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首页> 外文期刊>Materials science & engineering, C. Materials for Biogical applications >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:使用来自三嵌段共聚物MPEG-B-PBAE-B-PLA的pH敏感胶束递送抗癌药物

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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(beta-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) and H-1 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 pH 7.4 to pH 5.0, with over 96% of DOX was released within 48 h. 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:以良好控制的方式改善药物释放速率,一种新的pH敏感三嵌段两亲性共聚物甲基聚(乙二醇)醚-B-聚(β-氨基酯)-B-聚乳酸(MPEG-B-PBAE- B-PLA)及其自组装胶束开发用于抗癌药物递送。通过凝胶渗透色谱法(GPC)和H-1 NMR确认MPEG-B-PBAE-B-PLA的平均分子量和分子结构。通过耗散颗粒动力学(DPD)模拟研究了自组装胶束,不同pH值下的微观结构,以及多柔比蛋白(DOX)的分布,与实验技术相结合。共聚物在水中形成了稳定的核 - 壳型胶束。当PH值从7.4至5.0降低时,坯胶束的临界胶束浓度(CMC)值,颗粒尺寸和Zeta电位随球形延长构象转变而增加,由于PBAE的胺基的质子化。用增加的DOX观察到粒度的明显增加和胶束的药物负载含量。从胶束的DOX的体外释放行为依赖于pH依赖性。 DOX释放率明显改善,因为pH从pH7.4降至pH 5.0,超过96%的DOX在48小时内被释放。还使用理论公式分析了不同条件下的药物释放机制。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的释放行为的抗癌药物输送载体的前瞻性候选。

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