Evaluation of a magnetic particles-based chemiluminescence enzyme immunoassay for Golgi protein 73 in human serum

被引:14
作者
Liu, Xiangyi [1 ]
Wan, Xiaohua [1 ]
Lu, Sheng [2 ]
Zhang, Lijun [3 ]
Yu, Shaohua [4 ]
Lu, Xinxin [1 ]
机构
[1] Capital Med Univ, Beijing Tongren Hosp, Dept Lab Med, Beijing 100730, Peoples R China
[2] Beijing Ranos Med Technol Co Ltd, Beijing, Peoples R China
[3] Capital Med Univ, Beijing Tongren Hosp, Dept Surg, Beijing 100730, Peoples R China
[4] Beijing Hotgen Biotechnol Co Ltd, Beijing, Peoples R China
关键词
Golgi protein 73; Chemiluminescence enzyme immunoassay; Evaluation; Magnetic particles; Hepatocellular carcinoma; ALPHA-FETOPROTEIN AFP; HEPATOCELLULAR-CARCINOMA; LIVER-DISEASES; GP73; MARKER; EXPRESSION; DIAGNOSIS; ANTIGEN; GOLPH2; SYSTEM;
D O I
10.1016/j.cca.2015.03.008
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Golgi protein 73 (GP73) is regarded as a potential serum biomarker for early diagnosis of hepatocellular carcinoma (HCC). We developed a rapid magnetic particles-based chemiluminescence enzyme immunoassay (MPs-CLEIA) for the determination of serum GP73. Methods: Fluorescein isothiocyanate (FITC) and alkaline phosphatase (ALP) were used to label 2 different monoclonal antibodies to GP73. Serum GP73 was captured with labeled antibodies and formed a sandwiched immunoreaction. The magnetic particles (MPs) coated with anti-FITC antibody were used as a means of separation of the GP73 protein from other serum proteins. After adding the enzyme substrate solution, the relative light unit (RLU) was measured. A MPs-CLEIA for serum GP73 was established and evaluated. Results: The RLU was directly proportional to the concentration of GP73. The method linearity was 5-600 mu g/I. Limit of the blank was 2.19 mu g/I. The intra- and inter-assay imprecision was <3% and <5%, respectively. The average recoveries were between 95% and 105%. The proposed method showed a good correlation with a commercial ELISA assay (r = 0.983, p < 0.001). We also evaluated the efficiency of serum GP73 measurement for the diagnosis of HCC using this assay. The area under the receiver operating characteristic curve was 0.822 (95% CI, 0.73-0.89), and the sensitivity and specificity, with cut-off value of 115.6 mu g/I, were 75.4% and 92.1%, respectively. Conclusions: The proposed method demonstrates an acceptable performance for quantifying serum GP73. This assay could be appropriate for routine use in clinical laboratories. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 59
页数:6
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