Subbiah Kalaignana Selvi, Beedu Sashidhar Rao
Department of Biochemistry, University College of Science, Osmania University, Hyderabad 500 007, Telangana, India.
IET Nanobiotechnol. 2018 Dec;12(8):1047-1055. doi: 10.1049/iet-nbt.2018.5135.
This study reports an eco-friendly-based method for the preparation of biopolymer Ag-Au nanoparticles (NPs) by using gum kondagogu (GK; ), as both reducing and protecting agent. The formation of GK-(Ag-Au) NPs was confirmed by UV-absorption, fourier transformed infrared (FTIR), atomic force microscopy (AFM), scanning electron microscope (SEM) and transmission electron microscope (TEM). The GK-(Ag-Au) NPs were of 1-12 nm in size. The anti-proliferative activity of nanoparticle constructs was assessed by MTT assay, confocal microscopy, flow cytometry and quantitative real-time polymerase chain reaction (PCR) techniques. Expression studies revealed up-regulation of p53, caspase-3, caspase-9, peroxisome proliferator-activated receptors (PPAR) PPARa and PPARb, genes and down-regulation of Bcl-2 and Bcl-x(K) genes, in B16F10 cells treated with GK-(Ag-Au) NPs confirming the anti-proliferative properties of the nanoparticles.
本研究报道了一种基于环保理念的方法,通过使用贡达古胶(GK)作为还原剂和保护剂来制备生物聚合物银金纳米颗粒(NPs)。通过紫外吸收、傅里叶变换红外光谱(FTIR)、原子力显微镜(AFM)、扫描电子显微镜(SEM)和透射电子显微镜(TEM)确认了GK-(Ag-Au) NPs的形成。GK-(Ag-Au) NPs的尺寸为1-12纳米。通过MTT法、共聚焦显微镜、流式细胞术和定量实时聚合酶链反应(PCR)技术评估了纳米颗粒构建体的抗增殖活性。表达研究显示,在用GK-(Ag-Au) NPs处理的B16F10细胞中,p53、半胱天冬酶-3、半胱天冬酶-9、过氧化物酶体增殖物激活受体(PPAR)PPARα和PPARβ基因上调,而Bcl-2和Bcl-x(K)基因下调,这证实了纳米颗粒的抗增殖特性。