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Diastase assisted green synthesis of size-controllable gold nanoparticles

机译:淀粉酶辅助绿色合成大小可控的金纳米粒子

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Diastase, a natural enzyme, was used for the one pot aqueous synthesis of gold nanoparticles (AuNPs) of tunable size. During the synthetic process, diastase acts concurrently as both a reducing and stabilizing agent, while no additional chemical reagents or surfactants are added. The formation of AuNPs was confirmed by using a UV-visible spectrophotometer, with a characteristic surface plasmon resonance (SPR) band at 530 nm. The size of the diastase-stabilized AuNPs can be easily controlled by changing the quantity of diastase. The produced AuNPs were characterized by using powder X-ray diffraction (XRD), UV-visible spectroscopy, Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). The FTIR spectrum revealed the capping of diastase on the surface of AuNPs. Furthermore, the formed gold nanoparticles are stable for more than three months. In vitro cytotoxicity studies by MTT assay on HCT116 and A549 cancer cells showed that the cytotoxicity of the assynthesized Au nanocolloids depends on their size and dose.
机译:天然酶Diastase用于一锅法合成大小可调的金纳米颗粒(AuNPs)。在合成过程中,淀粉酶同时充当还原剂和稳定剂,而没有添加其他化学试剂或表面活性剂。通过使用紫外可见分光光度计确认了AuNP的形成,该分光光度计在530 nm处具有特征性表面等离振子共振(SPR)带。稳定淀粉酶的AuNP的大小可以通过改变淀粉酶的量来容易地控制。通过使用粉末X射线衍射(XRD),紫外可见光谱,傅立叶变换红外光谱(FT-IR)和透射电子显微镜(TEM)来表征所产生的AuNP。 FTIR光谱揭示了AuNPs表面上的淀粉酶封端。此外,所形成的金纳米颗粒稳定超过三个月。通过MTT分析对HCT116和A549癌细胞进行的体外细胞毒性研究表明,合成的金纳米胶体的细胞毒性取决于其大小和剂量。

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