Department of BioNano Technology, Gachon University, 1342 Seongnamdae-ro, Sujeong-gu, Seongnam 13120, Republic of Korea.
Division of Research and Development Equipment Industry, Center for Scientific Instrumentation, Korea Basic Science Institute, 169-148 Gwahak-ro, Yuseong-gu, Daejeon 34133, Republic of Korea.
Biosensors (Basel). 2024 Apr 10;14(4):185. doi: 10.3390/bios14040185.
As a potent detection method for cancer biomarkers in physiological fluid, a colorimetric and electrochemical dual-mode sensing platform for breast cancer biomarker thioredoxin 1 (TRX1) was developed based on the excellent peroxidase-mimicking and electrocatalytic property of Prussian blue nanoparticles (PBNPs). PBNPs were hydrothermally synthesized using K[Fe(CN)] as a precursor and polyvinylpyrrolidone (PVP) as a capping agent. The synthesized spherical PBNPs showed a significant peroxidase-like activity, having approximately 20 and 60% lower values for 3,3',5,5'-tetramethylbenzidine (TMB) and HO, respectively, compared to those of horseradish peroxidase (HRP). The PBNPs also enhanced the electron transfer on the electrode surface. Based on the beneficial features, PBNPs were used to detect target TRX1 via sandwich-type immunoassay procedures. Using the strategies, TRX1 was selectively and sensitively detected, yielding limit of detection (LOD) values as low as 9.0 and 6.5 ng mL via colorimetric and electrochemical approaches, respectively, with a linear range of 10-50 ng mL in both strategies. The PBNP-based TRX1 immunoassays also exhibited a high degree of precision when applied to real human serum samples, demonstrating significant potentials to replace conventional HRP-based immunoassay systems into rapid, robust, reliable, and convenient dual-mode assay systems which can be widely utilized for the identification of important target molecules including cancer biomarkers.
作为一种在生理流体中检测癌症生物标志物的有效方法,基于普鲁士蓝纳米粒子(PBNPs)优异的过氧化物酶模拟和电催化性能,开发了用于乳腺癌生物标志物硫氧还蛋白 1(TRX1)的比色和电化学双模式传感平台。PBNPs 是用水热法使用 K[Fe(CN)]作为前体和聚乙烯吡咯烷酮(PVP)作为封端剂合成的。合成的球形 PBNPs 表现出显著的过氧化物酶样活性,对于 3,3',5,5'-四甲基联苯胺(TMB)和 HO,分别具有约 20%和 60%的低值,与辣根过氧化物酶(HRP)相比。PBNPs 还增强了电极表面的电子转移。基于有益的特性,PBNPs 被用于通过三明治型免疫测定程序检测靶标 TRX1。使用这些策略,可以选择性和灵敏地检测 TRX1,通过比色和电化学方法分别获得低至 9.0 和 6.5 ng mL 的检测限(LOD)值,两种策略的线性范围均为 10-50 ng mL。基于 PBNP 的 TRX1 免疫测定法在应用于真实的人血清样本时也表现出高度的精度,这表明它们有潜力取代传统的基于 HRP 的免疫测定系统,成为快速、稳健、可靠和方便的双模式测定系统,可广泛用于鉴定包括癌症生物标志物在内的重要靶标分子。