Synthesis and transdermal permeation-enhancing activity of ketone, amide, and alkane analogs of Transkarbam 12

Bioorg Med Chem. 2006 May 1;14(9):2896-903. doi: 10.1016/j.bmc.2005.12.006. Epub 2006 Jan 11.

Abstract

Transkarbam 12 (5-(dodecyloxycarbonyl)pentylammonium-5-(dodecyloxycarbonyl)pentylcarbamate, T12) is a highly active transdermal permeation enhancer. In this study, ketone, amide, and alkane analogs of T12 have been synthesized and evaluated for their permeation-enhancing activity using porcine skin and theophylline as a model drug. Replacement of ester by methylene and ketone, respectively, led to a significant decrease of activity. Amide analogs displayed lower activity in 60% propylene glycol and were comparable to T12 in isopropyl myristate. An intramolecular H-bond between ester and ammonium-carbamate group was suggested to be important for the permeation-enhancing activity of T12.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adjuvants, Pharmaceutic / chemical synthesis*
  • Adjuvants, Pharmaceutic / chemistry
  • Adjuvants, Pharmaceutic / pharmacology*
  • Alkanes / chemistry*
  • Amides / chemistry*
  • Animals
  • Carbamates / chemical synthesis
  • Carbamates / chemistry*
  • Carbamates / pharmacology*
  • Ketones / chemistry*
  • Models, Molecular
  • Skin Absorption / drug effects
  • Structure-Activity Relationship
  • Swine
  • Theophylline / pharmacology

Substances

  • Adjuvants, Pharmaceutic
  • Alkanes
  • Amides
  • Carbamates
  • Ketones
  • transkarbam 12
  • Theophylline