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Self-Assembled Nanoparticles Based on PEGylated Conjugated Polyelectrolyte and Drug Molecules for Image-Guided Drug Delivery and Photodynamic Therapy

机译:基于聚乙二醇化共轭聚电解质和药物分子的自组装纳米颗粒,用于图像引导的药物递送和光动力疗法

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A drug delivery system based on poly(ethylene glycol) (PEG) grafted conjugated polyelectrolyte (CPE) has been developed to serve as a polymeric photosensitizer and drug carrier for combined photodynamic and chemotherapy. The amphiphilic brush copolymer can self-assemble into micellar nanopaticles (NPs) in aqueous media with hydrophobic conjugated polyelectrolyte backbone as the core and hydrophilic PEG as the shell. The NPs have an average diameter of about 100 nm, with the absorption and emission maxima at 502 and 598 nm, respectively, making them suitable for bioimaging applications. Moreover, the CPE itself can serve as a photosensitizer, which makes the NPs not only a carrier for drug but also a photosensitizing unit for photodynamic therapy, resulting in tine combination of chemo- and photodynamic therapy for cancer. The half-maximal inhibitory concentration (IC_(50)) value for the combination therapy to U87-MG cells is 12.7 μg mL~(-1), which is much lower than that for the solely photodynamic therapy (25.5 μg mL~(-1)) or chemotherapy (132.8 μg mL~(-1)). To improve the tumor specificity of the system, cyclic arginine-glycine-aspartic acid (cRGD) tripeptide as the receptor to integrin α_vβ3 overexpressed cancer cells was further incorporated to the surface of the NPs. The delivery system based on PEGylated CPE is easy to fabricate, which integrates the merits of targeted cancer cell image, chemotherapeutic drug delivery, and photodynamic therapy, making it promising for cancer treatment.
机译:已经开发了基于聚(乙二醇)(PEG)接枝共轭聚电解质(CPE)的药物递送系统,以用作光敏剂和化学疗法相结合的聚合物光敏剂和药物载体。两亲刷状共聚物可以在水性介质中自组装成胶束纳米颗粒(NPs),其中疏水共轭聚电解质主链为核心,亲水PEG为壳。 NP的平均直径约为100 nm,最大吸收和发射最大分别在502和598 nm,使其适合生物成像应用。此外,CPE本身可以用作光敏剂,这不仅使NPs成为药物的载体,而且使NPs成为光动力疗法的光敏单元,从而导致癌症的化学和光动力疗法的常规组合。联合疗法对U87-MG细胞的最大半数抑制浓度(IC_(50))值为12.7μgmL〜(-1),远低于单纯光动力疗法的最大抑制浓度(IC_(50))(25.5μgmL〜(- 1))或化疗(132.8μgmL〜(-1))。为了提高系统的肿瘤特异性,将环状精氨酸-甘氨酸-天冬氨酸(cRGD)三肽作为整联蛋白α_vβ3过表达的癌细胞的受体进一步掺入NP的表面。基于PEG化CPE的递送系统易于制造,它融合了靶向癌细胞图像,化学治疗性药物递送和光动力疗法的优点,使其有望用于癌症治疗。

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