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Open Access Research article

Solvent effects in permeation assessed in vivo by skin surface biopsy

Catarina Rosado12* and Luis Monteiro Rodrigues1

Author Affiliations

1 Laboratório de Fisiologia Experimental & UCTF – Faculdade de Farmácia da Universidade de Lisboa, Av das Forças Armadas, 1600 Lisboa, Portugal

2 UDE – Unidade de Dermatologia Experimental, Universidade Lusófona, Campo Grande 376, 1700 Lisboa, Portugal

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BMC Dermatology 2003, 3:5  doi:10.1186/1471-5945-3-5

Published: 18 December 2003

Abstract

Background

Transdermal drug delivery has become an important means of drug administration. It presents numerous advantages but it is still limited by the small number of drugs with a suitable profile. The use of solvents that affect the skin barrier function is one of the classic strategies of penetration enhancement. Some of these solvents have well characterised actions on the stratum corneum, but the majority are still selected using empirical criteria. The objective of this work was to conduct a systematic study on the ability to affect skin permeation of solvents commonly used in transdermal formulations. An innovative methodology in this area was employed, consisting of the combination of skin surface biopsy with colorimetry.

Methods

The study compared in vivo differences in the permeation of a hydrophilic (methylene blue) and a lipophilic (Sudan III) dye, after treatment of the skin with different vehicles. Consecutive skin surface biopsies of each site were taken and the cumulative amounts of the dyes in the stripped stratum corneum were measured by reflectance colourimetry.

Results

Results indicate that the amount of methylene blue present in the stratum corneum varied significantly with different skin pre-treatments. Some solvents provided a 1.5 fold penetration enhancement but others decreased by almost half the permeation of the dye. The permeation of Sudan III was less significantly affected by solvent pre-treatment.

Conclusions

This study has only superficially explored the potential of the combination of skin surface biopsy and colourimetry, but the encouraging results obtained confirm that the methodology can be extended to the study of more complex formulations.