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Synthesis and transdermal absorption in vitro of bornyl salicylate / 中国药学杂志
Chinese Pharmaceutical Journal ; (24): 823-826, 2013.
Article in Chinese | WPRIM | ID: wpr-860388
ABSTRACT

OBJECTIVE:

To synthesize bornyl salicylate and study its transdermal absorption in vitro.

METHODS:

Bornyl salicylate was prepared by esterification reaction of (+)-borneol and salicylic acid. The penetration of bornyl salicylate through mouse skin in vitro was measured using Franz diffusing cell with 2% azone as the penetration enhancer. The content of bornyl salicylate was determined by ultraviolet spectrophotometry.

RESULTS:

The structure of the target compound was identified by UV, IR and 1H-NMR. The transdermal absorption of bornyl salicylate was in accordance with Higuchi equation, in which cumulative dose of skin permeation (Q) has a linear relationship with the time. The average cumulative dose of skin permeation of bornyl salicylate for 12 h was 2.6112 mg, and the rate constant was 0.2539 mg m-2-1.

CONCLUSION:

The synthesis method of bornyl salicylate is simple. Bornyl salicylate can penetrate the skin of mice well with 2% azone as the penetration enhancer.

Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Pharmaceutical Journal Year: 2013 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Language: Chinese Journal: Chinese Pharmaceutical Journal Year: 2013 Type: Article