生物技术通报 ›› 2017, Vol. 33 ›› Issue (3): 199-204.doi: 10.13560/j.cnki.biotech.bull.1985.2017.03.029

• 研究报告 • 上一篇    下一篇

尿微量白蛋白荧光免疫层析定量检测试剂的研制及性能评价

张赛1, 洪裕好1, 李凯1, 何小维2, 李文美1,2   

  1. 1. 广州万孚生物技术股份有限公司 自检型快速诊断国家地方联合工程实验室,广州 510663;
    2. 华南理工大学食品科学与工程学院,广州 510640
  • 收稿日期:2016-09-09 出版日期:2017-03-26 发布日期:2017-03-07
  • 作者简介:张赛,男,硕士研究生,研究方向:免疫检测技术;E-mail:zhangsai0623@126.com
  • 基金资助:
    国家科技支撑计划资助项目(2012BAI19B05),广州市科技计划资助项目(201503020003)

Establishment and Performance Evaluation of a Quantitative Detection Method for Microalbuminuria Based on Fluorescence Immunochromatography

ZHANG Sai1, HONG Yu-hao1, LI Kai1, HE Xiao-wei2, LI Wen-mei1,2   

  1. 1. National & Local United Engineering Lab of Rapid Diagnostic Test,Wondfo Biotech Co.,Ltd.,Guangzhou 510663;
    2. College of Food Science and Engineering,South China University of Technology,Guangzhou 510640
  • Received:2016-09-09 Published:2017-03-26 Online:2017-03-07

摘要: 旨在建立一种快速定量检测人尿液中微量白蛋白的荧光免疫层析方法。以羧基荧光微球标记的抗人白蛋白单克隆抗体及羊抗兔IgG为标记抗体,人白蛋白和兔IgG分别作为检测线和质控线制备荧光免疫层析试纸条。结果显示,所制备检测试剂的线性范围为5-300 mg/L,检测限为2.3 mg/L,批内和批间变异系数(CV)分别为6.4%-9.3%和6.5%-12.3%,平均回收率为102.3%。试剂与尿液中20种干扰物质无交叉反应,实时稳定性试验表明试剂盒有效期>12月。临床样本测试,与Orion QuikRead U-ALB试剂相关性较好(r=0.993,P<0.01),Bland-Altman分析表明两种方法的诊断结果具有较好的一致性。所制备的荧光免疫层析检测试剂提供了一种简单、快速、准确的定量检测尿液中微量白蛋白的方法。

关键词: 尿微量白蛋白, 荧光免疫层析, 快速检测

Abstract: This work aims to develop a rapid quantitative detecting method of fluorescence immunochromatographic assay(FICA)for human urinary microalbuminuria(MAU). The fluorescence immunochromatographic strips were successfully prepared with anti-human albumin monoclonal antibody and goat anti-rabbit IgG marked by carboxyl fluorescent microspheres as the detection antibody,human albumin as the test line,and the rabbit IgG as the control line. As the results showed,the linear range of prepared kit(i.e.,fluorescence immunochromatographic strips)was in 5 mg/L-300 mg/L with a detection limit of 2.3 mg/L. The intra- and inter-assay coefficient of variation was 6.4%-9.3% and 6.5%-12.3%,respectively. The average recovery percent was 102.3%. The kit showed solid specificity as there was no cross-reactivity with 20 kinds of interfering substances. The shelf time of the kit by real-time stability test was > 12 months. Test with clinical urinary samples by the kit showed high correlation(r = 0.993,P < 0.01)with the control Orion QuikRead U-ALB kit,and Bland-Altman analysis showed that the diagnostic results of the two methods presented promising consistency. In conclusions,the prepared fluorescence immunochromatographic kit provides a simple,rapid and accurate quantitative detection method for microalbuminuria.

Key words: microalbuminuria, fluorescence immunochromatography, rapid detection