首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >A carbon dot and gold nanoparticle-based fluorometric immunoassay for 8-hydroxy-2-deoxyguanosine in oxidatively damaged DNA
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A carbon dot and gold nanoparticle-based fluorometric immunoassay for 8-hydroxy-2-deoxyguanosine in oxidatively damaged DNA

机译:基于碳点和金纳米粒子的含8-羟基-2-脱氧核苷酸的碳点和金纳米粒子荧光测定免疫测定液中的氧化损伤DNA

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摘要

A method is described for the fluorometric determination of DNA containing oxidatively damaged product 8-hydroxy-2-deoxyguanosine (DNA-8-OHdG). Carbon dots (CDs) were modified with glutaraldehyde for DNA conjugation, and antibody against 8-OHdG was immobilized on gold nanoparticles (AuNPs). The presence of DNA-8-OHdG can be linked to CDs by reaction of amino groups on DNA with glutaraldehyde. AuNPs were brought closely to CDs by specific immune reaction between 8-OHdG and antibody on AuNPs. Under 350nm photoexcitation, the emission of CDs with a peak at 440nm is quenched by the AuNPs and not restored. In the presence of DNA-8-OHdG, the measured fluorescence intensity decreases and quenching efficiency increases. The limit of detection is 700 pM, and the assay works in the 0.01nM to 25M DNA-8-OHdG concentration range. The method is perceived to possess a good potential as a tool for detecting biomarkers for DNA damage due to oxidative stress.
机译:描述了含有氧化损坏产物8-羟基-2-脱氧核苷酸(DNA-8-OHDG)的DNA的荧光测定方法。 用戊二醛(CD)用戊二醛进行DNA缀合的碳点(CD),并固定8-OHDG的抗体在金纳米粒子(AUNP)上固定。 DNA-8-OHDG的存在可以通过氨基与戊二醛的DNA反应与CDS连接。 通过在8-OHDG和AUNPS上的抗体之间的特异性免疫反应密切地与CDS紧密地带来。 在350nm的光透明度下,耳孔淬灭440nm峰值的CD的发射是抗损伤的。 在DNA-8-OHDG的存在下,测量的荧光强度降低,淬火效率增加。 检测限为700 pm,测定在0.01nm至25m的DNA-8-OHDG浓度范围内。 该方法被认为具有作为检测由于氧化应激引起的DNA损伤的生物标志物的工具的良好潜力。

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