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首页> 外文期刊>Journal of the Serbian Chemical Society >Preparation and in vitro drug delivery response of doxorubicin loaded PAA coated magnetite nanoparticles
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Preparation and in vitro drug delivery response of doxorubicin loaded PAA coated magnetite nanoparticles

机译:阿霉素负载PAA包覆磁铁矿纳米颗粒的制备及体外释药反应

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In this study, spherical superparamagnetic iron oxide nanoparticles (SPION) with mean diameter of 6 nm were prepared by means of a reduction-precipitation method. The surface of SPION were coated with poly(acrylic acid) 5000 (PAA-5000) and followed by loading of anticancer drug doxorubicin. Drug loading efficiency was (14.64 ± 0.29). In vitro drug release studies were done for 8 h at two different pH (4.2 and 7.4) and drug release rates at pH 4.2 (100% DOX released in 2 h) was much faster than that at pH 7.4 (~78% DOX released in 8 h). These results indicate that these DOX-carrier nanoparticles have a high drug loading capacity and favorable release property for magnetic drug targeting. Kinetic drug release followed Korsmeyer-Peppas model at pH 4.2 while at pH 7.4 zero order model was best fitted, and drug release mechanism followed super case II transport in acidic and basic medium. The samples were characterized by XRD, SEM, TEM, FTIR, and UV-Vis.
机译:在这项研究中,通过还原沉淀法制备了平均直径为6 nm的球形超顺磁性氧化铁纳米粒子(SPION)。在SPION的表面涂上聚丙烯酸5000(PAA-5000),然后加载抗癌药阿霉素。载药效率为(14.64±0.29)。在两个不同的pH值(4.2和7.4)下进行了8小时的体外药物释放研究,在pH 4.2(2小时内释放100%DOX)下的药物释放速率比在pH 7.4(约78%DOX释放)下的药物释放速率快得多。 8小时)。这些结果表明,这些DOX载体纳米颗粒具有高的药物负载能力和对于磁性药物靶向的有利的释放性质。在pH值为4.2时,动力学药物的释放遵循Korsmeyer-Peppas模型,而在pH值为7.4时,最佳拟合为零阶模型,药物释放的机理与超级案例II在酸性和碱性介质中的运输有关。通过XRD,SEM,TEM,FTIR和UV-Vis对样品进行表征。

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