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用于药物递送的二嵌段共聚物纳米颗粒。

Diblock copolymer nanoparticles for drug delivery.

作者信息

Kwon G S

机构信息

School of Pharmacy, University of Wisconsin at Madison 53706-1508, USA.

出版信息

Crit Rev Ther Drug Carrier Syst. 1998;15(5):481-512.

PMID:9822868
Abstract

Diblock copolymers can form nanoparticles, that is, micelles and nanospheres, that are being studied as carriers for hydrophobic drugs and genes. The synthetic carriers mimic the spherical, supramolecular core/shell structure of lipoproteins and viruses. Hence, diblock copolymer nanoparticles may be functional, having the ability to solubilize, protect, and release drugs at sustained rates. Several studies have illustrated prolonged residence times in blood for diblock copolymer nanoparticles. They have also enhanced drug effects in animals. Diblock copolymer nanoparticles are potentially useful carriers for site-specific drug delivery.

摘要

二嵌段共聚物可以形成纳米颗粒,即胶束和纳米球,它们正作为疏水性药物和基因的载体进行研究。合成载体模仿脂蛋白和病毒的球形超分子核/壳结构。因此,二嵌段共聚物纳米颗粒可能具有功能性,具备以持续速率溶解、保护和释放药物的能力。多项研究表明二嵌段共聚物纳米颗粒在血液中的停留时间延长。它们还增强了在动物体内的药物效果。二嵌段共聚物纳米颗粒是用于定点给药的潜在有用载体。

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