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作 者:何俊[1] 李勇[1] 但德忠[2] 李毓琦[1] 乔小蓉[1] 王方强[2]
机构地区:[1]四川大学华西医学中心药学院,四川成都610041 [2]四川大学环境科学与工程学院,四川成都610056
出 处:《分析测试学报》2001年第5期31-33,共3页Journal of Instrumental Analysis
基 金:国家自然科学基金资助项目 (39570218)
摘 要:用新型荧光光纤免疫传感流动分析测试系统 ,对人血清白蛋白 (HSA)进行测试 ;将偶联于微晶纤维素表面形成的HSA固相抗体与待测HSA(抗原 )、荧光标记抗原 (FITC_HSA)竞争性结合 ,经稀碱液处理 ,固相载体与抗原抗体复合物分离 ,用新型荧光光纤免疫传感流动分析系统测定解析液的荧光值 ,以求得待测HSA的含量 ;该法检出限为0.1g/L ,日内RSD0.91 %~6.4 % ,日间RSD1.8 %~8.0 %,加标回收率91 %~120 % ;用该法测定注射用HSA,与临床检验常用的溴甲酚绿法对照,具有良好的相关性 (r=0.9808)。A novel flow _ injection fluorescence immunoassay system with fiber _ optic sensor has been developed for the determination of human serum albumin(HSA). A solid phase antibody of HSA was prepared by linking HSA antibody to microcrystalline cellulose, then to it HSA and labeling HSA with a fluorescent tag were competitively bonded. The formed antigen-antibody complex was dealt with a dilute alkaline solution and separated from the solid support, the fluorescence yield was determined by the sys_tem. The experimental conditions were optimized. The detection limit of 0.1 g/L for HSA, intra _ day determinarion RSD of 0.91%~6.4%, inter _ day determination RSD of 1.8%~8.0% and recovery rate of 91%~120% were found. The analytical results of HSA obtained by proposed method were well related to those of clinical bromcresol green(BCG) method(r=0.980 8).em.Theexperimentalconditionswereoptimized.Thedetectionlimitof0.1g/LforHSA,intra_daydeterminarionRSDof0.91 %~6.4%,inter_daydeterminationRSDof1.8 %~8.0%andrecoveryrateof91 %~120 %werefound.TheanalyticalresultsofHSAobtainedbyproposedmethodwerewellrelatedtothoseofclinicalbromcresolgreen(BCG)met
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