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Simultaneous electrochemical detection of multiple antibiotic residues in milk based on aptamers and quantum dots

机译:基于适体和量子点的电化学同时检测牛奶中多种抗生素残留

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摘要

A sensitive simultaneous detection of streptomycin (STR), chloramphenicol (CHL) and tetracycline (TET) residues was achieved based on aptamers and quantum dot (QD) tags. Three complementary DNA1 sequences (cDNA1s) were first designed, which are not only complementary to corresponding aptamer DNAs (Ap-DNAs) specific for STR, CHL and TET, but also complementary to part of capture DNAs (Cap-DNAs) and part of complementary DNA2s (cDNA2s), respectively. cDNA1s initially hybridize with corresponding Ap-DNAs to form duplex DNAs. However, when the target antibiotics are present, STR, CHL and TET can bind with their Ap-DNAs specifically with higher affinity, which leads to the release of cDNA1s. Then the liberated cDNA1s hybridize with corresponding Cap-DNAs which are immobilized on the surface of a gold electrode by self-assembly. After that, the prepared PbS, CdS and ZnS QDs-tagged cDNA2s further hybridize with the other ends of corresponding cDNA1s on the electrode surface. The captured QDs yield distinct electrochemical signals after acid dissolution, which reflect the type and concentration of target antibiotics. Due to the inherent amplification feature of QD tags, the low detection limits for STR, CHL and TET reached 10 nM, 5 nM and 20 nM, respectively. In addition, the established assay was applied in the detection of STR, CHL and TET residues in milk samples and showed similar response ranges.
机译:基于适体和量子点(QD)标签,可以灵敏地同时检测链霉素(STR),氯霉素(CHL)和四环素(TET)残基。首先设计了三个互补的DNA1序列(cDNA1s),它们不仅与STR,CHL和TET特异的相应适体DNA(Ap-DNA)互补,而且与捕获DNA(Cap-DNA)的一部分和互补的一部分互补DNA2s(cDNA2s)。 cDNA1s最初与相应的Ap-DNA杂交形成双链DNA。但是,当存在目标抗生素时,STR,CHL和TET可以与它们的Ap-DNA特异性结合,并具有更高的亲和力,从而导致cDNA1s的释放。然后,释放的cDNA1s与相应的Cap-DNA杂交,后者通过自组装固定在金电极的表面上。之后,制备的PbS,CdS和ZnS QDs标签的cDNA2s进一步与电极表面上相应cDNA1s的另一端杂交。酸溶解后,捕获的QD产生独特的电化学信号,反映了目标抗生素的类型和浓度。由于QD标签固有的扩增功能,STR,CHL和TET的低检测限分别达到10 nM,5 nM和20 nM。此外,已建立的检测方法用于牛奶样品中STR,CHL和TET残留的检测,并显示出相似的响应范围。

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