State Key Laboratory of Food Science and Technology, International Joint Laboratory on Food Safety, Collaborative innovation center of food safety and quality control in Jiangsu Province, Institute of Analytical Food Safety, School of Food Science and Technology, Jiangnan University, Wuxi, 214122, PR China.
Jiangnan University Hospital, Wuxi, 214122, PR China.
Sci Rep. 2020 Jun 15;10(1):9604. doi: 10.1038/s41598-020-66456-1.
Lateral flow assay (LFA) is one of the most prevalent commercially available techniques for point-of-care tests due to its simplicity, celerity, low cost and robust operation. However, conventional colorimetric LFAs have inferior limits of detection (LODs) compared to sophisticated laboratory-based assays. Here, we report a simple strategy of test-zone pre-enrichment to improve the LOD of LFA by loading samples before the conjugate pad assembly. The developed method enables visual LODs of miR-210 mimic and human chorionic gonadotropin protein, to be improved by 10-100 fold compared with a conventional LFA setup without introducing any additional instrument and reagent except for phosphate running buffer, while no obvious difference occurred for Aflatoxin B1 (AFB1). It takes about 6-8 min to enrich every 50 μL of sample diluted with phosphate running buffer, therefore we can get visual results within 20 min. We identified a parameter by modeling the entire process, the concentration of probe-analyte conjugate at test zone when signaling unit being loaded, to be important for the improvement of visual limit of detection. In addition, the test-zone pre-enrichment did not impair the selectivity when miR-210 mimic was adopted as target. Integrated with other optimization, amplification and modification of LFAs, the developed test-zone pre-enrichment method can be applied to further improve LOD of LFAs.
侧向流动分析(LFA)因其简单、快速、低成本和稳健的操作而成为最流行的即时检测商业技术之一。然而,与复杂的基于实验室的检测相比,传统比色 LFAs 的检测限(LOD)较低。在这里,我们报告了一种简单的测试区预富集策略,通过在结合垫组装之前加载样品来提高 LFA 的 LOD。与传统的 LFA 相比,该方法能够将 miR-210 模拟物和人绒毛膜促性腺激素蛋白的视觉 LOD 提高 10-100 倍,而无需引入任何额外的仪器和试剂,除了磷酸盐运行缓冲液,而黄曲霉毒素 B1(AFB1)则没有明显差异。用磷酸盐运行缓冲液稀释每 50 μL 样品需要大约 6-8 分钟进行富集,因此我们可以在 20 分钟内得到可视化结果。我们通过对整个过程进行建模,确定了一个参数,即在加载信号单元时测试区中探针-分析物结合物的浓度对于提高视觉检测限是重要的。此外,当采用 miR-210 模拟物作为靶子时,测试区预富集不会损害选择性。与 LFAs 的其他优化、放大和修饰相结合,开发的测试区预富集方法可用于进一步提高 LFAs 的 LOD。