Department of Engineering Science, National Cheng Kung University, Tainan 70101, Taiwan.
Division of Nephrology, Department of Internal Medicine, National Cheng Kung University Hospital, Tainan 70101, Taiwan.
Biosensors (Basel). 2024 May 30;14(6):283. doi: 10.3390/bios14060283.
A microfluidic immuno-biosensor detection system consisting of a microfluidic spectrum chip and a micro-spectrometer detection device is presented for the rapid point-of-care (POC) detection and quantification of high-sensitivity C-reactive protein (hs-CRP) in urine. The detection process utilizes a highly specific enzyme-linked immunosorbent assay (ELISA) method, in which capture antibodies and detection antibodies are pre-deposited on the substrate of the microchip and used to form an immune complex with the target antigen. Horseradish peroxidase (HRP) is added as a marker enzyme, followed by a colorimetric reaction using 3,3',5,5'-tetramethylbenzidine (TMB). The absorbance values (a.u.) of the colorimetric reaction compounds are measured using a micro-spectrometer device and used to measure the corresponding hs-CRP concentration according to the pre-established calibration curve. It is shown that the hs-CRP concentration can be determined within 50 min. In addition, the system achieves recovery rates of 93.8-106.2% in blind water samples and 94.5-104.6% in artificial urine. The results showed that the CRP detection results of 41 urine samples from patients with chronic kidney disease (CKD) were highly consistent with the conventional homogeneous particle-enhanced turbidimetric immunoassay (PETIA) method's detection results (R = 0.9910). The experimental results showed its applicability in the detection of CRP in both urine and serum. Overall, the results indicate that the current microfluidic ELISA detection system provides an accurate and reliable method for monitoring the hs-CRP concentration in point-of-care applications.
一种由微流谱芯片和微光谱仪检测装置组成的微流控免疫生物传感器检测系统,用于快速即时检测(POC)和定量尿液中的高敏 C 反应蛋白(hs-CRP)。检测过程采用高度特异的酶联免疫吸附测定(ELISA)方法,其中捕获抗体和检测抗体预先沉积在微芯片的基质上,与靶抗原形成免疫复合物。辣根过氧化物酶(HRP)作为标记酶,随后用 3,3',5,5'-四甲基联苯胺(TMB)进行比色反应。使用微光谱仪设备测量比色反应化合物的吸光度值(a.u.),并根据预先建立的校准曲线测量相应的 hs-CRP 浓度。结果表明,hs-CRP 浓度可在 50 分钟内确定。此外,该系统在盲水样品中的回收率为 93.8-106.2%,在人工尿液中的回收率为 94.5-104.6%。结果表明,41 例慢性肾脏病(CKD)患者尿液样本的 CRP 检测结果与传统均相粒子增强浊度免疫测定(PETIA)法的检测结果高度一致(R = 0.9910)。实验结果表明,该方法在尿液和血清中 CRP 的检测中具有适用性。总的来说,结果表明,当前的微流控 ELISA 检测系统为即时检测应用中 hs-CRP 浓度的监测提供了一种准确可靠的方法。