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Characterization and application of quantum dot nanocrystal-monoclonal antibody conjugates for the determination of sulfamethazine in milk by fluoroimmunoassay

机译:量子点纳米晶体-单克隆抗体偶联物的表征及荧光免疫法测定牛奶中的磺胺二甲嘧啶

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Quantum dot (Qdot) nanocrystals have been increasingly used as fluorescence labels in fluoroimmunoassays recently because of their excellent optical characteristics. In this paper, a new monoclonal antibody (MAb) against sulfamethazine (SMZ) was successfully produced and linked to Qdot nanocrystals by covalent coupling. The Qdot-MAb conjugates were characterized by SDS-PAGE and high-performance capillary electrophoresis (HPCE). An enzyme-linked immunosorbent assay (ELISA) method was utilized to evaluate the antigen-antibody binding affinity and then a novel direct competitive fluorescence-linked immunosorbent assay (cFLISA) for the detection of SMZ in milk by using Qdots as fluorescent labels was evaluated. The results showed that the 50% inhibition values (IC50) of the cFLISA were 4.3 ng/mL in milk and 5.2 ng/mL in PBS, and the limits of detection (LODs) were 0.6 ng/mL in milk and 0.4 ng/mL in PBS, respectively. The recoveries of SMZ from spiked milk samples at levels of 10-100 ng/mL ranged from 94 to 106%, with coefficients of variation (CVs) of 2.1-9.2%.
机译:量子点(Qdot)纳米晶体由于其出色的光学特性,最近已越来越多地用作荧光免疫测定中的荧光标记。在本文中,成功生产了一种新的抗磺胺二甲嘧啶(SMZ)的单克隆抗体(MAb),并通过共价偶联与Qdot纳米晶体连接。 Qdot-MAb共轭物通过SDS-PAGE和高效毛细管电泳(HPCE)进行表征。利用酶联免疫吸附法(ELISA)评估抗原-抗体的结合亲和力,然后评估一种新的直接竞争荧光链接免疫吸附法(cFLISA),以Qdots作为荧光标记物检测牛奶中的SMZ。结果表明,牛奶中cFLISA的50%抑制值(IC50)为4.3 ng / mL,PBS中为5.2 ng / mL,检测限(LODs)分别为0.6 ng / mL和0.4 ng / mL分别在PBS中。从加标牛奶样品中10-100 ng / mL的SMZ的回收率在94%至106%之间,变异系数(CV)为2.1-9.2%。

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