on the presence of a toxic substance, dimethyl formamide, in sodium fluorescein used for fluorescein angiography, Br. J. Opthalmol., 66, 567-568 (1982). (9) J. B. McCraw, B. Myers, and K. D. Shanklin, The value of fluorescein in predicting the viability of arterialized flaps, Plast. Reconstr. Surg., 60, 710-715 (1977). (10) M. Araie, M. Sawa, S. Nagataki, and S. Mishima, Aqueous humour dynamics in man as studied by oral fluorescein, Jpn. J. Opthalmol., 24, 346-362 (1980).
J. Soc. Cosmet. Chem., 38, 83-98 (March/April 1987) Effects of some cosmetic pigments on the bactericidal activities of preservatives TETSUO SAKAMOTO, MITSUO YANAGI, SHOJI FUKUSHIMA, and TAKEO MITSUI, Shiseido Laboratories, 1050, Nippa-cho, Kohoku-ku, Yokohama-shi, 223 Japan. Received September 13, 1982. Presented at the Annual Seminar of the Society of Cosmetic Chemists, Memphis, Tennessee, May I3, I982. Synopsis The effects of eight cosmetic pigments on the bactericidal activities of p-hydroxybenzoic acid esters (methyl through butyl) were investigated by a viable cell count method. Most of the tested pigments interfered with the bactericidal action of all four perservatives. The degree of inactivation was highest for ultramarine blue followed by talc, titanium dioxide (R), titanium dioxide (A), red oxide of iron, and yellow oxide of iron. In general, the bactericidal activity of methyl p-hydroxybenzoate was affected the least. The mechanism of inactivation was also investigated. The lack of a phenolic hydrogen for inactivated methyl p-hydroxybenzoate was demonstrated by •H-NMR analysis. It is likely that the phenolic hydrogen of methyl p-hydroxybenzoate was replaced by some metal from the coexistent pigments. This is postulated to be the inactivation mechanism. The addition of EDTA prevented the inactivating action. INTRODUCTION Microbial contamination of non-sterile cosmetic formulations has recently drawn con- siderable attention. A number of suggestions have been put forward to overcome such problems (1-3). The addition of properly selected preservatives is of special impor- tance, particularly in dealing with contamination during use. A key factor to be consid- ered in the choice of a proper preservative is the interaction between the particular germicide and the ingredients of the formulation. Although many cosmetic materials, especially surfactants, have been shown to interact with a number of preservatives (4-6), the direct microbiological consequences of such interactions are not fully catalogued. Information, concerning the effects of cosmetic pigments on the bactericidal activities of preservatives, is rarely found. The present investigation deals with the effects of various cosmetic pigments on the bactericidal activities of four commonly used preser- vatives. 83
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