4.8 Article

Tailoring the Photoelectrochemical Activity of Hexametaphosphate-Capped CdS Quantum Dots by Ca2+-Triggered Surface Charge Regulation: A New Signaling Strategy for Sensitive Immunoassay

期刊

ANALYTICAL CHEMISTRY
卷 93, 期 41, 页码 13783-13790

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c02284

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资金

  1. NSFC [22074039, 21305041, 21705045]
  2. Training Program for Huxiang Youth Science and Technology Innovation Talents [2018RS3062]
  3. Hunan Provincial Natural Science Foundation [2019JJ50385]
  4. Hunan Provincial Education Department Project [19C1153]
  5. Training Program for Excellent Young Innovators of Changsha [KQ2009043]

向作者/读者索取更多资源

This study presents a new strategy for sensitive PEC immunoassay by modifying the surface charge of photoactive materials. By utilizing CaCO3 nanoparticles as labels to regulate the surface charge of CdS@HMP QDs, sensitive detection of CEA is achieved with a linear detection range of 0.005-50 ng mL(-1) and a detection limit of 1 pg mL(-1).
The development of efficient signaling strategies is highly important for photoelectrochemical (PEC) immunoassay. We report here a new and efficient strategy for sensitive PEC immunoassay by tailoring the electrostatic interaction between the photoactive material and the electron donor. The photoelectric conversion of hexametaphosphate (HMP)-capped CdS quantum dots (QDs) in Na2SO3 solution is significantly boosted after Ca2+ incubation. The negative surface charges on CdS@HMP QDs decrease because of the complexation reaction between HMP and Ca2+, and the electrostatic repulsion between CdS@HMP QDs and electron donor (SO32-) becomes weak accordingly, leading to an improved electron-hole separation efficiency. Inspired by the PEC response of CdS@HMP QDs to Ca2+, a novel signal-on PEC immunoassay platform is established by employing CaCO3 nanoparticles as labels. By regulating the surface charge of CdS@HMP QDs with in situ-generated Ca2+ from CaCO3 labels, sensitive detection of the carcinoembryonic antigen (CEA) is achieved. The linear detection range is 0.005-50 ng mL(-1) and the detection limit is 1 pg mL(-1) for CEA detection. Our work not only provides a facile route to tailor the photoelectric conversion but also lays the foundation for sensitive PEC immunoassay by simply regulating the surface charge of photoactive materials.

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