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作 者:王迪[1] 杨曙明[1] 张波 宋荣[1] 熊勇华 于洪侠[1] 杨晓慧
机构地区:[1]中国农业科学院农业质量标准与检测技术研究所,北京100081 [2]北京中德大地食品安全技术开发有限公司
出 处:《分析科学学报》2007年第6期665-668,共4页Journal of Analytical Science
基 金:农业部948项目(2003-Q08)
摘 要:以单抗为配基制备克仑特罗免疫亲和柱,建立了简单、快速、特异的样品净化技术,柱容量达到100 ng。偶联抗体量与柱容量呈线性关系,线性方程为:y=236.36x+6.6214,R2=0.9461。测定尿样中的克仑特罗,不需前处理直接用亲和柱提纯后以气质联用(GC/MS)方法检测。空白猪尿添加浓度为205、01、00 ng时,回收率分别为85%±1.3,85.9%±1.3,81.5%±2.7。同时以NY/XQ421-2003标准中净化方法为对照,回收率分别为113%±5.6,94.5%±10,78.6%±1.7,偶联非特异抗体的对照组亲和柱对样品保留值为7.03%。数据显示:免疫亲和柱作为提纯方法,与传统固相萃取提纯方法相比平行性好,提纯后样本杂质少。因此免疫亲和柱是净化样品的一个有效方法。A simple, rapid and specific preparative method was developed, which was based on monoclonal antibody-mediated immunoaffinity column (IAC) for clenbuterol. The dynamic column capacity was more than 100 ng , which is related with the antibody quantity, and the regression equation was y= 236. 36x + 6. 6214,R^2= 0. 9461.Urine sample could be directely applied to immunoaffinity column before determination by GC/MS without any other pretreatments. The recoveries of blank pig urine fortified samples at levels of 20 ng/mL,50 ng/mL and 100 ng/mL were 85%±1.3,85.9%±1.3 and 81.5%±2.7. At the same time, to treat the fortified urine samples by the standard method of NY/XQ421-2003, the recoveries were 113%±5.6,94.5%±10 and 78.6%±1.7. A control column prepared from nonspecific IgG retained 7. 03%. The results showed that compared to traditional solid phase extraction (SPE) cleanup method, IAC has a better parallelism and reduces more impurities which facilitates immunoaffinity chromatography to be an efficient cleanup method.
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