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首页> 外文期刊>Journal of Nanoparticle Research >Biodegradable thermoresponsive polymeric magnetic nanoparticles: a new drug delivery platform for doxorubicin
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Biodegradable thermoresponsive polymeric magnetic nanoparticles: a new drug delivery platform for doxorubicin

机译:可生物降解的热响应聚合物磁性纳米颗粒:阿霉素的新药物递送平台

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The use of nanoparticles as drug delivery systems for anticancer therapeutics has great potential to revolutionize the future of cancer therapy. The aim of this study is to construct a novel drug delivery platform comprising a magnetic core and biodegradable thermoresponsive shell of tri-block-copolymer. Oleic acid-coated Fe3O4 nanoparticles and hydrophilic anticancer drug “doxorubicin” are encapsulated with PEO–PLGA–PEO (polyethylene oxide–poly d, l lactide-co-glycolide–polyethylene oxide) tri-block-copolymer. Structural, magnetic, and physical properties of Fe3O4 core are determined by X-ray diffraction, vibrating sample magnetometer, and transmission electron microscopy techniques, respectively. The hydrodynamic size of composite nanoparticles is determined by dynamic light scattering and is found to be ~36.4 nm at 25 °C. The functionalization of magnetic core with various polymeric chain molecules and their weight proportions are determined by Fourier transform infrared spectroscopy and thermogravimetric analysis, respectively. Encapsulation of doxorubicin into the polymeric magnetic nanoparticles, its loading efficiency, and kinetics of drug release are investigated by UV–vis spectroscopy. The loading efficiency of drug is 89% with a rapid release for the initial 7 h followed by the sustained release over a period of 36 h. The release of drug is envisaged to occur in response to the physiological temperature by deswelling of thermoresponsive PEO–PLGA–PEO block-copolymer. This study demonstrates that temperature can be exploited successfully as an external parameter to control the release of drug.
机译:纳米粒子作为抗癌治疗药物的给药系统具有巨大的潜力,可以彻底改变癌症治疗的未来。这项研究的目的是构建一个新型的药物输送平台,该平台包括一个三嵌段共聚物的磁芯和可生物降解的热响应性外壳。油酸包覆的Fe 3 O 4 纳米颗粒和亲水性抗癌药物“阿霉素”被PEO-PLGA-PEO(聚环氧乙烷-聚d,丙交酯-co-乙交酯—聚环氧乙烷)三嵌段共聚物。 Fe 3 O 4 芯的结构,磁性和物理性质分别通过X射线衍射,振动样品磁力计和透射电子显微镜技术确定。复合纳米颗粒的流体动力学尺寸通过动态光散射确定,在25°C下约为36.4 nm。磁芯具有各种聚合物链分子的功能化及其重量比例分别通过傅立叶变换红外光谱法和热重分析法确定。通过紫外可见光谱研究了将阿霉素包封在聚合物磁性纳米粒子中,其负载效率和药物释放动力学。药物的装载效率为89%,在最初的7小时内迅速释放,然后在36小时内持续释放。通过释放热响应性PEO–PLGA–PEO嵌段共聚物,可以预期药物释放是对生理温度的响应。这项研究表明,温度可以成功地用作控制药物释放的外部参数。

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