Lv Ke, Wang Weitao, Zhang Li, Zhou Xi, Yu Hongyan, Han Xiaole, Wang Li, Xie Guoming, Yang Gang
Department of Neurosurgery, The First Affiliated Hospital of Chongqing Medical University, No.1 Youyi Road, Chongqing, 40016, People's Republic of China.
Key Laboratory of Clinical Laboratory Diagnostics (Chinese Ministry of Education), College of Laboratory Medicine, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
Anal Sci. 2025 Jul 22. doi: 10.1007/s44211-025-00826-5.
Fibrinogen is a vital biomarker for coagulation disorders, with reduced levels increasing bleeding risk and mortality, requiring rapid detection for early diagnosis. Enzyme-linked immunosorbent assay (ELISA) is commonly employed in clinical environments; however, its prolonged processing duration and insufficient sensitivity hinder its utility for swift diagnostics. We addressed these limitations by creating a dual-antibody sandwich immunoassay that employs upconversion nanoparticles (UCNPs) and magnetic beads (MBs) for the precise and sensitive detection of fibrinogen. The enhanced analytical performance of the method is attributed to the use of UCNPs and MBs. UCNPs enhance the signal-to-noise ratio by emitting visible light under near-infrared excitation, which reduces background interference from autofluorescence and light scattering in biological samples. Meanwhile, MBs facilitate specific enrichment of fibrinogen by selectively capturing the target analyte, enabling efficient isolation from complex sample matrices. This synergy improves sensitivity and specificity, achieving a 2 ng/mL detection limit with a 15-fold sensitivity increase, simpler operation, and shorter detection time compared to conventional ELISA kits. This platform offers a robust solution for fibrinogen detection, with potential for broad application in clinical diagnostics.
纤维蛋白原是凝血障碍的重要生物标志物,其水平降低会增加出血风险和死亡率,需要进行快速检测以实现早期诊断。酶联免疫吸附测定(ELISA)在临床环境中常用;然而,其较长的处理时间和不足的灵敏度阻碍了它在快速诊断中的应用。我们通过创建一种双抗体夹心免疫测定法解决了这些局限性,该方法采用上转换纳米颗粒(UCNPs)和磁珠(MBs)来精确灵敏地检测纤维蛋白原。该方法增强的分析性能归因于UCNPs和MBs的使用。UCNPs通过在近红外激发下发射可见光来提高信噪比,这减少了生物样品中自发荧光和光散射的背景干扰。同时,MBs通过选择性捕获目标分析物促进纤维蛋白原的特异性富集,从而能够从复杂的样品基质中有效分离。这种协同作用提高了灵敏度和特异性,实现了2 ng/mL的检测限,与传统ELISA试剂盒相比灵敏度提高了15倍,操作更简单,检测时间更短。该平台为纤维蛋白原检测提供了强大的解决方案,在临床诊断中具有广泛应用的潜力。