The development of dual-label time-resolved fluorescence immunoassay (TRFIA) for screening of ovarian cancer based on simultaneous detection of human epididymis protein-4 and cancer antigen 125

Wengji Sun, Yan Wang, Xiao-zhu Liu, Lai-qing Li, Cuicui Chen, Licheng Zhang
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引用次数: 3

Abstract

ABSTRACT A two-step dual-label TRFIA was developed for the simultaneous detection of human epididymis protein-4 and cancer antigen 125 in a single run. The performance of this assay was first evaluated using clinical serum samples, and then compared with commercialized kits. The sensitivity of this assay for cancer antigen 125 detection was 0.5 U/mL (dynamic range, 0–1400 U/L), and the sensitivity for human epididymis protein-4 detection was 1 pM (dynamic range, 1–900 pM). High correlation coefficients (R) were obtained between the present dual-label TRFIA and commercially available kits (R = 0.99). The present dual-label TRFIA has high sensitivity, specificity, and accuracy in clinical sample analysis. It is a good alternative to the single-label diagnostic methods.
基于同时检测人附睾蛋白-4和肿瘤抗原125的双标记时间分辨荧光免疫分析法(TRFIA)用于卵巢癌筛查的研究
建立了一种两步双标记TRFIA,用于同时检测人附睾蛋白-4和癌症抗原125。首先使用临床血清样本评估该检测的性能,然后与商业化试剂盒进行比较。检测肿瘤抗原125的灵敏度为0.5 U/mL(动态范围0 ~ 1400 U/L),检测人附睾蛋白-4的灵敏度为1 pM(动态范围1 ~ 900 pM)。双标签TRFIA试剂盒与市售试剂盒具有较高的相关系数(R = 0.99)。目前的双标签TRFIA在临床样品分析中具有较高的灵敏度、特异性和准确性。这是一个很好的替代单标签诊断方法。
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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