4.6 Review

Transdermal Drug Delivery In Vitro Using Diffusion Cells

Journal

CURRENT MEDICINAL CHEMISTRY
Volume 19, Issue 27, Pages 4671-4677

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/092986712803306358

Keywords

Absorption; dermal; diffusion cell; Franz cell; in vitro; penetration; percutaneous; permeation; skin; transdermal delivery

Funding

  1. Grant of Ministry of Defense of Czech Republic Health Protection against Weapons of Mass Destruction
  2. Internal Grant Agency of Ministry of Health of the Czech Republic [NT12062]

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The assessment of percutaneous absorption of molecules is a very important step in the evaluation of any dermal or transdermal drug delivery system. In order to perform percutaneous drug absorption studies, it is essential that the methods are standardized and that the integrity of the skin is monitored and maintained to ensure that the data obtained are valid and relevant. Reproducible data on percutaneous absorption in humans are as well required to predict the systemic risk from dermal exposure to chemicals, such as hazardous substances at the workplace, agrochemicals and cosmetic ingredients. In vitro and animal models provide important tools for screening a series of drug formulations, evaluation of skin permeation enhancing properties and mechanism of action of the carrier systems and estimation of rank of skin transport for a series of drug molecules. In this review, we have summarized in vitro testing of skin absorption using static Franz-type diffusion cells.

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