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生物可降解两亲性嵌段共聚物胶束的制备及其对叶酸的控制释放 被引量:1

Preparation of amphiphilic biodegradable block copolymer micelle and its controlled release on folic acid
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摘要 以甲氧基聚乙二醇(mPEG)为引发剂,在辛酸亚锡催化下引发ε-环己内酯(CL)开环聚合,合成了聚乙二醇-聚己内酯两亲性嵌段共聚物(mPEG-PCL)。通过FTIR、1H-NMR及GPC等表征手段确定了mPEG-PCL的组成及结构。采用芘荧光探针法、透射电镜和动态激光光散射研究了聚合物在水中的自组装行为。结果表明:聚合物在水溶液中能够自组装形成粒径小于100 nm的规则球状胶束,且具有较低的临界胶束浓度(7.35×10-3 g/L);模型药物(叶酸)成功负载于聚合物纳米胶束内,并且能延缓叶酸的释放,其释药速率受载药量和释放介质pH的影响。 Amphiphilic block copolymer mPEG-b-PCL was synthesized by the ring-opening polymerization of e-caprolactone(e-CL) employing SnOch as catalyst and methoxypoly(ethylene glycol) (mPEG) as macro-initiator. The structure and molecular weight were characterized by FT-IR, IH-NMR and GPC. The self-assembled behavior in water was studied by pyrene fluorescence probe technique, transmission electron microscopy(TEM) and dynamic laser light scattering(DLS). The results show that mPEG-b-PCL could self-assemble to form micelle with a low CMC (7.35× 10^-3 g/L), nano-size (〈100 nm) and regularly spherical in shape in aqueous solution. Model drug folic acid(FA) was incorporated into the micelles, the in vitro drug release characteristics suggested that the drug-loaded micelles could sustain the drug release, and the drug release rate were affected by the drug loading content and the pH of the release media.
出处 《胶体与聚合物》 2010年第3期99-102,共4页 Chinese Journal of Colloid & Polymer
基金 国家自然科学基金(50273010) 河南大学科研基金(072R2D010)
关键词 两亲性嵌段共聚物 聚合物胶束 药物载体 控制释放 Amphiphilic Block Copolymer Polymer Micelle Drug Carrier Controlled Release
作者简介 刘学军(1976-),男,硕士,主要从事功能高分子及生物医用高分子研究。E—mail:liuxuejun@henu.edu.cn. 通讯作者:高青雨教授,E—mail:qyg515@126.com.
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共引文献22

同被引文献17

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