Novel inner filter effect-based fluorescence immunoassay with gold nanoclusters for bromadiolone detection in human serum

被引:19
|
作者
Li, Hongfang [1 ]
Wen, Kai [1 ]
Dong, Baolei [1 ]
Zhang, Jing [2 ]
Bai, Yuchen [1 ]
Liu, Minggang [1 ]
Li, Peipei [1 ]
Mujtaba, Mari Ghulam [1 ]
Yu, Xuezhi [1 ]
Yu, Wenbo [1 ]
Ke, Yuebin [3 ]
Shen, Jianzhong [1 ]
Wang, Zhanhui [1 ]
机构
[1] China Agr Univ, Beijing Key Lab Detect Technol Anim Derived Food, Beijing Lab Food Qual & Safety, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Beijing 100193, Peoples R China
[2] Beijing Res Ctr Prevent Med, Beijing Key Lab Diagnost & Traceabil Food Poisoni, Beijing 100013, Peoples R China
[3] Shenzhen Ctr Dis Control & Prevent, Key Lab Mol Epidemiol Shenzhen, Shenzhen 518020, Peoples R China
基金
国家重点研发计划;
关键词
Bromadiolone; Poisoning diagnosis; Fluorescence immunoassay; Monoclonal antibody; LINKED-IMMUNOSORBENT-ASSAY; TANDEM MASS-SPECTROMETRY; ANTICOAGULANT RODENTICIDES; SENSITIVE DETECTION; LUMINESCENT; BRODIFACOUM; ANIMALS; ACID;
D O I
10.1016/j.snb.2019.126787
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Bromadiolone (BRD) is a widely used second-generation rodenticide and BRD poisoning in humans is relatively common. However, few rapid diagnostic methods for BRD poisoning are currently available. In this study, a highly sensitive and specific fluorescence immunoassay was developed for the rapid detection of BRD in human serum. Briefly, two novel BRD haptens were synthesized, a sensitive and specific mAb for BRD (15C1) was produced. We then incorporated mAb 15C1 as a detection reagent, and gold nanoclusters (AuNCs) as a fluorescent probe into an alkaline phosphatase-based competitive fluorescence immunoassay. The sensitivity of the immunoassay was significantly improved by introducing the fluorescence signal of the AuNCs through the facile inner-filter effect strategy. Our fluorescence immunoassay exhibited high specificity and achieved a limit of detection of 0.047 ng/mL for BRD, which was > 10 times better than the corresponding standard enzyme-linked immunosorbent assay using the same immune reagents. The recoveries in spiked human serum were 77.9%-85.6% with coefficients of variation (CVs) of 3.6%-9.8%. There was a good correlation (R-2 = 0.987) between the fluorescence immunoassay and ultra-performance liquid chromatography-tandem mass spectrometry. The fluorescence immunoassay could provide a valuable clinical tool for the rapid diagnosis of BRD poisoning.
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页数:9
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