Can models of percutaneous absorption based on in vitro data in frogs predict in vivo absorption?


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 14 08 2019
accepted: 23 06 2020
entrez: 30 7 2020
pubmed: 30 7 2020
medline: 12 9 2020
Statut: epublish

Résumé

The primary aim of in vitro testing of chemicals delivered via the percutaneous route is to predict the absorption that would ensue if exposure occurred in live animals. While there is mounting evidence that in vitro diffusion studies in mammalian skin can provide valid information regarding likely in vivo absorption, little is known whether such a correlation exists between in vitro diffusion testing and in vivo blood levels in amphibians. The current study used previously-reported in vitro absorption data for caffeine, benzoic acid, and ibuprofen across isolated skin from the cane toad (Rhinella marina) to produce a series of linear mixed-effect models of the absorption parameters flux and permeability coefficient (Kp). Models investigated the relative impacts of animal weight, physicochemical characteristics of the applied chemical (logP or molecular weight), and site of application. The top models were then used to predict the flux, Kp and serum concentrations of the same three model chemicals. Finally, the absorption of these chemicals was determined in live cane toads, and results compared to the model predictions. LogP and site of application were included in all top models. In vivo absorption rates were lower than predicted for all chemicals, however, the models provided reasonable predictions of serum concentration, with factors of difference (FOD) ranging from 2.5-10.5. Ibuprofen, the chemical with the highest relative lipophilicity, had the poorest predictive performance, consistently having the highest FOD for all predictions. This report presents the first models of percutaneous absorption in an amphibian. These models provide a basic method to establish the approximate in vivo absorption of hydrophilic and moderately-lipophilic chemicals through frog skin, and could therefore be used to predict absorption when formulating such chemicals for treatment of disease in frogs, or for risk-assessments regarding chemical pollutants in frog habitats.

Identifiants

pubmed: 32726322
doi: 10.1371/journal.pone.0235737
pii: PONE-D-19-23024
pmc: PMC7390353
doi:

Substances chimiques

Caffeine 3G6A5W338E
Benzoic Acid 8SKN0B0MIM
Ibuprofen WK2XYI10QM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0235737

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Références

Skin Pharmacol Appl Skin Physiol. 2003 Nov-Dec;16(6):343-55
pubmed: 14528058
Skin Pharmacol Physiol. 2011;24(4):224-30
pubmed: 21455015
Med Mycol. 2019 Feb 1;57(2):204-214
pubmed: 29566178
Comp Biochem Physiol. 1965 Jun;15(2):81-8
pubmed: 5841615
Environ Toxicol Pharmacol. 2008 May;25(3):373-9
pubmed: 21783876
Hum Exp Toxicol. 2008 Apr;27(4):281-8
pubmed: 18684798
Environ Toxicol Chem. 2019 Feb;38(2):361-367
pubmed: 30370675
Adv Drug Deliv Rev. 2007 Sep 30;59(11):1152-61
pubmed: 17889400
J Invest Dermatol. 1975 Mar;64(3):190-5
pubmed: 123263
PLoS One. 2009 Nov 04;4(11):e7699
pubmed: 19888346
Environ Sci Eur. 2016;28(1):10
pubmed: 27752445
J Vet Pharmacol Ther. 2016 Apr;39(2):109-21
pubmed: 26456710
EFSA J. 2018 Feb 23;16(2):e05125
pubmed: 32625798
Comp Biochem Physiol C Pharmacol Toxicol Endocrinol. 1998 Nov;121(1-3):85-105
pubmed: 9972453
J Pharm Sci. 2007 Apr;96(4):824-34
pubmed: 17177207
Environ Toxicol Pharmacol. 2018 Jun;60:5-11
pubmed: 29631153
Heliyon. 2019 Aug 16;5(8):e02127
pubmed: 31463380
J Physiol. 1976 Oct;261(3):603-15
pubmed: 824445
J Chromatogr. 1981 Nov 13;226(1):183-90
pubmed: 7320142
Environ Toxicol Pharmacol. 2006 Nov;22(3):255-62
pubmed: 21783718

Auteurs

Victoria K Llewelyn (VK)

Pharmacy, College of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.

Lee Berger (L)

One Health Research Group, Melbourne Veterinary School, University of Melbourne, Werribee, Victoria, Australia.

Beverley D Glass (BD)

Pharmacy, College of Medicine and Dentistry, James Cook University, Townsville, Queensland, Australia.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH