[微孔板化学发光酶免疫分析法用于金属蛋白酶组织抑制剂的定量分析]。

中华实验和临床病毒学杂志 Pub Date : 2013-08-01
Jun Hou, Jian Zhang, Jia Liu, Jing Zhao, Jing-Xia Guo, Lin Cheng, Jun Xu, Ai-Xia Liu, Yong-Ji Song, Bo-An Li, Hong-Shan Wei
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引用次数: 0

摘要

目的:建立微孔板化学发光酶免疫分析法(CLEIA)定量分析人血清中组织金属蛋白酶抑制剂I (TIMP I)的方法。方法:以辣根过氧化物酶(HRP)标记的TIMP I单克隆抗体为催化酶,以h2o2 -鲁米诺为发光试剂,进行夹心反应。对免疫反应条件、TIMP I-HRP稀释比、发光反应时间等理化参数进行了研究和优化。为了对该方法进行评价,进行了回收试验、热稳定性试验和对比试验。结果:线性范围为0。2 ~ 12 ng/ml, r = 0.996。检出限为0.12 ng/ml。组间和组内RSD均小于10%。三种不同加标浓度样品的加标回收率分别为100.6%、96.5%和106.5%。在4℃和37℃条件下贮藏3、5、7 d后,相关系数均大于0。RSD < 6%。60例肝纤维化患者血清CLEIA检测结果与进口ELISA检测结果基本一致。结论:建立的CLEIA法测定血清中TIMP - 1含量具有较高的准确性、灵敏度和重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Microplate chemiluminescence enzyme immunoassay for the quantitative analysis of tissue inhibitor of metalloproteinases I].

Objective: To establish microplate chemiluminescence enzyme immunoassay (CLEIA) for quantitative analysis of tissue inhibitor of metalloproteinases I (TIMP I) in human serum.

Methods: A sandwich reaction was preformed with horseradish peroxidase(HRP) labeled monoclonal antibody of TIMP I as the catalytic enzyme and the H2O2-luminol as the luminescence reagent. Several physical and chemical parameters were studied and optimized such as immunoreaction conditions, the dilution ratio of TIMP I-HRP, luminescence reaction time and so on. In order to evaluate the method, recovery test, heat stabilization test and comparison test were carried out.

Results: The linear range was 0. 2-12 ng/ml with r = 0.996. The detection limit was 0.12 ng/ml. Inter-assay and intra-assay RSD were both less than 10%. The recoveries of three different spiked concentration samples were 100.6%, 96.5% and 106.5%. After stored at 4 degrees C and 37 degrees C for 3, 5, 7 days, the analysis showed correlation coefficient higher than 0. 998 and RSD lower than 6%. The detected results with CLEIA closely corresponded to those with imported ELISA in 60 patients sera with liver fibrosis.

Conclusion: Established CLEIA for quantity determination of serum TIMP I has high accuracy, sensitivity and repeatability.

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