Evaluation of a new commercial assay kit for quantification of lactate dehydrogenase isoenzyme 1 in serum.

M Panteghini, R Bonora, F Pagani
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引用次数: 0

Abstract

A new method for measuring lactate dehydrogenase (EC 1.1.1.27) isoenzyme 1 using sodium perchlorate as a chaotropic chemical selective inhibitor of all lactate dehydrogenase isoenzymes containing M-subunit was evaluated. Results with this method were precise (between-day coefficient of variation less than 9%), highly linear (coefficient of correlation = 0.9998) and correlated well with lactate dehydrogenase isoenzyme 1 as determined by the conventional immunological method (coefficient of correlation = 0.976). The reference interval for 307 healthy subjects was estimated to be 23-46 U/l (95% central range, determined non-parametrically). Being simple, convenient and amenable to automation, the method provides a substantial saving in labour and reagent costs when compared with alternative analytical approaches.

一种新型血清乳酸脱氢酶同工酶1定量测定试剂盒的评价。
采用高氯酸钠作为具有m -亚基的乳酸脱氢酶同工酶的朝向化学选择性抑制剂,建立了测定乳酸脱氢酶(EC 1.1.1.27)同工酶1的新方法。结果表明,该方法与常规免疫法测定的乳酸脱氢酶同工酶1相关性好(相关系数0.976),且准确度高(日间变异系数小于9%),线性度高(相关系数0.9998)。307名健康受试者的参考区间估计为23-46 U/l(95%中心范围,非参数确定)。与其他分析方法相比,该方法简单,方便,易于自动化,可大大节省劳动力和试剂成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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