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A novel aptamer-quantum dot fluorescence probe for specific detection of antibiotic residues in milk

机译:一种新型适体-量子点荧光探针,可特异性检测牛奶中的抗生素残留

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Herein, a facile, signal-on and homogenous fluorescence assay using novel aptamer-dsDNA antibody-quantum dot probes was designed for detecting antibiotic residues. In this assay, the fluorescent probes were fabricated by using a double-stranded DNA antibody (dsDNA Ab) covalently bonded on the surface of CdSe quantum dots. The antibody can bind double-stranded DNA (dsDNA) specifically. When dsDNA was added, the fluorescence could be efficiently quenched because the probes came into contact with each other with dsDNA as the bridge. The dsDNA was formed between an aptamer towards chloromycetin (CAP) and its complementary strand DNA (cDNA). When CAP was added into the reaction system, the aptamer reacted with CAP preferentially and the dsDNA was unwinded to single strand DNA (ssDNA) which cannot be recognized by the dsDNA antibody. Thus the probes were separated and fluorescence was recovered. Based on the scheme, a signal-on fluorescence assay for detecting antibiotics in a homogenous aqueous phase was developed. Under the optimized conditions, the assay shows a good liner range from 0.05 ng mL(-1) to 100 ng mL(-1) and the limit of detection (LOD) is 0.002 ng mL(-1). If the analyte is changed, the assay can also be employed only by changing the corresponding aptamer and its cDNA. What's more, the probes can be reused at least 10 times with the recovery above 90%. The fluorescence assay is facile and has promising application for detecting antibiotic contaminants in biological and environmental samples.
机译:本文中,设计了一种使用新型适体-dsDNA抗体-量子点探针的简便,信号开启且均质的荧光检测试剂,用于检测抗生素残留。在该测定中,通过使用共价结合在CdSe量子点表面上的双链DNA抗体(dsDNA Ab)来制备荧光探针。该抗体可以特异性结合双链DNA(dsDNA)。当添加dsDNA时,由于探针以dsDNA为桥梁相互接触,因此可以有效地猝灭荧光。在针对氯霉素的适体(CAP)与其互补链DNA(cDNA)之间形成了dsDNA。当将CAP添加到反应系统中时,适体与CAP优先反应,并且dsDNA解链为dsDNA抗体不能识别的单链DNA(ssDNA)。因此分离探针并回收荧光。基于该方案,开发了一种信号荧光检测法,用于检测均质水相中的抗生素。在优化的条件下,该测定显示了良好的线性范围,从0.05 ng mL(-1)到100 ng mL(-1),检出限(LOD)为0.002 ng mL(-1)。如果改变了分析物,则也只能通过改变相应的适体及其cDNA来使用该测定法。此外,探针可以重复使用至少10次,回收率达到90%以上。荧光测定法简便易行,在检测生物和环境样品中的抗生素污染物方面具有广阔的应用前景。

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