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基于沉淀的水凝胶颗粒比色多重免疫分析。

Precipitation-based colorimetric multiplex immunoassay in hydrogel particles.

机构信息

Department of Chemical and Biological Engineering, Korea University, Seoul 02841, Republic of Korea.

出版信息

Lab Chip. 2020 Aug 21;20(16):2841-2850. doi: 10.1039/d0lc00325e. Epub 2020 Jul 2.

Abstract

Despite a growing demand for more accessible diagnostic technologies, current methods struggle to simultaneously detect multiple analytes with acceptable sensitivity and portability. Colorimetric assays have been widely used due to their simplicity of signal readout, but the lack of multiplexibility has been a perpetual constraint. Meanwhile, particle-based assays offer multiplex detection by assigning an identity code to each analyte, but they often require lab-based equipment unsuitable for portable diagnostics. Here, by merging the two approaches, this paper reports a colorimetric multiplex immunoassay based on hydrogel microparticles that achieves the best of both worlds. The low-cost portable multiplex assay demonstrates sensitivities as high as and dynamic ranges greater than the lab-based enzyme-linked immunosorbent assay (ELISA). These critical advances are made possible by local precipitation and amplification of insoluble colour dyes inside the hydrogel networks. For the first time, enzymatic accumulation of colour dyes in hydrogel particles is reported and the kinetics of colour development is characterized in this work. By taking advantage of the colour signals in the visible spectrum, the hydrogel microparticles were imaged and analysed using low-cost portable devices. The colorimetric multiplex immunoassay was used to successfully detect three target biomarkers of preeclampsia and validated clinically using healthy and patient-derived plasma samples.

摘要

尽管人们对更易于使用的诊断技术的需求不断增长,但目前的方法在同时以可接受的灵敏度和便携性检测多种分析物方面仍存在困难。比色分析由于其信号读出简单而被广泛应用,但缺乏多重检测能力一直是一个持久的限制。同时,基于粒子的分析方法通过为每个分析物分配唯一的身份代码来实现多重检测,但它们通常需要基于实验室的设备,不适合便携式诊断。在这里,通过合并这两种方法,本文报道了一种基于水凝胶微球的比色多重免疫分析方法,该方法融合了两种方法的最佳优势。这种低成本的便携式多重分析方法具有与基于实验室的酶联免疫吸附测定(ELISA)一样高的灵敏度和更大的动态范围。通过在水凝胶网络内部局部沉淀和放大不溶性显色染料,实现了这些关键的进展。本文首次报道了在水凝胶颗粒中酶促积累显色染料,并对其显色动力学进行了表征。利用可见光谱中的颜色信号,使用低成本的便携式设备对水凝胶微球进行成像和分析。该比色多重免疫分析成功地检测了子痫前期的三个靶标生物标志物,并使用健康和患者来源的血浆样本进行了临床验证。

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