Department of Medical Engineering, Graduate School, Kyung Hee University, Seoul 130-701, Korea.
Department of Biomedical Engineering, College of Medicine, Kyung Hee University, Seoul 130-701, Korea.
Sensors (Basel). 2018 May 24;18(6):1685. doi: 10.3390/s18061685.
Detection of salivary pepsin has been given attention as a new diagnostic tool for laryngopharyngeal reflux (LPR) disease, because saliva collection is non-invasive and relatively comfortable. In this study, we prepared polypyrrole nanocorals (PPNCs) on a screen-printed carbon electrode (SPCE) by a soft template synthesis method, using β-naphthalenesulfonic acid (NSA) (for short, PPNCs/SPCE). Gold nanoparticles (GNPs) were then decorated on PPNCs/SPCE by electrodeposition (for short, GNP/PPNCs/SPCE). To construct the immunosensor, pepsin antibody was immobilized on GNP/PPNCs/SPCE. Next, citric acid was applied to prevent non-specific binding and change the electrode surface charge before pepsin incubation. Electrochemical stepwise characterization was performed using cyclic voltammetry, and immunosensor response toward different pepsin concentrations was measured by differential pulsed voltammetry. As a result, our electrochemical immunosensor showed a sensitive detection performance toward pepsin with a linear range from 6.25 to 100 ng/mL and high specificity toward pepsin, as well as a low limit of detection of 2.2 ng/mL. Finally, we quantified the pepsin levels in saliva samples of LPR patients ( = 2), showing that the results were concordant with those of a conventional ELISA method. Therefore, we expect that this electrochemical immunosensor could be helpful for preliminarily diagnosing LPR through the detection of pepsin in saliva.
唾液胃蛋白酶的检测已作为一种新的诊断工具用于喉咽反流(LPR)疾病,因为唾液采集是非侵入性的,相对舒适。在这项研究中,我们通过软模板合成方法在丝网印刷碳电极(SPCE)上制备了聚吡咯纳米珊瑚(PPNCs),使用β-萘磺酸(NSA)(简称 PPNCs/SPCE)。然后通过电沉积在 PPNCs/SPCE 上修饰金纳米颗粒(GNPs)(简称 GNP/PPNCs/SPCE)。为了构建免疫传感器,将胃蛋白酶抗体固定在 GNP/PPNCs/SPCE 上。接下来,应用柠檬酸在胃蛋白酶孵育前防止非特异性结合并改变电极表面电荷。使用循环伏安法进行电化学逐步表征,并通过差分脉冲伏安法测量针对不同胃蛋白酶浓度的免疫传感器响应。结果,我们的电化学免疫传感器对胃蛋白酶表现出灵敏的检测性能,线性范围为 6.25 至 100 ng/mL,对胃蛋白酶具有高特异性,检测限低至 2.2 ng/mL。最后,我们定量了 LPR 患者唾液样本中的胃蛋白酶水平(n=2),结果与传统 ELISA 方法的结果一致。因此,我们期望这种电化学免疫传感器可以通过检测唾液中的胃蛋白酶来帮助初步诊断 LPR。