Research Center of Analytical Instrumentation, Key Laboratory of Bio-resource and Eco-environment, Ministry of Education, College of Life Science, Sichuan University, Chengdu, 610065, Sichuan, People's Republic of China.
Research Center of Analytical Instrumentation, School of Mechanical Engineering, Sichuan University, Chengdu, 610065, China.
Biosens Bioelectron. 2022 Apr 1;201:113911. doi: 10.1016/j.bios.2021.113911. Epub 2021 Dec 24.
The development of rapid and sensitive detection methods for pathogenic bacteria is crucial for the therapy and prevention of related diseases. However, the rapid and ultrasensitive assays are difficult to be realized simultaneously. To solve the problem, a sandwich method based on Ω-shaped fiber optic localized surface resonance (Ω-FOLSPR) was constructed, where poly adenine-tailed aptamer (PolyA-apt) and SH modified gold nanoparticles tags (AuNPs tags) were chosen as the capturing aptamer and amplifying tags, respectively. The small AuNPs were modified on the surface of fiber-optic (FO) rapidly, which saved the preparation time. Then, the PolyA-apt was modified on the AuNPs surface to capture the bacteria effectively due to its ability to adjust the density and conformation of aptamer on the AuNPs surface. Finally, the large AuNPs tags were used to generate intense signal enhancement. It is found that the sandwich method enables the unique characteristic of a time-dependent sensitivity enhancement. Specifically, the LOD of 108.0 CFU/mL and 7.4 CFU/mL was achieved with the analysis time of 10 min and 100 min, respectively. Besides, the Ω-FOLSPR sensor exhibits excellent selectivity against the other bacteria and good performance for detecting the spiked and natural samples. This sandwich method provides a time-flexible strategy due to the combination of effective signal amplification and real-time analysis for bacterial detection, displaying great potential for practical bacterial detection.
快速灵敏的致病菌检测方法的发展对于相关疾病的治疗和预防至关重要。然而,快速和超灵敏的检测方法很难同时实现。为了解决这个问题,构建了一种基于 Ω 型光纤局域表面等离激元(Ω-FOLSPR)的三明治方法,其中聚腺嘌呤尾亲和体(PolyA-apt)和 SH 修饰的金纳米粒子标签(AuNPs tags)分别被选择为捕获亲和体和放大标签。小的 AuNPs 被快速修饰在光纤(FO)表面上,从而节省了制备时间。然后,由于其能够调节 AuNPs 表面上的亲和体的密度和构象,PolyA-apt 被修饰在 AuNPs 表面上以有效捕获细菌。最后,大的 AuNPs 标签被用于产生强烈的信号增强。结果发现,三明治方法能够产生依赖时间的灵敏度增强的独特特性。具体而言,在 10 分钟和 100 分钟的分析时间下,分别实现了 108.0 CFU/mL 和 7.4 CFU/mL 的检测限。此外,该 Ω-FOLSPR 传感器对其他细菌具有出色的选择性,并且对检测添加和自然样品具有良好的性能。这种三明治方法由于有效信号放大和实时分析的结合,为细菌检测提供了一种灵活的时间策略,显示出在实际细菌检测中具有很大的潜力。