4.4 Article

Development of ic-ELISA and lateral-flow immunochromatographic assay strip for the detection of vancomycin in raw milk and animal feed

Journal

FOOD AND AGRICULTURAL IMMUNOLOGY
Volume 28, Issue 3, Pages 414-426

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/09540105.2017.1293014

Keywords

Vancomycin; ic-ELISA; lateral-flow immunochromatographic strip; raw milk; animal feed

Funding

  1. National Natural Science Foundation of China [21522102, 21301073s]
  2. National Key RD Program [2016YFD0401101]
  3. Natural Science Foundation of Jiangsu Province
  4. MOF
  5. MOE [BE2016307, BK20150145, BX20151038, BK20140003, BE2014672, BE2013613, BE2013611]

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A highly sensitive monoclonal antibody (mAb) 3H4 against vancomycin (VAN) was prepared. Indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) and lateral-flow immunochromatographic assay (ICA) were developed based on the mAb. The 50% inhibition concentration (IC50) value and limit of detection (LOD) value of ic-ELISA method for vancomycin were 0.59 and 0.06ng/mL, and for norvancomycin were 1.51 and 0.13ng/mL under optimized conditions as pH 7.4, 0.4% (m/v) NaCl, and 5% (v/v) acetonitrile. In lateral-flow ICA, the visual limit of detection (vLOD) value and cut-off values for vancomycin were 1 and 2.5ng/mL, and for norvancomycin were 5 and 10ng/mL under optimized conditions as pH 8.6 with 1mg/mL coating antigen and 1 mu g/mL gold nanoparticle-labeled mAb. In raw milk and animal feed samples, recovery rates from ic-ELISA ranged from 89.2% to 121.6%. The vLOD and cut-off value were 5-10ng/g and 100-200g/kg, respectively. Therefore, both methods were sensitive, rapid, and effective for the on-site detection and rapid mass screening of samples.

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