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基于多色量子点的荧光免疫分析阵列用于同时可视化检测牛奶中的多种抗生素残留。

Multi-color quantum dot-based fluorescence immunoassay array for simultaneous visual detection of multiple antibiotic residues in milk.

机构信息

Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, People's Republic of China.

Key Laboratory of Luminescence and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, People's Republic of China.

出版信息

Biosens Bioelectron. 2015 Oct 15;72:320-5. doi: 10.1016/j.bios.2015.05.018. Epub 2015 May 7.

Abstract

Antibiotic residues, which are among the most common contaminants in animal-based food products such as milk, have become a significant public health concern. Here, we combine a multicolor quantum dot (QD)-based immunofluorescence assay and an array analysis method to achieve simultaneous, sensitive and visual detection of streptomycin (SM), tetracycline (TC), and penicillin G (PC-G) in milk. Antibodies (Abs) for SM, TC and PC-G were conjugated to QDs with different emission wavelengths (QD 520 nm, QD 565 nm and QD 610 nm) to serve as detection probes (QD-Ab). Then a direct competitive fluorescent immunoassay was performed in antigen-coated microtiter plate wells for simultaneous qualitative and quantitative detection of SM, TC, and PC-G residues, based on fluorescence of the QD-Ab probes. The linear ranges for SM, TC and PC-G were 0.01-25 ng/mL, 0.01-25 ng/mL and 0.01-10 ng/mL, respectively, with detection limit of 5 pg/mL for each of them. Based on fluorescence of the QD-Ab probes, residues of the three antibiotics were determined visually and simultaneously. Compared with a commercial enzyme-linked immunosorbent assay kit, our method could achieve simultaneous analysis of multiple target antibiotics in multiple samples in a single run (high-throughput analysis) and improved accuracy and sensitivity for analysis of residues of the three antibiotics in authentic milk samples. This new analytical tool can play an important role in ameliorating the negative impact of the residual antibiotics on human health and the ecosystem.

摘要

抗生素残留是动物源性食品(如牛奶)中最常见的污染物之一,已成为一个重大的公共卫生关注点。在这里,我们结合了基于多色量子点(QD)的免疫荧光分析和阵列分析方法,实现了牛奶中链霉素(SM)、四环素(TC)和青霉素 G(PC-G)的同时、灵敏和可视化检测。SM、TC 和 PC-G 的抗体(Abs)与具有不同发射波长的 QD(QD 520nm、QD 565nm 和 QD 610nm)偶联,用作检测探针(QD-Ab)。然后,在抗原包被的微孔板孔中进行直接竞争荧光免疫分析,基于 QD-Ab 探针的荧光,对 SM、TC 和 PC-G 残留进行定性和定量检测。SM、TC 和 PC-G 的线性范围分别为 0.01-25ng/mL、0.01-25ng/mL 和 0.01-10ng/mL,检测限均为 5pg/mL。基于 QD-Ab 探针的荧光,可直观且同时检测三种抗生素的残留。与商业酶联免疫吸附测定试剂盒相比,我们的方法可以在单次运行中(高通量分析)同时分析多个样品中的多种目标抗生素,并提高对真实牛奶样品中三种抗生素残留的分析准确性和灵敏度。这种新的分析工具可以在改善抗生素残留对人类健康和生态系统的负面影响方面发挥重要作用。

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