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磷脂膜色谱及其在药物跨膜转运评价中的应用
引用本文:孙进,张天虹,何仲贵. 磷脂膜色谱及其在药物跨膜转运评价中的应用[J]. 色谱, 2005, 23(4): 378-383
作者姓名:孙进  张天虹  何仲贵
作者单位:Department of Biopharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
基金项目:国家自然科学基金资助项目(No.30400563).
摘    要:磷脂膜色谱是固态基质上的有序磷脂分子单层体系采用色谱学方法仿真药物与细胞膜相互作用过程,可用来评价药物的细胞膜渗透性和活性。硅胶表面上的磷脂单分子层模拟了单层细胞膜,因此药物的磷脂膜色谱保留行为可用于预测药物与细胞膜的相互作用。目前考察药物跨膜转运的模型主要有正辛醇/水系统、脂质体/水系统、反相色谱(ODS)以及磷脂膜色谱。与前述3种系统比较,磷脂膜色谱除了具有高效、简便等特点外,同时能模拟药物与生物膜之间疏水作用力以外的其他作用力,因此对磷脂膜色谱的研究也越来越深入。由于药物细胞膜渗透性对其有效性和安全性起着关键作用,因此磷脂膜色谱在新药研发早期阶段的介入可以有效地降低后期候选药物的淘汰率,提高新药的研发效率。该文就磷脂膜色谱的研究及在药物跨膜转运评价中的应用进行了综述。

关 键 词:跨膜转运  磷脂膜色谱  膜作用  综述  
文章编号:1000-8713(2005)04-0378-06
收稿时间:2004-09-07
修稿时间:2004-09-07

Immobilized Artificial Membrane Chromatography and Its Application in Profiling the Drug Membrane Transport
SUN Jin,Zhang Tianhong,HE Zhonggui. Immobilized Artificial Membrane Chromatography and Its Application in Profiling the Drug Membrane Transport[J]. Chinese journal of chromatography, 2005, 23(4): 378-383
Authors:SUN Jin  Zhang Tianhong  HE Zhonggui
Affiliation:Department of Biopharmaceutics, School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China
Abstract:Immobilized artificial membrane chromatography (IAMC) is a system of covalently bonding monolayer of phospholipid analogs onto the solid surface of silica particles, thus establishing the emulating process of drug-cellular membrane interactions in terms of chromatographic method, and is applied to profile the drug membrane permeability and biological activity. IAMC phases prepared from phosphocholine analogues closely mimic the surface of the biological cell membrane, and the capacity factor of drugs can be used to predict the interaction (between) drug molecules and cell membranes. IAMC, compared with n-octanol/water, liposome/water and ODS chromatography, can simulate other forces besides hydrophobic interaction. IAMC is getting more and more profound research because of its convenience and high (efficiency.) The primary screening by means of IAMC in the early stage of drug development would effectively lower failure in the preclinical and clinical development, since efficacy and safety are related in the larger part to membrane permeability. The interaction mechanism of drug-IAM and its profiling in membrane transport are reviewed.
Keywords:immobilized artificial membrane chromatography  membrane interactions  membrane transport  review
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