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Development of a monoclonal antibody against deoxynivalenol for magnetic nanoparticle-based extraction and an enzyme-linked immunosorbent assay

Cited 18 time in Web of Science Cited 19 time in Scopus
Authors
Lee, Hyuk-Mi; Song, Sung-Ok; Cha, Sang-Ho; Wee, Sung-Bok; Bischoff, Karyn; Park, Sung-Won; Son, Seong-Wan; Kang, Hwan-Goo; Cho, Myung-Haing
Issue Date
2013-06
Citation
Journal of Veterinary Science, Vol.14 No.2, pp.143-150
Keywords
deoxynivalenol, ELISA, magnetic nanoparticles, monoclonal antibody
Abstract
Monoclonal antibody (mAb, NVRQS-DON) against deoxynivalenol (DON) was prepared. DON-Ag coated enzyme linked immunosorbent assay (ELISA) and DON-Ab coated ELISA were prepared by coating the DON-BSA and DON mAb. Quantitative DON calculation ranged from 50 to 4,000 ng/mL for DON-Ab coated ELISA and from 25 to 500 ng/mL for DON-Ag coated ELISA. 50% of inhibitory concentration values of DON, HT-2, 15-acetyl-DON, and nivalenol were 23.44, 22,545, 5,518 and 5,976 ng/mL based on the DON-Ab coated ELISA. Cross-reactivity levels of the mAb to HT-2, 15-acetyl-DON, and nivalenol were 0.1, 0.42, and 0.40 %. The intra- and interassay precision coefficient variation (CV) were both < 10 %. In the mAb-coated ELISA, mean DON recovery rates in animal feed (0 to 1,000 mu g/kg) ranged from 68.34 to 95.49% (CV; 4.10 to 13.38%). DON in a buffer solution (250, 500 and 1,000 ng/mL) was isolated using 300 mu g of NVRQS-DON and 3 mg of magnetic nanoparticles (MNPs). The mean recovery rates of DON using this mAb-MNP system were 75.2, 96.9, and 88.1% in a buffer solution spiked with DON (250, 500, and 1,000 ng/mL). Conclusively we developed competitive ELISAs for detecting DON in animal feed and created a new tool for DON extraction using mAb-coupled MNPs.
ISSN
1229-845X
URI
https://hdl.handle.net/10371/172462
DOI
https://doi.org/10.4142/jvs.2013.14.2.143
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College of Veterinary Medicine (수의과대학)Dept. of Veterinary Medicine (수의학과)Journal Papers (저널논문_수의학과)
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