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Development of a robust pH-sensitive polyelectrolyte ionomer complex for anticancer nanocarriers

机译:用于抗癌纳米载体的强健的pH敏感型聚电解质离聚物复合物的开发

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摘要

A polyelectrolyte ionomer complex (PIC) composed of cationic and anionic polymers was developed for nanomedical applications. Here, a poly(ethylene glycol)–poly(lactic acid)–poly(ethylene imine) triblock copolymer (PEG–PLA–PEI) and a poly(aspartic acid) (P[Asp]) homopolymer were synthesized. These polyelectrolytes formed stable aggregates through electrostatic interactions between the cationic PEI and the anionic P(Asp) blocks. In particular, the addition of a hydrophobic PLA and a hydrophilic PEG to triblock copolyelectrolytes provided colloidal aggregation stability by forming a tight hydrophobic core and steric hindrance on the surface of PIC, respectively. The PIC showed different particle sizes and zeta potentials depending on the ratio of cationic PEI and anionic P(Asp) blocks (C/A ratio). The doxorubicin (dox)-loaded PIC, prepared with a C/A ratio of 8, demonstrated pH-dependent behavior by the deprotonation/protonation of polyelectrolyte blocks. The drug release and the cytotoxicity of the dox-loaded PIC (C/A ratio: 8) increased under acidic conditions compared with physiological pH, due to the destabilization of the formation of the electrostatic core. In vivo animal imaging revealed that the prepared PIC accumulated at the targeted tumor site for 24 hours. Therefore, the prepared pH-sensitive PIC could have considerable potential as a nanomedicinal platform for anticancer therapy.
机译:由阳离子和阴离子聚合物组成的聚电解质离聚物配合物(PIC)已开发用于纳米医学应用。在这里,合成了聚(乙二醇)-聚(乳酸)-聚(乙烯亚胺)三嵌段共聚物(PEG-PLA-PEI)和聚(天冬氨酸)(P [Asp])均聚物。这些聚电解质通过阳离子PEI和阴离子P(Asp)嵌段之间的静电相互作用形成稳定的聚集体。特别地,向三嵌段共聚电解质中添加疏水性PLA和亲水性PEG通过分别在PIC表面上形成紧密的疏水性核和位阻,从而提供了胶体聚集稳定性。 PIC显示出不同的粒径和Zeta电位,具体取决于阳离子PEI和阴离子P(Asp)嵌段的比例(C / A比)。以8的C / A比率制备的负载阿霉素(dox)的PIC通过聚电解质嵌段的去质子化/质子化显示了pH依赖的行为。与酸性pH相比,由于静电核心形成的不稳定,在酸性条件下,载有dox的PIC的药物释放和细胞毒性(C / A比:8)增加。体内动物成像显示,制备的PIC在目标肿瘤部位累积了24小时。因此,所制备的pH敏感型PIC可以作为抗癌治疗的纳米药物平台具有巨大的潜力。

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