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作 者:肖路延[1] 王萌[1] 朱明炜[2] 唐志毅[1] 李金明[1]
机构地区:[1]卫生部北京医院检验科,北京100730 [2]卫生部北京医院外科,北京100730
出 处:《中国临床营养杂志》2007年第2期75-78,共4页Chinese Journal of Clinical Nutrition
基 金:首都医学发展科研基金(2002-3041)
摘 要:目的采用电化学发光法测定血清叶酸含量。方法以三联吡啶钌作标记物,包被叶酸结合蛋白,待测标本中的叶酸与标记叶酸竞争性结合包被好的叶酸结合蛋白,通过外加电场的作用产生化学发光反应,即可测定出血清中叶酸的含量,并将此法测得的结果与放射免疫法测得的结果进行比较分析。结果本法线性范围为1.21~38.80nmol/L,批內和批间的变异系数分别为1.5%和2.4%,回收率为102%。本实验室血清叶酸正常参考值范围为6.2~37.6nmol/L。本法测得的血清叶酸结果与放射免疫法结果比较相关性良好(r=0.97),两种方法测定结果差异无显著性。结论电化学发光法操作简便、灵敏度高、特异性强,结果准确、可靠,适用于临床有关血清叶酸的常规检测和临床研究。Objective To determine the serum folate with electrochemiluminescence immunoassay (ECLIA). Methods After the serum folate was tied with the ruthenium-labeled folate-binding protein, we supplied a voltage to the electrode and induced chemiluminescent emission. The results were measured by a photomultiplier, and thus the serum folate was determined. ECLIA results were compared with those of radioimmunoassay (RIA). Results The linear range of ECLIA was 1.21-38.80 nmol/L, and the intra-batch and inter-batch variance coefficiency was 1.5% and 2.4% , respectively. The recovery of folate added to serum sample was 102%. The results determined with ECLIA or RIA had no significant difference. The results were also positively correlated ( r = 0. 97). Conclusion ECLIA is an accurate, rapid, specific, and suitable approach to measurement serum folate in clinical practice.
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