适体
检出限
超分子化学
生物素化
微分脉冲伏安法
链霉亲和素
滚动圆复制
胶体金
纳米化学
生物传感器
化学
杂交探针
线性范围
电化学
电化学气体传感器
纳米技术
分析化学(期刊)
分析物
组合化学
循环伏安法
荧光
材料科学
色谱法
生物素
电极
结晶学
分子
有机化学
分子生物学
物理化学
生物
生物化学
DNA
晶体结构
DNA复制
作者
Bo Shen,Jianbo Li,Wei Cheng,Yurong Yan,Renkuan Tang,Yongguo Li,Huangxian Ju,Shijia Ding
出处
期刊:Mikrochimica Acta
[Springer Nature]
日期:2014-08-15
卷期号:182 (1-2): 361-367
被引量:42
标识
DOI:10.1007/s00604-014-1333-3
摘要
We report on a novel strategy for the electrochemical detection of cocaine. It is based on the use of a supramolecular aptamer, rolling circle amplification (RCA), and multiplex binding of a biotin-strepavidin system. The aptamer fragments were assembled to a supramolecular aptamer which, in the presence of cocaine, conjugates to streptavidin for anchoring of biotinylated circular DNA. This initiates RCA and enables sensitive electrochemical-enzymatic readout. A significant signal amplification was obtained by using streptavidin linked to alkaline phosphatase that binds to the remaining biotinylated detection probes and catalyzes the hydrolysis of the synthetic enzyme substrate α-naphthylphosphate. This dual amplification strategy tremendously increases the detection limit of the aptasensor. Under optimal conditions and using differential pulse voltammetry, cocaine can be detected in the concentration range between 2 and 500 nM with a detection limit as low as 1.3 nM (at S/N = 3). The method is specific and acceptably reproducible. It was successfully applied to the detection of cocaine in (spiked) urine samples. The data were in good agreement with those obtained by the GC-MS reference method. Cascade signal amplification strategy for cocaine electrochemical detection by supramolecular aptamer and rolling circle amplification.
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