首页> 外文期刊>Materials science & engineering >Development of biodegradable PLGA nanoparticles surface engineered with hyaluronic acid for targeted delivery of paclitaxel to triple negative breast cancer cells
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Development of biodegradable PLGA nanoparticles surface engineered with hyaluronic acid for targeted delivery of paclitaxel to triple negative breast cancer cells

机译:透明质酸表面修饰的可生物降解PLGA纳米颗粒的开发,可将紫杉醇靶向递送至三阴性乳腺癌细胞

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摘要

This study aimed at development of poly (lactic-co-glycolic acid) (PLGA) nanoparticles embedded with paclitaxel and coated with hyaluronic acid (HA-PTX-PLGA) to actively target the drug to a triple negative breast cancer cells. Nanoparticles were successfully fabricated using a modified oil-in-water emulsion method. The effect of various formulations parameters on the physicochemical properties of the nanoparticles was investigated. SEM imaging confirmed the spherical shape and nano-scale size of the nanoparticles. A sustained drug release profile was obtained and enhanced PTX cytotoxicity was observed when MDA-MB-231 cells were incubated with the HA-PTX-PLGA formulation compared to cells incubated with the non-HA coated nanoparticles. Moreover, HA-PLGA nanoparticles exhibited improved cellular uptake, based on a possible receptor mediated endocytosis due to interaction of HA with CD44 receptors when compared to non-coated PLGA nanoparticles. The non-haemolytic potential of the nanoparticles indicated the suitability of the developed formulation for intravenous administration.
机译:这项研究旨在开发嵌入紫杉醇并涂有透明质酸(HA-PTX-PLGA)的聚(乳酸-乙醇酸)(PLGA)纳米颗粒,以将药物积极靶向三阴性乳腺癌细胞。使用改进的水包油乳液方法成功地制备了纳米颗粒。研究了各种配方参数对纳米颗粒理化性质的影响。 SEM成像证实了纳米颗粒的球形和纳米级尺寸。当将MDA-MB-231细胞与HA-PTX-PLGA制剂温育时,与未与HA包被的纳米颗粒温育的细胞相比,获得了持续的药物释放曲线,并观察到增强的PTX细胞毒性。此外,基于HA-与未包被的PLGA纳米颗粒相比,由于HA与CD44受体的相互作用,基于可能的受体介导的内吞作用,HA-PLGA纳米颗粒表现出改善的细胞摄取。纳米颗粒的非溶血潜力表明了所开发的制剂适合静脉内给药。

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