Recent advances in the brain targeting of neuropharmaceuticals by chemical delivery systems

被引:139
作者
Bodor, N [1 ]
Buchwald, P [1 ]
机构
[1] Univ Florida, Hlth Sci Ctr, Ctr Drug Discovery, Gainesville, FL 32610 USA
关键词
blood-brain barrier; brain-targeted redox analog; cyclodextrin; estradiol; neuropeptides; octanol-water; partition; P-glycoprotein; retrometabolic design; zidovudine (AZT);
D O I
10.1016/S0169-409X(98)00090-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Brain-targeted chemical delivery systems represent a general and systematic method that can provide localized and sustained release for a variety of therapeutic agents including neuropeptides. By using a sequential metabolism approach, they exploit the specific trafficking properties of the blood-brain barrier and provide site-specific or site-enhanced delivery. After a brief description of the design principles, the present article reviews a number of specific delivery examples (zidovudine, ganciclovir, lomustine benzylpenicillin, estradiol, enkephalin, TRH, kyotorphin), together with representative synthetic routes, physicochemical properties, metabolic pathways, and pharmacological data. A reevaluated correlation for more than 60 drugs between previously published in vivo cerebrovascular permeability data and octanol/water partition coefficients is also included since it may be useful in characterizing the properties of the blood-brain barrier, including active transport by P-glycoprotein. (C) 1999 Elsevier Science BN. All rights reserved.
引用
收藏
页码:229 / 254
页数:26
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