Department of Chemistry, School of Physics and Chemistry, Gwangju Institute of Science and Technology (GIST), Gwangju 500-712, Republic of Korea.
Department of Electrical Engineering, University of California, Los Angeles, California 90095, United States.
Theranostics. 2018 May 10;8(12):3189-3197. doi: 10.7150/thno.24034. eCollection 2018.
The immunochromatographic (ICA) assay is a highly promising platform for rapid and simple detection of C-reactive protein (CRP) which is an indicator of the different phases of various diseases, as well as of inflammation and infection. However, the hook effect in the ICA assay limits the quantification of CRP levels at high CRP concentrations. In this study, we developed a hook effect-free immunochromatographic assay (HEF-ICA) to detect CRP over a wide concentration range. The hook effect results from the simultaneous reaction of an excess target antigens with both immobilized and labeled antibodies respectively. To reduce the potential occurrence of this simultaneous reaction, we separated the migration of the target antigen and gold nanoparticle (AuNP)-labeled antibodies on a nitrocellulose membrane and analyzed the time profiles by modifying the ICA structure. The signal intensity of HEF-ICA was saturated at high CRP concentrations, without decreasing. The titration curve of HEF-ICA was adjusted with the Hill equation, and HEF-ICA was performed with the following parameters: limit of detection, 43 ng mL; dynamic range, 119 ng mL to 100 µg mL. The accuracy of the newly developed assay was evaluated using 33 clinical samples via comparison with a clinical chemistry analyzer. HEF-ICA enabled the measurement of a wide range of CRP concentrations without the hook effect, and was suitable for point-of-care testing with fingertip blood sampling, as only a minute sample volume (2.5 µL) was required.
免疫层析(ICA)分析是一种很有前途的平台,可用于快速、简便地检测 C 反应蛋白(CRP),CRP 是多种疾病不同阶段的标志物,也是炎症和感染的标志物。然而,ICA 分析中的钩状效应限制了高 CRP 浓度下 CRP 水平的定量。在这项研究中,我们开发了一种无钩状效应免疫层析分析(HEF-ICA),以在宽浓度范围内检测 CRP。钩状效应是由于过量的靶抗原与固定化和标记的抗体同时反应引起的。为了减少这种同时反应的可能性,我们在硝酸纤维素膜上分别分离靶抗原和金纳米颗粒(AuNP)标记抗体的迁移,并通过修改 ICA 结构来分析时间曲线。HEF-ICA 的信号强度在高 CRP 浓度下达到饱和,而不会降低。HEF-ICA 的滴定曲线通过 Hill 方程进行调整,并且 HEF-ICA 采用以下参数进行:检测限为 43 ng mL;动态范围为 119 ng mL 至 100 µg mL。通过与临床化学分析仪比较,使用 33 个临床样本评估新开发的测定法的准确性。HEF-ICA 能够在无钩状效应的情况下测量宽范围的 CRP 浓度,并且适用于指尖采血的即时护理测试,因为仅需要微小的样本量(2.5 µL)。