2004 ANNUAL SCIENTIFIC SEMINAR 413 In a typical TEA Stearate Lotion formulation, three anti-microbial monoglycerides were evaluated in a challenge test (USP 51 "Antimicrobial Effectiveness Testing") against a blend of 0.2% Methylparaben and 0.1 % Propylparaben or against 0.4% DMDM Hydantoin. The individual esters were tested at 0.5%, which is the recommended minimum usage level. E. coli S. aureus A. niger C. albicans Propylene ✓ ✓ ✓ ✓ Glycol Heptanoate Outperformed Outperformed parabens Zero Growth. Outperformed @0.5%in Parabens@ @ 0.3% or DMDM Equal to O .3 % 0.4%DMDM lotion 0.3% Hydantoin@0.4% parabens or DMDM Hydantoin Hydantoin@0.4% Propylene ✓ ✓ Glycol Caprylate Outperformed Outperformed Parabens Performance Performance @0.5%in Parabens@ @0.3% marginally inferior marginally lotion 0.3% inferior Glycerol ✓ ✓ ✓ ✓ Caprylate @0.5 %in lotion Outperformed Outperformed 0.3% Zero Growth. Outperformed 0 .3 % parabens parabens or 0.4% Equal to 0.3% 0.4%DMDM DMDM Hydantoin parabens or O .4% Hydantoin DMDM Hyclantoin Discussion Additional MIC and Challenge test data will be presented and results and implications discussed. References 1. US Pat 4,002,775 Fatty acids and Derivatives of Antimicrobial Agents, Jon Kabara, (January 11, 1977) 2. A Branan and P Davison, Anti-microbials in Foods, Marcel Dekker, ed., New York, ( 1986) pp 109-140 3. J Kabara, and M Ohkawa, et al., Examination on Antitumor, Immunological, and Plant­ Growth Inhibitory Effects on Monoglycerides of Caprylic Capric and Laurie Acids and Related Compounds Pharmacological Effects of Lipids, Volume II, (1985) pp 263-272

414 JOURNAL OF COSMETIC SCIENCE INORGANIC SUNSCREEN DISPERSIONS: EXPERIENCE WITH DEVELOPMENT AND EVALUATION FOR EFFICACY AND AESTHETICS Art Georgalas1, Elizabeth Kasprzyk1, and Andreas Jung2, Ph.D. 1 TRI-K Industries, Inc, New Paradigm Technologies, Northvale, NJ 2 /FAC GmbH, Duisburg, Germany Formulators must take into consideration multiple factors working with inorganic sunscreens. Because the UV radiation attenuation grade particles of Titanium Dioxide are in the nanometer range, the state of their dispersion in the product film on the skin governs their efficacy and aesthetics.Properties of the particles themselves, including size and coating, the media they are dispersed in and the efficiency and stability of those dispersions impact their performance on the skin. In the final formulation even the same dispersion can give different results depending on the formulation and process. Agglomeration state of particles on the skin film gives variable ratios of UVR and visible light absorption resulting in differences in transparency and sun protection efficacy. Inorganic particles interact with light both optically as inert reflectors and diffractors and as electromagnetic absorbers. They must be effectively dispersed in the finished product and delivered to the skin in a continuous film to work well. An iterative process of experiments using particle size analysis, rheology and suspension properties evaluation to optimize them formulates dispersions. Finally, by looking at in vitro instrumental measurements, in vivo clinical results for efficacy, product draw down films and skin application a full picture of performance emerges.The chronic effects of long-term UVR exposure display as visible signs of aging and increased incidence of some skin cancers. A reproducible bioassay to give immediate assessment of UVR attenuation can only be made with effects that are acute or instrumental methods that simply measure the light flux effects. Acceptable in vivo methods inc1ude sun protection factors (SPF) for UVB radiation generated erythema and the measurement of the effects on persistent pigment darkening (PPD) compared to untreated skin for UVA radiation. In vitro broad-spectrum capability is demonstrated by identification of the critical wavelength of subject product. This is the wavelength at which the area under the absorbance curve beginning at 290 nm up to that wavelength is 90% of the total solar UV radiation absorbed as measured instrumentally from 290- 400 nm, so that, the higher that wavelength the more absorption occurs within the UV A range (320- 400 nm). Additionally, instrumental measurement can estimate a UV A protective factor and a ratio of UV A to DVB attenuation. These are measures accepted or being considered by dermatologists, industry formulators and regulatory agencies worldwide. Premade dispersions of the UVR attenuation pigments make formulation easier but also improve efficacy and aesthetics in some formulations, so that these were under evaluation. Preliminary results with some dispersions indicate more UVB versus UV A attenuation with smaller particles and as less and less agglomerates form. This drives the critical wavelength lower but these formulations still show significant UV A effect along with good sunscreen efficacy by SPF measures. Different grades of titanium dioxide were chosen to represent a full range of varieties available. These included ultra small particle, 10 nm &15 nm, hydrophobically and hydrophilically coated particles, microtitanium dioxide, 35 nm particle size, both uncoated and 20 & 21 nm hydrophilic and hydrophobically coated particles and a larger pigmentary grade of 180 nm plus a new ultra large (1 micron) particle designed to attenuate IR radiation. A variety of Zinc Oxides were also