Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
Nanoscale. 2014 Apr 7;6(7):3804-9. doi: 10.1039/c3nr06549a.
Here, we report a simple and ultrasensitive upconversion fluorescent strip sensor based on NaYF4:Yb,Er nanoparticles (NPs) and the lateral flow immunochromatographic assay (LFIA). Carboxyl-modified β-NaYF4:Yb,Er NPs were successfully synthesized by a facile one-pot solvothermal approach, upon further coupling with monoclonal antibody, the resultant UCNPs-antibody conjugates probes were used in LFIA and served as signal vehicles for the fluorescent reporters. V. anguillarum was used as a model analyte to demonstrate the use of this strip sensor. The limit of the detection for the fluorescent strip was determined as 10(2) CFU mL(-1), which is 100 times lower than those displayed by enzyme-linked immunosorbent assays, while the time needed for the detection was only 15 min. Furthermore, no cross-reaction with other eight pathogens was found, indicating the good specificity of the strip. This developed LFIA would offer the potential as a useful tool for the quantification of pathogens analysis in the future.
在这里,我们报告了一种基于 NaYF4:Yb,Er 纳米粒子(NPs)和横向流动免疫层析分析(LFIA)的简单、超灵敏的上转换荧光条传感器。通过简便的一锅溶剂热方法成功合成了羧基修饰的β-NaYF4:Yb,Er NPs,进一步与单克隆抗体偶联后,所得的上转换纳米粒子-抗体缀合物探针用于 LFIA,并作为荧光报告物的信号载体。使用鳗弧菌作为模型分析物来证明该条传感器的用途。荧光条的检测限确定为 10(2) CFU mL(-1),比酶联免疫吸附测定低 100 倍,而检测所需的时间仅为 15 分钟。此外,与其他八种病原体没有交叉反应,表明该条具有良好的特异性。这种开发的 LFIA 将来可能成为定量分析病原体的有用工具。