Quantitative and rapid detection of C-reactive protein using quantum dot-based lateral flow test strip

被引:71
|
作者
Wu, Ruili [1 ]
Zhou, Shuai [2 ]
Chen, Ting [2 ]
Li, Jinjie [1 ]
Shen, Huaibin [1 ]
Chai, Yujuan [2 ]
Li, Lin Song [1 ]
机构
[1] Henan Univ, Key Lab Special Funct Mat, Minist Educ, Kaifeng 475004, Henan, Peoples R China
[2] NepQD Biotech Corp, Taizhou 225300, Peoples R China
基金
中国国家自然科学基金;
关键词
C-reactive protein; Quantum dots; QD-based lateral flow immunoassays; SENSITIVE DETECTION; IMMUNOCHROMATOGRAPHIC ASSAY; IMMUNOASSAY; LABELS;
D O I
10.1016/j.aca.2017.12.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel QD-based immunoassay on a paper-based lateral flow system has been developed to quantitatively detect C-reactive protein (CRP). Different standard CRP antigens from 1 to 200 mu g mL(-1) were diluted 200-fold and only 60 mu L diluted sample were needed to load onto the sample pad. The QD fluorescence signals on the test line and the control line were able to be observed within 3 min after the initiation of assay, and the limit of detection was as sensitive as 0.30 ng mL(-1) by measuring the fluorescence intensity immediately afterwards with fluorescence immunoassay analyzer. The linearity on the detection of QD fluorescence signals has been established well in the range of 0.5 ng mL(-1) and 1 mu g mL(-1) for CRP. The precision of the assay has been confirmed for low coefficient of variation (CV), satisfying less than 15% (intra-assay and inter-assay), and the accuracy of assay meets the requirements with the mean recovery of the control was 102.63%. These results indicated that such newly developed platform was reliable with high sensitivity, rapidness, and could cover a broad range of target concentrations. Furthermore, a total of 135 human serum clinical samples with inflammation or infection with the concentration of CRP from 0.2 to 200 mu g mL(-1) has been used to check the performance of this QD-based LFIA, it correlated very well with Roche Tina-quant CRP (Latex) (r = 0.966, n = 135). (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 7
页数:7
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