脱氧核酶
生物传感器
化学
法拉第电流
检出限
电极
基质(水族馆)
电化学
二茂铁
硫醇
镁
二价
无机化学
分析化学(期刊)
参比电极
色谱法
生物化学
物理化学
有机化学
海洋学
地质学
作者
Xiaoyao Gao,Huiming Huang,Shuiying Niu,Huazhen Ye,Zhenyu Lin,Bin Qiu,Guonan Chen
出处
期刊:Analytical Methods
[The Royal Society of Chemistry]
日期:2012-01-01
卷期号:4 (4): 947-947
被引量:16
摘要
A DNAzyme-based electrochemical biosensor for magnesium ion (Mg2+) has been developed. Firstly, the Mg2+-dependent DNAzyme with thiol at the 5′-terminus is immobilized on a gold electrode through thiol–Au interaction. Then the substrate strand with ferrocene (Fc) at the 5′-terminus is attached to the gold electrode via hybridization with DNAzyme. In the absence of Mg2+, this sensor shows an obvious faradaic current from Fc. In the presence of Mg2+, the Fc-labeled substrate strand is cleaved into two pieces by catalytic action of DNAzyme and moves away from the electrode surface, which reduces the faradaic current. The current change provides quantitative measurement of Mg2+. The linear response range for the proposed biosensor is 0.2–5.0 mmol L−1, and the detection limit is 0.05 mmol L−1. Other divalent metals present do not interfere with Mg2+ detection. The sensor was applied to detect Mg2+ in serum with satisfactory results.
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