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多尺度研究龙脑对不同 log P 值和分子大小药物透皮渗透的增强作用及机制。

Multiscale study on the enhancing effect and mechanism of borneolum on transdermal permeation of drugs with different log P values and molecular sizes.

机构信息

Beijing University of Chinese Medicine, No. 11 of North 3rd Ring East Road, Chaoyang District, Beijing 100029, China; Key Laboratory for Production Process Control and Quality Evaluation of Traditional Chinese Medicine, Beijing Municipal Science & Technology Commission, Beijing 100029, China.

出版信息

Int J Pharm. 2020 Apr 30;580:119225. doi: 10.1016/j.ijpharm.2020.119225. Epub 2020 Mar 12.

DOI:10.1016/j.ijpharm.2020.119225
PMID:32173500
Abstract

D-borneolum is commonly used as a permeation enhancer in Traditional Chinese Medicine (TCM) formulas for transdermal application. Additionally, two other sources of borneolums were recorded in the 2015 edition of the Chinese Pharmacopoeia (ChP), including L-borneolum and borneolum syntheticum. To guide the selection and application of borneolum, the safety and enhancing effect of three sources of borneolums were investigated on transdermal permeation of compounds with different octanol-water partition coefficient (log P) values and molecular weights (MWs). Both the results of cellular cytotoxicity and in vitro transdermal permeation experiments showed that all three sources of borneolums could be applied in TDDS as permeation enhancers. Moreover, all three sources of borneolums achieved optimal permeation-enhancing performances on transdermal drugs with lower log P values as well as higher MWs. Further study was carried out to elucidate the potential molecular mechanism of borneolum enhancing transdermal drug delivery via transmission electron microscope (TEM) and coarse-grained molecular dynamic (CG-MD) simulation. Borneolum significantly promoted transdermal delivery of drugs via changing the dense morphology of the stratum corneum (SC), disturbing the ordered arrangement of ceramide (CER) and free fatty acid (FFA) molecules in lipid layers, and further increasing the diffusion rate of drugs in the lipid layers.

摘要

龙脑通常被用作中药(TCM)经皮给药配方中的渗透增强剂。此外,在 2015 年版《中国药典》(ChP)中还记录了另外两种龙脑来源,包括左旋龙脑和合成龙脑。为了指导龙脑的选择和应用,研究了三种龙脑来源对不同辛醇-水分配系数(log P)值和分子量(MW)的化合物经皮渗透的安全性和增强作用。细胞毒性和体外经皮渗透实验的结果均表明,三种龙脑来源均可作为经皮给药系统(TDDS)的渗透增强剂。此外,三种龙脑来源在较低 log P 值和较高 MW 的经皮药物中均表现出最佳的渗透增强性能。进一步的研究通过透射电子显微镜(TEM)和粗粒分子动力学(CG-MD)模拟阐明了龙脑增强经皮药物传递的潜在分子机制。龙脑通过改变角质层(SC)的致密形态、扰乱神经酰胺(CER)和游离脂肪酸(FFA)分子在脂质层中的有序排列,进一步增加药物在脂质层中的扩散速率,显著促进了药物的经皮传递。

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