基于CdS/MoS2联合扩增的Pb2+超灵敏DNA酶电化学发光生物传感器

Rui Yang
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引用次数: 0

摘要

铅是对人类健康和生态环境影响最严重的重金属之一。过量的铅会导致脑发育迟缓和肝肾损伤。本文设计了一种基于CdS量子点(CdS QDs)/MoS2酶辅助多重扩增和DNA酶的电化学发光(ECL)生物传感器,实现了Pb2+的高灵敏度检测。合成了AuNPs-PDDA-MoS2配合物作为传感底物。巯基标记的T30695 DNA通过Au-S键组装在电极表面,随后DNA的氨基标记端通过酰胺键与CdS量子点连接。在Pb2+存在下,DNA序列的G碱基形成G-四聚体(G4)结构,进一步合成DNA酶。DNA酶和AuNPs-MoS2复合材料对H2O2的催化氧化导致CdS量子点的H2O2电化学发光显著降低。该传感器的检测范围为1.0×10-14 ~ 5.0×10-11mol/L (R = 0.9992),检出限为1×10-15 mol/L。该传感器可对实际水样中的Pb2+进行检测,结果令人满意。
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An DNA Enzyme Electrochemiluminescence Biosensor for Ultra-sensitive Detection of Pb2+ Based on CdS/MoS2 Joint Amplification
Lead (Pb) is one of the most serious heavy metals to human health and ecological environment. Excessive lead can lead brain retardation and liver and kidney damage. In this work, a novel electrochemiluminescence (ECL) biosensor based on CdS quantum dots (CdS QDs)/MoS2 enzyme assist multiple amplification and DNA enzyme was designed to achieve high sensitivity detection of Pb2+. AuNPs-PDDA-MoS2 complex was synthesized as sensing substrate. The thiol-labeled T30695 DNA was assembled on the surface of the electrode via Au-S bonds, following which the amino-labeled ends of the DNA were linked to the CdS QDs by the formation of amide bonds. In the presence of Pb2+, the G bases of DNA sequence formed G- tetraplex (G4) structure, DNA enzymes were then further synthesized. The catalytic oxidation of H2O2 by DNA enzyme and AuNPs-MoS2 composite resulted in a significant decrease of electrochemiluminescence of CdS QDs with H2O2. The detection range of the biosensor was 1.0×10-14 - 5.0×10-11mol/L (R = 0.9992) with a detection limit of 1×10-15 mol/L. This biosensor can detect Pb2+ in real water samples with satisfactory results.
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