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Synthesis of lipid-based amphiphilic block copolymer and its evaluation as nano drug carrier

机译:脂质基两亲嵌段共聚物的合成及其作为纳米药物载体的评价

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In current study, we report the synthesis and characterization of renewable fatty acid-based block copolymer. The block copolymer was synthesized via RAFT polymerization under microwave irradiations. Firstly, the homo-polymer of N,N-dimethylacrylamide (DMA) was prepared and used as a macro-CTA to copolymerize with modified stearic acid monomer (SAM). The characterization of copolymer p-DMA-b-SAM was done by ~1H NMR, ATR-FT1R and GPC. The block copolymer was allowed to self-assemble and the entrapment of carbamazepine (CBZ) into hydrophobic core of polymeric micelles was investigated in aqueous media. A high drug entrapment efficiency (69%) was observed for block copolymer micelles. The spherical appearance of micelles in the size range of 20-70 nm was determined with transmission electron microscopy (TEM). An effort was also made to investigate the in vitro release profile of CBZ from micelles. A sustained drug release rate was observed, showing complete release of drug within 70 h.
机译:在当前的研究中,我们报告了可再生脂肪酸基嵌段共聚物的合成和表征。在微波辐射下通过RAFT聚合合成嵌段共聚物。首先,制备了N,N-二甲基丙烯酰胺(DMA)的均聚物,并用作大分子CTA与改性硬脂酸单体(SAM)共聚。共聚物p-DMA-b-SAM的表征通过〜1H NMR,ATR-FT1R和GPC进行。使嵌段共聚物自组装,并在水性介质中研究了卡马西平(CBZ)在聚合物胶束疏水核中的包裹。对于嵌段共聚物胶束,观察到高的药物截留效率(69%)。用透射电子显微镜(TEM)测定在20-70nm尺寸范围内的胶束的球形外观。还努力研究了CBZ从胶束的体外释放特性。观察到持续的药物释放速率,显示药物在70小时内完全释放。

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