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首页> 外文期刊>Materials science & engineering >Delivery of anticancer drug using pH-sensitive micelles from triblock copolymer MPEG-b-PBAE-b-PLA
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Delivery of anticancer drug using pH-sensitive micelles from triblock copolymer MPEG-b-PBAE-b-PLA

机译:使用pH敏感胶束从三嵌段共聚物MPEG-b-PBAE-b-PLA递送抗癌药物

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To improve the drug release rate in well-controlled manner, a new pH-sensitive triblock amphiphilic copolymer methyl poly(ethylene glycol) ether-b-poly(β-amino esters)-b-poly lactic acid (MPEG-b-PBAE-b-PLA) and its self-assembled micelles were developed for anticancer drug delivery. The average molecular weight and molecular structure of MPEG-b-PBAE-b-PLA were confirmed by gel permeation chromatography (GPC) and1H NMR. The formation of self-assembled micelles, the microstructures at different pH values, and the distribution of doxorubicin (DOX) were investigated by dissipative particle dynamics (DPD) simulation combined with experimental techniques. The copolymers formed stable core-shell-type micelles in water. The critical micelle concentration (CMC) values, particle sizes and zeta potentials of the blank micelles increased along with globule-extended conformational transitions when the pH values decreased from 7.4 to 5.0, due to the protonation of amine groups of PBAE. Obvious increases in the particle sizes and the drug loading content of micelles were observed with increasing DOX. The in vitro release behavior of DOX from the micelles was pH-dependent. The DOX release rate was improved obviously as pH decreased from pH7.4 to pH5.0, with over 96% of DOX was released within 48h. The drug release mechanism under different conditions was also analyzed using theoretical formulas. All the results suggest that the pH-sensitive MPEG-b-PBAE-b-PLA micelles might be a prospective candidate as anticancer drug delivery carrier with well-controlled release behavior.
机译:为了以可控的方式提高药物释放速率,一种新型的pH敏感型三嵌段两亲共聚物甲基聚乙二醇醚-b-聚(β-氨基酯)-b-聚乳酸(MPEG-b-PBAE-开发了b-PLA)及其自组装的胶束用于抗癌药物的递送。 MPEG-b-PBAE-b-PLA的平均分子量和分子结构通过凝胶渗透色谱法(GPC)和1 H NMR确证。通过耗散粒子动力学(DPD)模拟结合实验技术,研究了自组装胶束的形成,不同pH值下的微结构和阿霉素(DOX)的分布。共聚物在水中形成稳定的核-壳型胶束。当PBAE的胺基质子化使pH值从7.4降低到5.0时,空白胶束的临界胶束浓度(CMC)值,粒径和zeta电位随着小球延伸的构象转变而增加。随着DOX的增加,胶束的粒径和载药量明显增加。 DOX从胶束的体外释放行为是pH依赖性的。当pH从pH7.4降至pH5.0时,DOX释放速率明显提高,在48小时内释放出96%以上的DOX。还使用理论公式分析了不同条件下的药物释放机理。所有结果表明,pH敏感的MPEG-b-PBAE-b-PLA胶束可能是具有良好控制释放行为的抗癌药物输送载体。

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