PMID- 18360561 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20110714 LR - 20211020 IS - 1176-6336 (Print) IS - 1178-203X (Electronic) IS - 1176-6336 (Linking) VI - 1 IP - 3 DP - 2005 Sep TI - Influence of anatomical site and topical formulation on skin penetration of sunscreens. PG - 209-18 AB - Sunscreen products are widely used to protect the skin from sun-related damage. Previous studies have shown that some sunscreen chemicals are absorbed across the skin to the systemic circulation. The current study shows that absorption into the skin of sunscreen chemicals applied to the face is up to four times greater than that of the same product applied to the back. This has implications for the way sunscreen products are formulated and may allow the use of less potent products on the face compared with the rest of the body. The effect of formulation vehicles on the release and skin penetration of the common sunscreen agent benzophenone-3 (common name oxybenzone) was also assessed. Penetration of benzophenone-3 across excised human epidermis and high-density polyethylene (HDPE) membrane was measured using in vitro Franz-type diffusion cells. Penetration and epidermal retention was measured following application of infinite and finite (epidermis only) doses of benzophenone-3 in five vehicles: liquid paraffin, coconut oil, 50:50 ethanol:coconut oil, aqueous cream BP, and oily cream BP. Highest benzophenone-3 skin retention was observed for the ethanol:coconut oil combination. Maximal and minimal benzophenone-3 fluxes were observed from liquid paraffin and coconut oil, respectively. The alcohol-based vehicle exhibited low benzophenone-3 release from the vehicle but high skin penetration and retention. FAU - Benson, Heather Ae AU - Benson HA FAU - Sarveiya, Vikram AU - Sarveiya V FAU - Risk, Stacey AU - Risk S FAU - Roberts, Michael S AU - Roberts MS LA - eng PT - Journal Article PL - New Zealand TA - Ther Clin Risk Manag JT - Therapeutics and clinical risk management JID - 101253281 PMC - PMC1661631 EDAT- 2008/03/25 09:00 MHDA- 2008/03/25 09:01 PMCR- 2006/01/01 CRDT- 2008/03/25 09:00 PHST- 2008/03/25 09:00 [pubmed] PHST- 2008/03/25 09:01 [medline] PHST- 2008/03/25 09:00 [entrez] PHST- 2006/01/01 00:00 [pmc-release] PST - ppublish SO - Ther Clin Risk Manag. 2005 Sep;1(3):209-18.