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利用 DNA zyme 和单壁碳纳米管检测水中的 Pb(II)。

Combing DNAzyme with single-walled carbon nanotubes for detection of Pb(II) in water.

机构信息

Department of Chemistry, University of California, Riverside, 92507, USA.

出版信息

Analyst. 2011 Feb 21;136(4):764-8. doi: 10.1039/c0an00709a. Epub 2010 Dec 13.

Abstract

A sensitive and simple assay for the detection of Pb(2+) in aqueous solutions is reported. It takes advantage of the high affinity between single-stranded DNA (ssDNA) and single-walled carbon nanotubes (SWCNT) as well as the capability of SWCNT in fluorescence quenching. Lead(II) catalyzes the cleavage of a fluorescently labeled DNA substrate by a DNAzyme, which releases the single-stranded product to be adsorbed onto a SWCNT. The decrease in fluorescence is proportional to the Pb(2+) concentration. Concentrations as low as 1 nM Pb(2+) in water could be detected and the detection range spans over 5 orders of magnitude. The unique combination of Pb-specific DNAzyme with SWCNT produces a universal, facile and cost-effective sensing platform for lead ions. The concept can be applied to the design of detection assays for other metal ions or small molecules.

摘要

报道了一种用于检测水溶液中 Pb(2+)的灵敏而简单的分析方法。它利用了单链 DNA(ssDNA)与单壁碳纳米管(SWCNT)之间的高亲和力以及 SWCNT 荧光猝灭的能力。Pb(II) 可以催化 DNA 酶切割荧光标记的 DNA 底物,从而释放出单链产物并被吸附到 SWCNT 上。荧光强度的降低与 Pb(2+)浓度成正比。在水中,低至 1 nM 的 Pb(2+)浓度都可以被检测到,检测范围跨越了 5 个数量级。这种 Pb 特异性 DNA 酶与 SWCNT 的独特组合为铅离子提供了一种通用、简便且经济高效的传感平台。该概念可应用于其他金属离子或小分子的检测分析方法的设计。

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