胶体金免疫层析技术快速定量检测金黄色葡萄球菌肠毒素B
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谢士嘉 女 学士 实习研究员 研究方向为生物快速 检测技术 E2mail: xieshijia1105@126. com

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国家十一五科技支撑计划(2006BAK10B07) ;质检公益项 目(2007GYJ023) ;国家质检总局科技计划(2006 IK165) 。


Rapid and Quantitative Detection of Staphylococcal Enterotoxin B with Colloid Gold Immunochromatography
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    摘要:

    目的 建立胶体全免疫层析技术快速定量检测金黄色葡萄球菌肠毒素B的方法.方法 利用胶体金标记和双抗体夹心免疫层析技术,建立金黄色葡萄球茵肠毒素B的快速检测方法,评价其特异性和敏感性,并拟合检测曲线进行定量检测;在牛奶样品中添加金黄色葡萄球茵肠毒素B作为模拟污染样品进行检测.结果 该法可在5~10 min内完成定性和半定量检测,检出限为8 ng/ml,线性范围8~1000 ng/ml.结论 建立的检测金黄色葡萄球菌肠毒素B的胶体金免疫层析方法,能快速、灵敏、特异、准确地检测样品中的金黄色葡萄球菌肠毒素B,并可实现定量,适用于现场快速检测.

    Abstract:

    Objective To develop a rap id method for the detection and quantification of S taphylococcal enterotoxin B ( SEB) in foods. Method Using colloid gold as a marker and utilizing double-antibody sandwich immunochromatographic assay to rap idly detect S taphylococcal enterotoxin B in foods, and to evaluate the specificity and sensitivity of the method. The quantification was realized by constructing a standard curve. The feasibility of the method was tested by adding SEB to various food samp les, such as milk powder. Results The qualitative as well as semi-quantitative detection could be comp leted in 5-10 min. The limit of detection was 8 ng/ml; the linear range was from 8 ng/ml to 1000 ng/ml. The recovery rate was 120.82% and 120.23%. The specificity and sensitivity of the method was good, and the samp les could be detected directly after simp le p rocessing. Conclusion The established colloidal gold immunochromatographic assaywas able to detect SEB in food samp les rap idly, specifically, sensitively and accurately, and was able to realize quantitative detection in the fields.

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谢士嘉 ,王 静,姜永强,张 然,杨 宇,孙肖红,胡孔新,周文君.胶体金免疫层析技术快速定量检测金黄色葡萄球菌肠毒素B[J].中国食品卫生杂志,2010,22(1):31-35.

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