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Self-Assembled Polymeric Micellar Nanoparticles as Nanocarriers for Poorly Soluble Anticancer Drug Ethaselen

机译:自组装的聚合物胶束纳米颗粒作为难溶性抗癌药物乙烷的纳米载体

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摘要

A series of monomethoxy poly(ethylene glycol)-poly(lactide) (mPEG-PLA) diblock copolymers were synthesized, and mPEG-PLA micelle was fabricated and used as a nanocarrier for solubilization and delivery of a promising anticancer drug ethaselen. Ethaselen was efficiently encapsulated into the micelles by the dialysis method, and the solubility of ethaselen in water was remarkably increased up to 82 μg/mL before freeze-drying. The mean diameter of ethaselen-loaded micelles ranged from 51 to 98 nm with a narrow size distribution and depended on the length of PLA block. In vitro hemolysis study indicated that mPEG-PLA copolymers and ethaselen-loaded polymeric micelles had no hemolytic effect on the erythrocyte. The enhanced antitumor efficacy and reduced toxic effect of ethaselen-loaded polymeric micelle when compared with ethaselen-HP-β-CD inclusion were observed at the same dose in H22human liver cancer cell bearing mouse models. These suggested that mPEG-PLA polymeric micelle nanoparticles had great potential as nanocarriers for effective solubilization of poorly soluble ethaselen and further reducing side effects and toxicities of the drug.
机译:合成了一系列单甲氧基聚(乙二醇)-聚(丙交酯)(mPEG-PLA)二嵌段共聚物,并制备了mPEG-PLA胶束并将其用作纳米载体,用于增溶和递送有前途的抗癌药物乙基纤维素。通过透析方法将乙基纤维素有效地包封在胶束中,并在冻干之前将乙基纤维素在水中的溶解度显着提高至82μg/ mL。负载有乙基纤维素的胶束的平均直径范围为51至98 nm,尺寸分布较窄,并取决于PLA嵌段的长度。体外溶血研究表明,mPEG-PLA共聚物和负载乙二胺的聚合物胶束对红细胞没有溶血作用。在荷人肝癌细胞H22小鼠模型中,在相同剂量下观察到与负载乙二胺酯-HP-β-CD包合物相比,乙二胺酯负载的聚合物胶束的增强的抗肿瘤功效和降低的毒性作用。这些表明,mPEG-PLA聚合物胶束纳米颗粒具有作为纳米载体的巨大潜力,可有效溶解难溶的乙二胺,并进一步降低药物的副作用和毒性。

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