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Poly(l-glutamic acid)-based star-block copolymers as pH-responsive nanocarriers for cationic drugs

机译:基于聚(1-谷氨酸)的星形嵌段共聚物作为阳离子药物的pH响应纳米载体

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摘要

Star-block copolymers PEI-g-(PLG-b-PEG), which consist of a hyperbranched polyethylenimine (PEI) core, a poly(l-glutamic acid) (PLG) inner shell, and a poly(ethylene glycol) (PEG) outer shell, were synthesised and evaluated as nanocarriers for cationic drugs. The synthesised star-block copolymers were characterised by ~1H NMR, gel permeation chromatography (GPC), dynamic light scattering (DLS), and transmission electron microscopy (TEM). Crystal violet (CV), as a model cationic dye, and doxorubicin hydrochloride (DOX), as a model anticancer drug, could be efficiently entrapped by the synthesised star-block copolymers at physiological pH as a result of electrostatic interactions between the cationic guest molecules and the negatively charged PLG segments in the PEI-g-(PLG-b-PEG) host. The drug-polymer complexes showed relatively high temporal stability at physiological pH and sustained release of the encapsulated drugs was observed. The entrapped model compounds demonstrated accelerated release as the pH was gradually decreased.
机译:星型嵌段共聚物PEI-g-(PLG-b-PEG),由高支链聚乙烯亚胺(PEI)核,聚(1-谷氨酸)(PLG)内壳和聚乙二醇(PEG)组成)外壳,并合成为阳离子药物的纳米载体。合成的星形嵌段共聚物通过〜1 H NMR,凝胶渗透色谱法(GPC),动态光散射(DLS)和透射电子显微镜(TEM)进行表征。由于阳离子客体分子之间的静电相互作用,合成的星形嵌段共聚物可以在生理pH下有效地捕获结晶紫(CV)(作为模型阳离子染料)和盐酸阿霉素(DOX)(作为模型抗癌药)。和PEI-g-(PLG-b-PEG)宿主中带负电荷的PLG片段。药物-聚合物复合物在生理pH下显示出相对较高的时间稳定性,并且观察到包封药物的持续释放。截留的模型化合物显示出随着pH值逐渐降低而加速释放。

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