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Synthesis and characterization of Polylactide/ Doxorubicin/Magnetic nanoparticles composites for drug delivery

机译:聚乳糖/多柔比蛋白/磁性纳米粒子复合材料的合成与表征用于药物递送

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Magnetic iron oxide nanoparticles have potential to transform conventional therapeutics, through targeted delivery by external magnetic field modulation. Conventional drug delivery lacks specificity; both normal and infected cells are exposed to toxic drugs. Consequently, the toxicity towards healthy cells leads to detrimental side effects which are formidable. However, iron oxide research in biomedicine has been hindered by their lack of stability. This study reports on the stabilization of iron oxide by polylactide (PLA). Besides affording stable iron oxide, PLA is also good for sustained delivery of the drug. PLA/doxorubicin/magnetic nanoparticles (PLA/DOX/MNPs) spheres were synthesized by solvent evaporation method and DOX anticancer drug was encapsulated. The spheres were characterized using scanning electron microscope, Fourier transform infrared microscope, thermogravimetric analyzer and UV-visible spectroscopy, which ascertained formation of the anticipated spheres and incorporation of DOX. In vitro drug release studies were carried out in both phosphate buffer (pH 7.4) and acetate buffer (pH 4.6) and they showed the same trend in both mediums. Drug release kinetics followed Higuchi model, which proved drug release by diffusion via a diffusion gradient.
机译:磁性氧化铁纳米粒子具有通过外部磁场调制的靶向递送来改变常规治疗的潜力。常规药物递送缺乏特异性;正常和受感染的细胞都暴露于有毒药物。因此,对健康细胞的毒性导致可生活的副作用。然而,生物医学的氧化铁研究已经受到缺乏稳定性的阻碍。该研究报告了聚丙烯酯(PLA)稳定氧化铁。除了提供稳定的氧化铁之外,PLA还适合持续递送药物。通过溶剂蒸发方法合成PLA / Doxorubicin /磁性纳米粒子(PLA / DOX / MNP)球体,并将DOX抗癌药物包封。使用扫描电子显微镜,傅里叶变换红外显微镜,热重分析仪和UV可见光光谱来表征球体,其确定了预期球体的形成和DOX的掺入。体外药物释放研究在磷酸盐缓冲液(pH7.4)和乙酸盐缓冲液(pH4.6)中进行,它们在两个介质中显示出相同的趋势。药物释放动力学遵循HIGUCHI模型,通过扩散梯度扩散证明了药物释放。

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