Penetration of Ammonium Perfluorooctanoate Through Rat and Human Skin In Vitro
Autor: | B. Szostek, Gerald L. Kennedy, L. Haroun, D. G. Farrar, R. J. Ward, Paul M. Hinderliter, William J. Fasano |
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Rok vydání: | 2005 |
Předmět: |
Skin Absorption
Health Toxicology and Mutagenesis Kinetics Human skin Absorption (skin) In Vitro Techniques Toxicology Permeability Rats Sprague-Dawley Animals Humans Toxicokinetics Pharmacology Fluorocarbons Chemical Health and Safety Chromatography Aqueous solution integumentary system Parafilm Chemistry Public Health Environmental and Occupational Health General Medicine Penetration (firestop) Rats Membrane Caprylates Epidermis |
Zdroj: | Drug and Chemical Toxicology. 28:79-90 |
ISSN: | 1525-6014 0148-0545 |
DOI: | 10.1081/dct-39707 |
Popis: | Rat and human epidermal membranes were mounted onto in vitro diffusion cells with an exposure area of 0.64 cm2, and skin integrity was confirmed using electrical impedance. Following membrane selection, Fluorad FC-118, a 20% aqueous solution of ammonium perfluorooctanoate (AFPO), was applied to the epidermal surface of each skin replicate at approximately 150 microL/cm2 and the donor chamber opening occluded with Parafilm. Serial receptor fluid samples were collected hourly from 1 to 6 h and at 12, 24, 30, and 48 h and analyzed by liquid chromatography-mass spectrometry (LC-MS) for APFO anion (PFO-). For rat skin, the time to steady-state penetration (6500+/-3000 ng APFO x cm(-2) x h(-1)) occurred in less than 12 h, which was sustained until termination (48 h). Based on the concentration of the applied test material, the permeability coefficient (Kp) for APFO in rat skin was calculated to be 3.25+/-1.51 x 10(-5) cm/h. By end of the 48-h exposure period, only a small portion of the total APFO applied (1.44+/-1.13%) had penetrated through rat skin. For human skin, steady-state penetration of APFO (190+/-57 ng APFO x cm(-2) x h(-1)) was reached by 12 h. Based on the concentration of the applied test material, the permeability coefficient for APFO in human skin was calculated to be 9.49+/-2.86 x 10(-7) cm/h. By the end of the 48-h exposure period, only a negligible amount of the total APFO applied (0.048+/-0.01%) had penetrated through human skin. Thus, under infinite dose and occlusive conditions, the steady-state penetration of APFO from a 20% solution was approximately 34-fold faster through rat skin than human skin. |
Databáze: | OpenAIRE |
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