In vivo study of percutaneous absorption of lidocaine using electret in the rat

L. Cui, J. Jiang, C. Song, W. Q. Zhao, D. Weiquan, Z. Xia
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Abstract

The present work was undertaken to study the effect of electret on transdermal drug delivery in vivo. The experiment was carried out in depilated abdominal rat skin using lidocaine hydrochloride as a model compound. Rats were divided into control and electret group. The electrets were applied on the drug in a vial and the blood samples were taken from jugular vein at predetermined time intervals. The concentration of lidocaine in plasma was measured by high proficiency liquid chromatograph (HPLC) after extraction. The plasma lidocaine concentration was significantly increased in electret group. The results suggested that electret could promote the permeability of drug by its effect on the structure of epidermis and blood flow change.
驻极体对大鼠利多卡因经皮吸收的体内研究
本研究旨在研究驻极体对体内经皮给药的影响。实验以盐酸利多卡因为模型化合物,在脱毛的腹部大鼠皮肤上进行。大鼠分为对照组和驻极体组。将驻极体施加在小瓶中的药物上,并在预定的时间间隔内从颈静脉中采集血液样本。提取后用高效液相色谱法测定血浆中利多卡因浓度。驻极体组血浆利多卡因浓度明显升高。结果表明,驻极体通过对表皮结构和血流变化的影响来促进药物的通透性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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