Vehicle influence on permeation through intact and compromised skin

Int J Pharm. 2014 Sep 10;472(1-2):362-8. doi: 10.1016/j.ijpharm.2014.06.050. Epub 2014 Jun 27.

Abstract

The purpose of this study was to compare the transdermal permeation of a model compound, diclofenac diethylamine, from a hydrophilic and lipophilic vehicle across in vitro models simulating compromised skin. Mineral oil served as a lipophilic vehicle while 10mM phosphate buffered saline served as a hydrophilic vehicle. Compromised skin was simulated by tape stripping, delipidization, or microneedle application and compared with intact skin as a control. Transepidermal water loss was measured to assess barrier function. Skin compromised with tape stripping and delipidization significantly (p<0.05) increased permeation of diclofenac diethylamine compared to intact and microneedle treated skin with phosphate buffered saline vehicle. A similar trend in permeation was observed with mineral oil as the vehicle. For both vehicles, permeation across skin increased in the same order and correlated with degree of barrier impairment as indicated by transepidermal water loss values: intact<microneedles<tape stripping<delipidization. A study with hairless rats comparing both vehicles found the same trend, with hydrophilic vehicle having greater delivery. In conclusion, phosphate buffered saline vehicle resulted in higher permeation into and across skin compared to mineral oil vehicle for all simulated models of compromised skin.

Keywords: Compromised skin; Diclofenac; Percutaneous; Transdermal; Vehicle.

MeSH terms

  • Administration, Topical
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacokinetics
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Diclofenac / chemistry
  • Diclofenac / pharmacokinetics
  • Diclofenac / pharmacology*
  • Humans
  • Hydrophobic and Hydrophilic Interactions
  • In Vitro Techniques
  • Male
  • Mineral Oil / chemistry
  • Mineral Oil / pharmacology*
  • Permeability / drug effects
  • Pharmaceutical Vehicles / chemistry
  • Pharmaceutical Vehicles / pharmacology*
  • Rats, Hairless
  • Skin / drug effects
  • Skin / injuries
  • Skin / metabolism
  • Skin Absorption / drug effects*
  • Sodium Chloride / chemistry
  • Sodium Chloride / pharmacology*
  • Solubility
  • Water / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Pharmaceutical Vehicles
  • Water
  • Diclofenac
  • Sodium Chloride
  • Mineral Oil