Abstract

PurposeThe development of a new two-dimensional (2D) model to predict follicular permeation, with integration into a recently reported multi-scale model of transdermal permeation is presented.MethodsThe follicular pathway is modelled by diffusion in sebum. The mass transfer and partition properties of solutes in lipid, corneocytes, viable dermis, dermis and systemic circulation are calculated as reported previously [Pharm Res 33 (2016) 1602]. The mass transfer and partition properties in sebum are collected from existing literature. None of the model input parameters was fit to the clinical data with which the model prediction is compared.ResultsThe integrated model has been applied to predict the published clinical data of transdermal permeation of caffeine. The relative importance of the follicular pathway is analysed. Good agreement of the model prediction with the clinical data has been obtained. The simulation confirms that for caffeine the follicular route is important; the maximum bioavailable concentration of caffeine in systemic circulation with open hair follicles is predicted to be 20% higher than that when hair follicles are blocked.ConclusionsThe follicular pathway contributes to not only short time fast penetration, but also the overall systemic bioavailability. With such in silico model, useful information can be obtained for caffeine disposition and localised delivery in lipid, corneocytes, viable dermis, dermis and the hair follicle. Such detailed information is difficult to obtain experimentally.

Highlights

  • A major challenge for scientific research regarding skin penetration of drugs, cosmetics, etc., is the development of robust non-animal methods to test percutaneous absorption and bioavailability

  • The aim of this study is to develop a mechanistic model of the follicular pathway and integrate the follicular pathway into our latest multi-scale model of transdermal permeation [19]

  • This paper presents a new in silico model for transdermal permeation and systemic bioavailability with the integration of the follicular pathway

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Summary

Introduction

A major challenge for scientific research regarding skin penetration of drugs, cosmetics, etc., is the development of robust non-animal methods to test percutaneous absorption and bioavailability. There is a general trend in safety regulatory guidelines worldwide to move away from animal testing of cosmetic products and ingredients (e.g. the European Commission) [3]. In parallel to the advancement in experimental methods, in silico modelling of dermal absorption and delivery has been demonstrated to be useful in refining and reducing the experiments needed, to enable faster design of new products and more reliable safety assessment, and to improve the understanding of the transport process [2]. In silico modelling has become an important tool in the study of topical and transdermal delivery

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