Hou Jun, Zhang Jian, Liu Jia, Zhao Jing, Guo Jing-Xia, Cheng Lin, Xu Jun, Liu Ai-Xia, Song Yong-Ji, Li Bo-An, Wei Hong-Shan
Medical University of PLA, Beijing 100853, China.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2013 Aug;27(4):298-300.
To establish microplate chemiluminescence enzyme immunoassay (CLEIA) for quantitative analysis of tissue inhibitor of metalloproteinases I (TIMP I) in human serum.
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.
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.
Established CLEIA for quantity determination of serum TIMP I has high accuracy, sensitivity and repeatability.
建立微孔板化学发光酶免疫分析法(CLEIA)用于定量检测人血清中基质金属蛋白酶组织抑制因子I(TIMP I)。
以辣根过氧化物酶(HRP)标记的TIMP I单克隆抗体为催化酶,H2O2 - 鲁米诺为发光试剂进行夹心反应。研究并优化了免疫反应条件、TIMP I - HRP稀释比例、发光反应时间等多个理化参数。为评估该方法,进行了回收率试验、热稳定性试验和对比试验。
线性范围为0.2 - 12 ng/ml,r = 0.996。检测限为0.12 ng/ml。批间和批内相对标准偏差均小于10%。三个不同加标浓度样品的回收率分别为100.6%、96.5%和106.5%。在4℃和37℃分别保存3、5、7天后,分析显示相关系数高于0.998,相对标准偏差低于6%。在60例肝纤维化患者血清中,CLEIA检测结果与进口ELISA检测结果高度吻合。
建立的用于血清TIMP I定量测定的CLEIA具有高准确性、高灵敏度和高重复性。