Division of Applied Life Science (BK 21 program), Graduate School, Institute of Agriculture and Life Science, Gyeongsang National University, Chinju, Gyeongnam 660-701, Korea.
J Agric Food Chem. 2009 May 27;57(10):4035-41. doi: 10.1021/jf900075h. Epub 2009 Apr 6.
A monoclonal antibody (mAb)-based gold nanoparticle immunochromatographic assay (ICG) for zearalenone detection was developed, optimized, and validated. The detection limits of ICG optimized with appropriate amounts of zearalenone-bovine serum albumin and gold nanoparticle-mAb to zearalenone were 2.5 ng/mL and 30 μg/kg for the standard solution and spike sample, respectively, and a weak cross-reaction for α-zearalenol and β-zearalenol was observed. The assay required only 15 min to obtain results and one step to perform the assay. In validation, the results obtained from spiked corn (10, 20, 30, 50, and 100 μg/kg) and naturally contaminated corn samples by the ICG were in good agreement with those obtained by direct competitive enzyme-linked immunosorbent assay (DC-ELISA) and high-performance liquid chromatography (HPLC). Therefore, the results obtained in this study could be used as basic research for the development of zearalenone-ICG, and the ICG developed could be a useful on-site screening tool for the rapid detection of zearalenone in corn without special instrumentation.
建立、优化和验证了一种基于单克隆抗体(mAb)的金纳米粒子免疫层析检测法(ICG)用于检测玉米赤霉烯酮。通过优化金纳米粒子-mAb 与玉米赤霉烯酮-牛血清白蛋白的适当比例,ICG 的检测限在标准溶液和加标样品中分别为 2.5ng/mL 和 30μg/kg,并且对α-玉米赤霉烯醇和β-玉米赤霉烯醇表现出较弱的交叉反应性。该检测法仅需 15 分钟即可获得结果,且仅需一步即可完成检测。在验证中,ICG 对添加(10、20、30、50 和 100μg/kg)和自然污染玉米样品中玉米赤霉烯酮的检测结果与直接竞争酶联免疫吸附测定法(DC-ELISA)和高效液相色谱法(HPLC)的检测结果一致。因此,本研究中的结果可作为开发玉米赤霉烯酮-ICG 的基础研究,并且开发的 ICG 可以作为一种无需特殊仪器的快速检测玉米中玉米赤霉烯酮的现场筛选工具。