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Hyaluronic acid co-functionalized gold nanoparticle complex for the targeted delivery of metformin in the treatment of liver cancer (HepG2 cells)

机译:透明质酸共官能化的金纳米颗粒复合物,可靶向递送二甲双胍,用于治疗肝癌(HepG2细胞)

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摘要

In this study, green synthesis of gold nanoparticles (AuNPs) was achieved using the extract of eggplant as a reducing agent. Hyaluronic acid (HA) serves as a capping and targeting agent. Metformin (MET) was successfully loaded on HA capped AuNPs (H-AuNPs) and this formulation binds easily on the surface of the liver cancer cells. The synthesized nanoparticles were characterized by UV-Vis spectrophotometer, HR-TEM, particle size analyser and zeta potential measurement. Toxicity studies of H-AuNPs in zebra fish confirmed the in vivo safety of the AuNPs. The in vitro cytotoxicity results showed that the amount of MET-H-AuNPs enough to achieve 50% inhibition (IC50) was much lower than free MET. Flow cytometry analysis showed the significant reduction in G2/M phase after treatment with MET-H-AuNPs, and molecular level apoptosis were studied using western blotting. The novelty of this study is the successful synthesis of AuNPs with a higher MET loading and this formulation exhibited better targeted delivery as well as increased regression activity than free MET in HepG2 cells. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在这项研究中,使用茄子提取物作为还原剂实现了金纳米颗粒(AuNPs)的绿色合成。透明质酸(HA)用作加帽和靶向剂。二甲双胍(MET)已成功加载到HA封端的AuNPs(H-AuNPs)上,该制剂易于结合在肝癌细胞表面。通过紫外可见分光光度计,HR-TEM,粒度分析仪和ζ电势测量对合成的纳米颗粒进行表征。 H-AuNPs在斑马鱼中的毒性研究证实了AuNPs在体内的安全性。体外细胞毒性结果表明,足以实现50%抑制(IC50)的MET-H-AuNPs量远低于游离MET。流式细胞仪分析显示,用MET-H-AuNPs处理后,G2 / M期明显减少,并使用Western印迹法研究了分子水平的细胞凋亡。这项研究的新颖之处在于成功合成了具有较高MET负载量的AuNP,并且该制剂与HepG2细胞中的游离MET相比,具有更好的靶向递送和更高的回归活性。 (C)2015 Elsevier Ltd.保留所有权利。

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