Dicarboxylic acid esters as transdermal permeation enhancers: effects of chain number and geometric isomers

Bioorg Med Chem Lett. 2009 Jan 15;19(2):344-7. doi: 10.1016/j.bmcl.2008.11.083. Epub 2008 Nov 27.

Abstract

A series of transdermal permeation enhancers based on dicarboxylic acid esters was studied. Single-chain amphiphiles were markedly more effective than the double-chain ones. Monododecyl maleate, that is a cis derivative, was a more potent enhancer than its trans isomer, while the activity of succinates strongly depended on the donor vehicle. No difference between diastereoisomeric tartaric and meso-tartaric acid derivatives was found.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dicarboxylic Acids / chemistry
  • Dicarboxylic Acids / pharmacology*
  • Esters
  • Isomerism
  • Skin Absorption / drug effects*

Substances

  • Dicarboxylic Acids
  • Esters