- Author:
Yong JIN
1
;
Jin Wook JANG
;
Chang Hoon HAN
;
Mun Han LEE
Author Information
- Publication Type:Research Support, Non-U.S. Gov't ; Original Article
- Keywords: competitive direct ELISA; immunochromatographic assay; kanamycin; monoclonal antibody
- MeSH: Animals; Anti-Bacterial Agents/*analysis; Antibodies, Monoclonal; Chromatography/methods/veterinary; Enzyme-Linked Immunosorbent Assay/methods/*veterinary; Kanamycin/*analysis; Mice; Milk/*chemistry; Rabbits
- From:Journal of Veterinary Science 2006;7(2):111-117
- CountryRepublic of Korea
- Language:English
- Abstract: Monoclonal antibody against kanamycin was prepared, and competitive direct ELISA and immunochromatographic assay were developed using the antibody to detect kanamycin in animal plasma and milk. The monoclonal antibody produced was identified to be IgG1, which has a kappa light chain. No cross-reactivity of the antibody was detected with other aminoglycosides, indicating that the monoclonal antibody was highly specific for kanamycin. Based on competitive direct ELISA, the detection limits of kanamycin were determined to be 1.1 ng/ml in PBS, 1.4 ng/ml in plasma, and 1.0 ng/ml in milk. The concentration of intramuscularly injected kanamycin was successfully monitored in rabbit plasma with competitive direct ELISA. Based on the colloidal gold-based immunochromatographic assay, the detection limits of kanamycin were estimated to be about 6-8 ng/ml in PBS, plasma, and milk. The immunochromatographic assay would be suitable for rapid and simple screening of kanamycin residues in veterinary medicine. Screened positives can be confirmed using a more sensitive laboratory method such as competitive direct ELISA. Therefore, the assays developed in this study could be used to complement each other as well as other laboratory findings. Moreover, instead of slaughtering the animals to obtain test samples, these methods could be applied to determine kanamycin concentration in the plasma of live animals.