A competitive immunoassay with a surrogate calibrator curve for aflatoxin M1 in milk

被引:42
作者
Guan, Di [1 ,2 ,3 ]
Li, Peiwu [1 ,2 ,3 ]
Cui, Yehan [4 ]
Zhang, Qi [1 ,3 ]
Zhang, Wen [1 ,2 ]
机构
[1] Chinese Acad Agr Sci, Oil Crops Res Inst, Wuhan 430062, Peoples R China
[2] Minist Agr, Key Lab Oil Crop Biol, Wuhan 430062, Peoples R China
[3] Qual Inspect & Test Ctr Oilseeds Prod MOA PRC, Wuhan 430062, Peoples R China
[4] Minist Agr, Dev Ctr Sci & Technol, Beijing 100125, Peoples R China
关键词
Aflatoxin M-1; Anti-idiotype antibody; Surrogate; Enzyme-linked immunosorbent assay; EXTRACTION; PRODUCTS; M1;
D O I
10.1016/j.aca.2011.07.011
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A green enzyme-linked immunosorbent assay (ELISA) to measure aflatoxin M-1 (AFM(1)) in milk was developed and validated with a surrogate calibrator curve. Polyclonal anti-idiotype (anti-Id) antibody, used as an AFM(1) surrogate, was generated by immunizing rabbits with F(ab')(2) fragments from the anti-AFM(1) monoclonal antibody (mAb). The rabbits exhibited high specificity to the anti-AFM(1) mAb, and no cross-reactivity to either of the other anti-aflatoxin mAbs or the isotype matched mAb was observed. After optimizing the physicochemical factors (pH and ionic strength) that influence assay performance, a quantitative conversion formula was developed between AFM(1) and the anti-Id antibody (y = 31.91x - 8.47, r = 0.9997). The assay was applied to analyze AFM(1) in spiked milk samples. The IC50 value of the surrogate calibrator curve was 2.4 mu g mL(-1), and the inter-assay and intra-assay variations were less than 10.8%; recovery ranged from 85.2 to 110.9%. A reference high-performance liquid chromatography method was used to validate the developed method, and a good correlation was obtained (y = 0.81x + 9.82, r = 0.9922). (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:64 / 69
页数:6
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