Title of article :
Synthesis and transdermal permeation-enhancing activity of ketone, amide, and alkane analogs of Transkarbam 12 Original Research Article
Author/Authors :
Tom?? Holas، نويسنده , , Kate?ina V?vrov?، نويسنده , , Jana Klimentov?، نويسنده , , Alexandr Hrab?lek، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2006
Pages :
8
From page :
2896
To page :
2903
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.
Keywords :
Structure–activity relationships , Hydrogen bonding , Transdermal drug delivery , Percutaneous absorption , Carbamate , Permeation enhancer
Journal title :
Bioorganic and Medicinal Chemistry
Serial Year :
2006
Journal title :
Bioorganic and Medicinal Chemistry
Record number :
1305660
Link To Document :
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