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   <subfield code="a">Enzyme-linked immunosorbent assay and colloidal gold-based immunochromatographic assay for several (fluoro)quinolones in milk</subfield>
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   <subfield code="c">[Wei Sheng, Yuanzhen Li, Xin Xu, Meng Yuan, Shuo Wang]</subfield>
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   <subfield code="a">We have developed a heterologous direct competitive enzyme-linked immunosorbent assay (ELISA) and a visual colloidal gold-based immunochromatographic assay (CGIA) for simultaneous determination of ofloxacin, marbofloxacin, and fleroxacin residues in milk using polyclonal antibodies. The half-maximum inhibition concentrations (IC50) of ofloxacin, marbofloxacin, fleroxacin, and limits of detection (LODs; calculated as IC15 values) are between 0.20 and 0.53ng mL−1, and between 0.02 and 0.05ng mL−1, respectively. The average recoveries range from of 78% to 113%, and the coefficients of variation of intra- and inter-assays are between 2 and 11%, and 3 to 19%, respectively. The LODs for ofloxacin, marbofloxacin, fleroxacin in milk are between 3.5 and 8.9ng mL−1. The visual minimum detection limit of the optimized CGIA is 2ng mL−1 for milk samples. The detection process can be completed within 10min. The strips can be stored at 4°C for 8weeks without significant loss of activity. The results of the analysis of spiked samples showed that the CGIA can be applied to preliminary, fast, and on-site screening of milk samples. The ELISA and CGIA allow for a rapid, sensitive, and low-cost determination of (fluoro)quinolones residues in milk samples. Figure A direct competitive enzyme-linked immunosorbent assay (ELISA) and a visual colloidal gold-based immunochromatographic assay (CGIA) are proposed for simultaneous determination of ofloxacin, marbofloxacin, and fleroxacin residues in milk using polyclonal antibodies</subfield>
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