H. Yang, MD, N. Monteiro-Riviere, PhD, H.V. DeBuys, MD, L.C. Walker, Y. Wang, MD, and M. Levine, MD have indicated no significant interest with commercial supporters. S.R. Pinnell, MD is a consultant for Skinceuticals (Dallas, TX). M. Omar, PhD is president of PhytoCeuticals (Elmwood Park, NJ).
Topical L-Ascorbic Acid: Percutaneous Absorption Studies
Article first published online: 7 JUL 2008
DOI: 10.1046/j.1524-4725.2001.00264.x
Additional Information
How to Cite
Pinnell, S. R., Yang, H., Omar, M., Riviere, N. M., DeBuys, H. V., Walker, L. C., Wang, Y. and Levine, M. (2001), Topical L-Ascorbic Acid: Percutaneous Absorption Studies. Dermatologic Surgery, 27: 137–142. doi: 10.1046/j.1524-4725.2001.00264.x
Publication History
- Issue published online: 7 JUL 2008
- Article first published online: 7 JUL 2008
- Abstract
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Background. Reactive oxygen species generated by ultraviolet light result in photocarcinogenic and photoaging changes in the skin. Antioxidants protect skin from these insults.
Objective. This study defines formulation characteristics for delivering L-ascorbic acid into the skin to supplement the skin's natural antioxidant reservoir.
Methods. L-ascorbic acid or its derivatives were applied to pig skin. Skin levels of L-ascorbic acid were measured to determine percutaneous delivery.
Results. L-ascorbic acid must be formulated at pH levels less than 3.5 to enter the skin. Maximal concentration for optimal percutaneous absorption was 20%. Tissue levels were saturated after three daily applications; the half-life of tissue disappearance was about 4 days. Derivatives of ascorbic acid including magnesium ascorbyl phosphate, ascorbyl-6-palmitate, and dehydroascorbic acid did not increase skin levels of L-ascorbic acid.
Conclusions. Delivery of topical L-ascorbic acid into the skin is critically dependent on formulation characteristics.

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