Kim So Eun, Sankar Kathannan, Yoon Jae Chol, Muthurasu Alagan, Kim Hak Yong
Research Institute of Clinical Medicine of Jeonbuk National University and Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju 54907, South Korea.
Division of Animal Disease and Health, National Institute of Animal Science, Rural Development Administration, Wanju 55365, Republic of Korea.
ACS Appl Bio Mater. 2025 May 19;8(5):4153-4165. doi: 10.1021/acsabm.5c00276. Epub 2025 Apr 14.
An electrochemical sandwich immunoassay was fabricated to measure the prostate-specific antigen (PSA) biomarker. The PSA immunosensor was developed by altering the surface of a glassy carbon electrode (GCE) with a nanocomposite comprising carboxyl-functionalized carbon dots that support gold nanoparticles (AuNPs), which were then combined with hydroxylated boron nitride nanosheets (HO-BN). This construction possesses distinctive signal enhancement characteristics and was prepared via a facile method. Considering the high biological affinity of AuNPs for biomolecules, carbon dots (CDs) with carboxyl (COOH) groups make a suitable substrate for electrode modification. This alteration allows for the PSA antibody (Ab1) attachment, resulting in a sandwich-like configuration. Additionally, carbon dot-stabilized AuNPs integrated into HO-BN nanosheet nanocomposites considerably boost the electron transfer rate, leading to remarkable potential in sensor applications. By utilizing horseradish peroxidase (HRP)-conjugated antifree PSA antibody (Ab2), a reduction in hydrogen peroxide (HO) was achieved within the electrochemical cell. This reduction led to increased current, attributed to the increased PSA concentration, which is required for the biosensor analysis to perform properly. The developed immunosensor revealed a linear correlation with PSA concentrations ranging from 1.0 to 3500 pg mL, achieving a low detection limit of 0.136 pg mL. Furthermore, the PSA aptasensor demonstrates excellent selectivity, remarkable stability, and commendable reproducibility, indicating its significant potential for clinical research and diagnostic applications.
构建了一种电化学夹心免疫分析法来检测前列腺特异性抗原(PSA)生物标志物。通过用包含支撑金纳米颗粒(AuNPs)的羧基功能化碳点的纳米复合材料改变玻碳电极(GCE)的表面来开发PSA免疫传感器,然后将其与羟基化氮化硼纳米片(HO-BN)结合。这种结构具有独特的信号增强特性,并且通过简便的方法制备。考虑到AuNPs对生物分子具有高生物亲和力,带有羧基(COOH)基团的碳点(CDs)成为电极修饰的合适底物。这种改变允许PSA抗体(Ab1)附着,从而形成夹心状结构。此外,整合到HO-BN纳米片纳米复合材料中的碳点稳定的AuNPs大大提高了电子转移速率,在传感器应用中具有显著潜力。通过使用辣根过氧化物酶(HRP)偶联的抗游离PSA抗体(Ab2),在电化学池中实现了过氧化氢(HO)的还原。这种还原导致电流增加,这归因于PSA浓度的增加,而这是生物传感器分析正常运行所必需的。所开发的免疫传感器与PSA浓度在1.0至3500 pg/mL范围内呈线性相关,实现了0.136 pg/mL的低检测限。此外,PSA适体传感器表现出优异的选择性、显著的稳定性和良好的重现性,表明其在临床研究和诊断应用中具有巨大潜力。