Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
7232880 | Biosensors and Bioelectronics | 2015 | 6 Pages |
Abstract
In this work, a double-probe based immunoassay was developed for rapid and sensitive determination of β-casein in bovine milk samples. In the method, magnetic beads (MBs), employed as supports for the immobilization of anti-β-casein polyclonal antibody (PAb), were used as the capture probe. Colloidal gold nanoparticles (AuNPs), employed as a bridge for loading anti-β-casein monoclonal antibody (McAb) and horseradish peroxidase (HRP), were used as the amplification probe. The presence of β-casein causes the sandwich structures of MBs-PAb-β-casein-McAb-AuNPs through the interaction between β-casein and the anti-β-casein antibodies. The HRP, used as an enzymatic-amplified tracer, can catalytically oxidize the substrate 3,3â²,5,5â²-tetramethylbenzidine (TMB), generating optical signals that are proportional to the quantity of β-casein. The linear range of the immunoassay was from 6.5 to 1520 ng mLâ1. The limit of detection (LOD) was 4.8 ng mLâ1 which was 700 times lower than that of MBs-antibody-HRP based immunoassay and 6-7 times lower than that from the microplate-antibody-HRP based assay. The recoveries of β-casein from bovine milk samples were from 95.0% to 104.3% that had a good correlation coefficient (R2=0.9956) with those obtained by an official standard Kjeldahl method. For higher sensitivity, simple sample pretreatment and shorter time requirement of the antigen-antibody reaction, the developed immunoassay demonstrated the viability for detection of β-casein in bovine milk samples.
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Physical Sciences and Engineering
Chemistry
Analytical Chemistry
Authors
Y.S. Li, X.Y. Meng, Y. Zhou, Y.Y. Zhang, X.M. Meng, L. Yang, P. Hu, S.Y. Lu, H.L. Ren, Z.S. Liu, X.R. Wang,