聚合物囊泡
化学
共聚物
透明质酸
内化
阿霉素
药物输送
纳米载体
纳米颗粒
点击化学
细胞毒性
生物物理学
组合化学
纳米技术
聚合物
材料科学
生物化学
两亲性
细胞
有机化学
体外
外科
化疗
遗传学
生物
医学
作者
K. Kumar Upadhyay,Jean‐François Le Meins,Ambikanandan Misra,Pierre Voisin,Véronique Bouchaud,Emmanuel Ibarboure,Christophe Schatz,Sébastien Lecommandoux
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2009-08-05
卷期号:10 (10): 2802-2808
被引量:203
摘要
Using "click chemistry" as an easy and versatile synthetic strategy to combine hyaluronan and polyglutamate blocks, we have prepared nanovesicles (polymersomes) that present a controlled size, excellent colloidal stability, and a high loading capacity for hydrophilic and hydrophobic drugs. The unique feature of our concept is the use of hyaluronan, a polysaccharide with known capacity for targeting cancer-related protein receptors, as the hydrophilic portion of a block copolymer system. The cytotoxicity and internalization mechanism of doxorubicin-loaded polymersomes have been evaluated in C6 glioma tumor cell lines. The dual purpose served by hyaluronan, as both a hydrophilic block critical to vesicle formation and a binding agent for biological targets, breaks new ground in terms of multifunctional nanomaterial design for drug delivery.
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