Mauriz Elba
Department of Nursing and Physiotherapy, Universidad de León, Campus de Vegazana, s/n, 24071 León, Spain.
Institute of Food Science and Technology (ICTAL), La Serna 58, 24007 León, Spain.
Biosensors (Basel). 2025 Apr 12;15(4):245. doi: 10.3390/bios15040245.
Surface plasmon resonance (SPR) aptasensors benefit from the SPR phenomenon in measuring aptamer interactions with specific targets. Integrating aptamers into SPR detection enables extensive applications in clinical analysis. Specifically, virus aptasensing platforms are highly desirable to face the ongoing challenges of virus outbreaks. This study systematically reviews the latest advances in SPR aptasensors for virus detection according to PRISMA guidelines. The literature search recovered 322 original articles from the Scopus (n = 152), Web of Science (n = 83), and PubMed (n = 87) databases. The selected articles (29) deal with the binding events between the aptamers immobilized on the sensor surface and their target molecule: virus proteins or intact viruses according to different SPR configurations. The methodological quality of each study was assessed using QUADAS-2, and a meta-analysis was conducted with the CochReview Manager (RevMan) Edition7.12.0 Data were analyzed, focusing on the types of viruses, the virus target, and the reference method. The pooled sensitivity was 1.89 (95%, CI 1.29, 2.78, I = 49%). The analysis of different types of plasmonic sensors showed the best diagnostic results with the least heterogeneity for SPR conventional configurations: 3.23 (95% CI [1.80, 5.79]; I = 0%, = 0.65). These findings show that even though plasmonic biosensors effectively analyze viruses through aptamer approaches, there are still big challenges to using them regularly for diagnostics. Practical considerations for measuring label-free interactions revealed functional capabilities, technological boundaries, and future outlooks of SPR virus aptasensing.
表面等离子体共振(SPR)适体传感器在测量适体与特定靶标的相互作用时受益于SPR现象。将适体整合到SPR检测中可在临床分析中实现广泛应用。具体而言,面对持续的病毒爆发挑战,病毒适体传感平台非常必要。本研究根据PRISMA指南系统回顾了用于病毒检测的SPR适体传感器的最新进展。文献检索从Scopus(n = 152)、Web of Science(n = 83)和PubMed(n = 87)数据库中检索到322篇原始文章。所选的29篇文章根据不同的SPR配置,探讨了固定在传感器表面的适体与其靶分子(病毒蛋白或完整病毒)之间的结合事件。使用QUADAS - 2评估每项研究的方法学质量,并使用CochReview Manager(RevMan)7.12.0版进行荟萃分析。对数据进行了分析,重点关注病毒类型、病毒靶标和参考方法。合并敏感性为1.89(95%,CI 1.29,2.78,I = 49%)。对不同类型等离子体传感器的分析表明,对于SPR传统配置,诊断结果最佳,异质性最小:3.23(95% CI [1.80, 5.79];I = 0%, = 0.65)。这些发现表明,尽管等离子体生物传感器通过适体方法能有效分析病毒,但要将其常规用于诊断仍面临巨大挑战。对无标记相互作用测量的实际考量揭示了SPR病毒适体传感的功能能力、技术界限和未来展望。