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Pakistan Journal of Pharmaceutical Sciences. 2011; 24 (4): 451-457
in English | IMEMR | ID: emr-137543

ABSTRACT

In the present study a new alcohol derivative of tetrahydrogeraniol [THG], an acyclic monoterpene, has been prepared by using Grignard reagent and methyl cyclopropyl ketone. Penetration enhancing effects of THG and the synthesized derivative 5,9-dimethyl-2-cyclopropyl-2-decanol [DICNOL] on the transdermal penetration of 5-fluorouracil [5-FU] and tramadol hydrochloride [tramadol HC1] across the excised rat skin were studied by an in vitro permeation technique using Franz diffusion cells. Azone was used as standard enhancer for comparison. DICNOL and THG significantly enhanced 5-FU and tramadol HC1 penetration through rat skin compared with the control. DICNOL enhanced the permeability of 5-FU and tramadol HC1 across full thickness skin by about 11 and 20 fold, respectively. Increased partition coefficient and diffusion coefficient values were obtained by these enhancers. The results suggest that the amount of DICNOL in the skin, especially in the stratum corneum, may be related to its penetration enhancing effects


Subject(s)
Animals, Laboratory , Male , Fatty Alcohols/pharmacokinetics , Fatty Alcohols/chemical synthesis , Skin Absorption/drug effects , Terpenes/chemistry , Adjuvants, Pharmaceutic , Terpenes/pharmacology , Rats, Sprague-Dawley , Skin/drug effects , Skin/metabolism , Evaluation Studies as Topic , Molecular Structure , Permeability/drug effects , Pharmaceutical Preparations , Tramadol/metabolism
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