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作 者:索明环[1] 张秀明[1] 温冬梅[1] 王伟佳[1] 李飞[1] 欧阳能良[1] 阚丽娟[1] 严海忠[1]
机构地区:[1]中山大学附属中山医院检验医学中心,广东中山528403
出 处:《现代检验医学杂志》2012年第1期104-106,109,共4页Journal of Modern Laboratory Medicine
基 金:基金项目:广东省医学科研基金课题(A2009763),中山市科技局资助课题(20091A038).
摘 要:目的探讨电化学发光免疫法检测N末端B型利钠肽原(NT—proBNP)的检测限值和功能灵敏度。方法参照美国临床和实验室标准化协会(CLSI)Ep-17A文件制备空白样品及系列低浓度样品。‘空白样品采用配套的稀释液,系列低浓度样品采用倍比稀释的方法获得。样品制备后用RocheCobasE601电化学发光免疫系统检测NT-proBNP浓度,以确定该方法的空白限、检出限和功能灵敏度。结果NT—proBNP的空白限为2.53pg/ml,检出限为7.75pg/ml,10%CV时的功能灵敏度为8.82pg/ml。结论建立了RocheCobasE601电化学发光免疫系统检测NT-proBNP的空白限、检出限和功能灵敏度,为临床诊断和治疗提供了更有价值的信息。Objective To evaluate the limits of detection and functional sensitivity of electro-chemiluminescence immunoassay in detection of NT-proBNP using Clinical and Laboratory Standards Institute(CLSI)EP-17A. Methods Blank and a serial low consistency samples were detected by Roche Cobas E601 electrochemiluminescence immunoassay system to establish the limit of blank,limit of detection and functional sensitivity of NT-proBNP. Suporting diluent was blank sample and a serial low consistency samples were abtained by dilution. Results The limit of blank and limit of detection of NT-proBNP was 2.53 pg/ml,7.75 pg/ml,respectively. The functional sensitivity was 8. 82 pg/ml. Conclusion The limit of blank,limit of detection and functional sensitivity were established successfully in laboratories, which could provide more important infor- mation for the clinical diagnosis and therapy.
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