The effect of dendrimers on the pharmacodynamic and pharmacokinetic behaviors of non-covalently or covalently attached drugs

被引:108
作者
Cheng, Yiyun [1 ,2 ,3 ]
Xu, Tongwen [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Lab Funct Membranes, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Hefei Natl Lab Phys Sci Microscale, Hefei 230027, Anhui, Peoples R China
[3] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
关键词
Dendrimer; Pharmacodynamic; Pharmacokinetic; Complex; Conjugate; Drug delivery system;
D O I
10.1016/j.ejmech.2007.12.021
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Dendrimers are a new class of artificial macromolecules with several attractive properties that show promises in several biomedical applications. They can be widely used to increase the cellular uptake, bioavailability and therapeutic efficacy, to optimize the biodistribution and intracellular release profile, and to reduce the systemic toxicity, clearance and degradation rate of non-covalently or covalently attached drugs. Recent studies in this aspect clearly point to the potential advantages of dendrimers for the design of new drug delivery systems. Before final applications of dendrimer-based drug delivery systems in humans, we should not only address the benefits of these systems, but also assess the long-term pharmacodynamic (PD) and pharmacokinetic (PK) behaviors and health risk of them. In this mini-review, we will mainly discuss the influence of dendrimers on the PD and PK behaviors of drugs complexed or conjugated to them. (C) 2008 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:2291 / 2297
页数:7
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