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One pot synthesis of doxorubicin loaded gold nanoparticles for sustained drug release

机译:一锅合成阿霉素负载的金纳米颗粒以持续释放药物

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摘要

Here, we report a facile, versatile and simple one-pot synthesis of doxorubicin (Dox) loaded gold nanoparticles (Dox-GNP conjugate), where Dox can act both as a reducing as well as a capping agent. Interestingly, when the conjugate was placed into the transporter protein environment, it avoided the undesirable multilayer protein corona formation, which is very common for nanomaterials. The in vitro drug release kinetic studies and the cytotoxicity assay and cellular update efficiency advocates that the system is capable of sustained release of the drug even in the presence of a complex biological environment.
机译:在这里,我们报告了阿霉素(Dox)负载的金纳米颗粒(Dox-GNP共轭物)的简便,通用和简单的一锅合成方法,其中Dox既可以充当还原剂,也可以充当封端剂。有趣的是,当将缀合物放置在转运蛋白环境中时,它避免了不希望的多层蛋白电晕的形成,这对纳米材料来说是很常见的。体外药物释放动力学研究以及细胞毒性测定和细胞更新效率提倡该系统即使在复杂的生物环境中也能够持续释放药物。

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