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具有优越过氧化物酶样活性的 CoSe 空心微球用于超灵敏比色生物传感。

CoSe hollow microspheres with superior oxidase-like activity for ultrasensitive colorimetric biosensing.

机构信息

College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

出版信息

Talanta. 2020 Aug 15;216:121009. doi: 10.1016/j.talanta.2020.121009. Epub 2020 Apr 10.

Abstract

As one of the transition metal dichalcogenide, CoSe has received much attention because of its superior physicochemical properties. In this work, a self-templated approach was proposed for constructing CoSe hollow microspheres by utilizing ZIF-67 hollow sphere as a template. In the followed selenylation process, selenium vapor reacts with cobalt ion in ZIF-67 to form CoSe microspheres. The obtained CoSe microspheres retain the cavity of the ZIF-67 and massive uniformly dispersed CoSe nanoparticles are embedded throughout carbon walls. The hollow interior and porous structure of CoSe microspheres provide an enhanced surface-volume ratio and short charge/mass transfer distance. The CoSe microspheres show a typical oxidase-like property able to promote 3,3',5,5'-tetramethylbenzidine (TMB) oxidation by dissolved oxygen to produce an intensive color reaction. Reactive oxygen species trials demonstrate that ·OH, O and O radicals coexist in the TMB-CoSe system. Based on its inhibitive role, a rapid and ultrasensitive determination of glutathione was reached, showing four orders of magnitude linear range from 0.005 to 10 μM and a limit of detection of 4.62 nM (S/N = 3). The assay has been successfully used to glutathione determination in practical samples.

摘要

作为过渡金属二硫属化物之一,CoSe 因其优异的物理化学性质而受到广泛关注。在这项工作中,我们提出了一种自模板法,通过利用 ZIF-67 空心球作为模板来构建 CoSe 空心微球。在随后的硒化过程中,硒蒸气与 ZIF-67 中的钴离子反应,形成 CoSe 微球。所得到的 CoSe 微球保留了 ZIF-67 的空腔,并且大量均匀分散的 CoSe 纳米颗粒嵌入到碳壁中。CoSe 微球的空心内部和多孔结构提供了增强的表面积-体积比和短的电荷/质量转移距离。CoSe 微球表现出典型的氧化酶样性质,能够促进溶解氧氧化 3,3',5,5'-四甲基联苯胺(TMB),产生强烈的颜色反应。活性氧物种试验表明,在 TMB-CoSe 体系中存在·OH、O 和 O自由基。基于其抑制作用,实现了对谷胱甘肽的快速和超灵敏测定,其线性范围从 0.005 到 10 μM,检测限为 4.62 nM(S/N = 3)。该测定法已成功用于实际样品中谷胱甘肽的测定。

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