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pH-responsive polymeric micelles with core–shell–corona architectures as intracellular anti-cancer drug carriers

机译:具有核-壳-电晕结构的pH响应聚合物胶束作为细胞内抗癌药物载体

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Polymeric micelles with core–shell–corona nanoarchitecture were designed for intracellular therapeutic anti-cancer drug carriers. Poly(styrene-b-acrylic acid-b-ethylene glycol) (PS-b-PAA-b-PEG) asymmetric triblock copolymer underwent self-assembly in aqueous solution to form spherical micelles with hydrophobic PS core, anionic PAA shell and hydrophilic PEG corona. The anti-cancer drug (doxorubicin, DOX) was successfully incorporated into the polymeric micelles. The in vitro release experiment confirmed that the release of DOX from the micelles was inhibited at pH 7.4. In contrast, an accelerated release of DOX was observed at mildly acidic conditions such as pH 4.5. The excellent biocompatibility of our PS-b-PAA-b-PEG-based micelles made the synthesized nano-carrier best suited for the delivery of anti-cancer drugs.
机译:具有核-壳-电晕纳米结构的聚合物胶束设计用于细胞内治疗性抗癌药物载体。聚(苯乙烯-b-丙烯酸-b-乙二醇)(PS-b-PAA-b-PEG)不对称三嵌段共聚物在水溶液中自组装形成具有疏水PS核,阴离子PAA壳和亲水PEG的球形胶束电晕。将抗癌药(阿霉素,DOX)成功地掺入了聚合物胶束中。体外释放实验证实,在pH 7.4下,胶束中DOX的释放受到抑制。相反,在中等酸性条件下(例如pH 4.5)观察到DOX加速释放。我们的基于PS-b-PAA-b-PEG的胶束具有出色的生物相容性,使合成的纳米载体最适合用于抗癌药物的输送。

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