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无标记 DNA 酶分析法用于双扩增和一锅检测铅污染。

Label-free DNAzyme assays for dually amplified and one-pot detection of lead pollution.

机构信息

College of Biomass Science and Engineering, Healthy Food Evaluation Research Center and Key Laboratory of Food Science and Technology of Ministry of Education of Sichuan Province, Sichuan University, Chengdu 610065, China.

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Collaborative Innovation Center of Biotherapy, Chengdu, Sichuan 610041, China.

出版信息

J Hazard Mater. 2021 Mar 15;406:124790. doi: 10.1016/j.jhazmat.2020.124790. Epub 2020 Dec 7.

Abstract

Lead pollution in water and soil often transfers to food, advocating tools for on-site detection of lead pollution to ensure both environmental and food safety. We proposed a label-free, dually amplified and homogeneous DNAzyme assay for sensitive and one-pot detection of lead pollution. Instead of using chemically modified DNA substrate, a structure-response digestion process was introduced to monitor Pb presence-induced cleavage process of unlabeled substrate, further amplifying the response signals and eliminating the use of labeled DNA probes. The DNAzyme assay allowed to detect Pb as low as 0.12 nM and endued a dynamic range from 0.1 nM to 30 nM. In addition, it can specifically identify Pb among other metal ions. We demonstrated that the DNAzyme assay can precisely detect Pb in tap water, milk and fish. Thus, the DNAzyme assay is promising for on-site monitoring lead pollution risk and ensuring environmental and food safety.

摘要

水和土壤中的铅污染通常会转移到食物中,因此提倡使用现场检测铅污染的工具,以确保环境和食品安全。我们提出了一种无标记、双重放大和均相 DNA 酶分析方法,用于灵敏、一次性检测铅污染。该方法不使用化学修饰的 DNA 底物,而是引入结构-反应消化过程来监测 Pb 存在诱导的未标记底物的切割过程,从而进一步放大响应信号并消除标记 DNA 探针的使用。该 DNA 酶分析方法可以检测到低至 0.12 nM 的 Pb,并具有 0.1 nM 至 30 nM 的动态范围。此外,它可以特异性识别 Pb 与其他金属离子。我们证明了该 DNA 酶分析方法可以精确检测自来水中、牛奶中和鱼肉中的 Pb。因此,该 DNA 酶分析方法有望用于现场监测铅污染风险,确保环境和食品安全。

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