Suppr超能文献

基于 Fenton 反应的无标记比色法检测抗坏血酸:未修饰金纳米粒子探针与多种分子逻辑门。

Label-free colorimetric sensing of ascorbic acid based on Fenton reaction with unmodified gold nanoparticle probes and multiple molecular logic gates.

机构信息

Research Center for Analytical Sciences, Northeastern University, Box 332, Shenyang 110819, China.

出版信息

Anal Chim Acta. 2012 Mar 2;717:127-33. doi: 10.1016/j.aca.2011.12.037. Epub 2012 Jan 5.

Abstract

A label-free strategy based on Fenton reaction with unmodified gold nanoparticles (AuNPs) as probe is demonstrated for ascorbic acid (AA) sensing. AuNPs is stable in the presence of single stranded DNA (ssDNA) which prevents salt-induced aggregation of AuNPs in solution. The hydroxyl free radicals generated by Fenton reaction lead to ssDNA cleavage into different sequence fragments which induce aggregation of AuNPs to produce a red-to-blue color change. As an efficient biological antioxidant, AA could effectively scavenge free radicals to avoid the cleavage of ssDNA, so that it prevents color change of the AuNPs solution. Thus, the color change of AuNPs in the presence and absence of AA provides a new approach for the detection of AA. The absorbance ratio at two wavelengths, A(670)/A(520), decreases linearly with AA content within 1-15 μM, giving rise to a detection limit of 0.3 μM and a RSD of 2.8% (10 μM). The color display of AuNPs solution makes it feasible for the estimation of AA content by naked eye visualization. Moreover, based on Fenton reaction and unmodified gold nanoparticles, a multiple logic gate system includes two logic operations, i.e., INHIBIT and NOR, has been designed with small molecules (AA, l-cysteine, glutathione) as inputs and the colorimetric changes of AuNPs solution as outputs.

摘要

一种基于芬顿反应的无标记策略,使用未经修饰的金纳米粒子(AuNPs)作为探针,用于检测抗坏血酸(AA)。在单链 DNA(ssDNA)存在下,AuNPs 是稳定的,这防止了溶液中 AuNPs 因盐诱导而聚集。芬顿反应产生的羟基自由基导致 ssDNA 切割成不同的序列片段,从而诱导 AuNPs 聚集,产生红-蓝颜色变化。作为一种有效的生物抗氧化剂,AA 可以有效地清除自由基,避免 ssDNA 的断裂,从而防止 AuNPs 溶液的颜色变化。因此,AA 存在和不存在时 AuNPs 的颜色变化为 AA 的检测提供了一种新方法。在 1-15 μM 范围内,两个波长(A(670)/A(520))的吸光度比值随 AA 含量呈线性下降,检测限为 0.3 μM,相对标准偏差(RSD)为 2.8%(10 μM)。AuNPs 溶液的颜色显示使得通过肉眼可视化估计 AA 含量成为可能。此外,基于芬顿反应和未经修饰的金纳米粒子,已经设计了一个包含两个逻辑操作(INHIBIT 和 NOR)的多逻辑门系统,该系统以小分子(AA、l-半胱氨酸、谷胱甘肽)作为输入,以 AuNPs 溶液的比色变化作为输出。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验