Simple surface modification of poly(methyl methacrylate) microfluidic microplates for enhanced ultrasensitive multiplexed detection of infectious diseases

Sharma T. Sanjay , Sapna Kannan , XiuJun Li
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Abstract

Novel strategies for the simultaneous and portable detection of multiple analytes are highly favorable for clinical diagnosis and healthcare. Conventional colorimetric enzyme-linked immunosorbent assay (ELISA) is a widely used laboratory technique for medical diagnostics, quality control, and research applications. However, nonspecific absorption of proteins may lead to a reduction of functional sites, resulting in high background and low sensitivity in ELISA. Herein, we report a simple method of functionalization of poly(methyl methacrylate) (PMMA) with polylysine to be used as the microfluidic microplate substrate for enhanced ELISA, enabling rapid, ultrasensitive, and multiplexed detection of infectious diseases. FTIR and fluorescence microscopy characterization confirmed high amine densities on polylysine-modified PMMA surface, resulting in high detection sensitivity of the colorimetric ELISA on the PMMA microdevice. The ultrasensitive polylysine-modified microplate can immobilize protein within 20 min and results of the assay can be viewed by the naked eye or scanned through a simple desktop scanner for quantitative analysis within 90 min. A sandwich-type immunoassay for the rapid and sensitive detection of immunoglobulin G (IgG), hepatitis B surface antigen (HBsAg), and hepatitis B core antigen (HBcAg) was demonstrated as a proof-of-concept for multiplexed detection. The limits of detection (LOD) of 200.0 pg/mL for IgG, 180.0 pg/mL for HBsAg, and 300.0 pg/mL for HBcAg were achieved, without any specialized equipment like a microplate reader. The surface-modified microchip exhibited about 10-fold higher sensitivity than traditional microplates. This surface-modified microplate has tremendous potential as a point-of-care multiplexed testing platform for many applications ranging from clinical diagnosis to environmental monitoring, particularly in resource-limited settings.
聚甲基丙烯酸甲酯微流控微孔板的简单表面修饰,增强了传染病的超灵敏多路检测
同时便携式检测多种分析物的新策略对临床诊断和医疗保健非常有利。传统的比色酶联免疫吸附测定(ELISA)是一种广泛应用于医学诊断、质量控制和研究的实验室技术。然而,蛋白质的非特异性吸收可能导致功能位点的减少,导致ELISA的高背景和低灵敏度。在此,我们报告了一种用聚赖氨酸功能化聚甲基丙烯酸甲酯(PMMA)的简单方法,作为微流控微孔板底物,用于增强ELISA,实现快速、超灵敏和多路检测传染病。FTIR和荧光显微镜表征证实,聚赖氨酸修饰的PMMA表面具有较高的胺密度,使得比色ELISA在PMMA微装置上具有较高的检测灵敏度。超灵敏的聚赖氨酸修饰的微孔板可在20分钟内固定蛋白,检测结果可在90分钟内肉眼观察或通过简单的台式扫描仪扫描进行定量分析。用于快速灵敏检测免疫球蛋白G (IgG),乙型肝炎表面抗原(HBsAg)和乙型肝炎核心抗原(HBcAg)的三明治型免疫分析法被证明是一种多路检测的概念验证。IgG的检出限(LOD)为200.0 pg/mL, HBsAg为180.0 pg/mL, HBcAg为300.0 pg/mL,无需任何专用设备,如微孔板阅读器。表面修饰的微芯片显示出比传统微孔板高10倍的灵敏度。这种表面修饰的微孔板具有巨大的潜力,可作为从临床诊断到环境监测等许多应用的即时多路测试平台,特别是在资源有限的环境中。
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