适体
电化学发光
检出限
纳米复合材料
电极
卡那霉素
二茂铁
材料科学
化学
组合化学
猝灭(荧光)
纳米技术
荧光
电化学
色谱法
分子生物学
生物化学
量子力学
生物
基因
物理
物理化学
作者
Xing-Pei Liu,Jin-long Cheng,Chang‐Jie Mao,Mingzai Wu,Jingshuai Chen,Bao Kang Jin
标识
DOI:10.1016/j.microc.2021.106928
摘要
In this paper, carboxylated C3N4 (g-C3N4-COOH) was prepared by a new method, and then combined with ZnSe quantum dots (QDs) through amide reaction to form g-C3N4-COOH/ZnSe nanocomposite and used for detecting kanamycin. The prepared g-C3N4-COOH/ZnSe nanocomposite was used as the subatrate of aptasensor. Then, the g-C3N4-COOH/ZnSe nanocomposite-modified electrode was incubated with aptamer DNA (NH2-DNA), after cholamine blocked the unbond sites of the electrode surface, the ferrocene-labled quenching probe (Fc-DNA) as electrochemiluminescence (ECL) signal quencher was incubated on the electrode surface through base complementation with aptamer DNA. In the absence of kanamycin, the ECL signal was quenched effectively by Fc-DNA. On the contrary, kanamycin was specifically bond with aptamer DNA, and Fc-DNA was detached from the aptasensor electrode surface because of the deformation of aptamer DNA, generating an effectively enhanced ECL signal. The aptasensor exhibited a wide detection range for detecting kanamycin (1.0 nM − 100 μM) with a low limit of detection (0.7982 nM). The prepared aptasensor displayed a stable and selective detection for kanamycin, and also provided a promising strategy for a variety of other protein target.
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