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基于 PDMS 的数字磁流体的 C 反应蛋白快速简便免疫测定法。

A rapid and facile immunoassay for C-reactive protein using PDMS-based digital magnetofluidics.

机构信息

Electrochemistry and Optical Spectroscopy Center of Excellence, Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand.

A Sensor Research Unit (SRU), Department of Chemistry, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand; Research Network NANOTEC-CU on Advanced Structural and Functional Nanomaterials, Faculty of Science, Chulalongkorn University, Pathumwan, Bangkok, 10330, Thailand.

出版信息

Anal Chim Acta. 2024 Sep 8;1321:343044. doi: 10.1016/j.aca.2024.343044. Epub 2024 Aug 2.

Abstract

BACKGROUND

C-reactive protein has been reported as a biomarker of inflammation caused by acute injury, infection or tissue damage and also a prediction marker of cardiovascular diseases. Commonly, the gold standard for the detection of CRP is enzyme-linked immunosorbent assays (ELISAs). Normally, traditional immunoassays in multiwell plates typically suffer from prolonged assay time due to slow mass transport controlled by diffusion. Herein, a PDMS based magnetofluidic approach has been applied for a rapid and facile immunoassay using a sandwich enzyme-linked immunosorbent assay (ELISA) for the analysis of CRP.

RESULTS

Due to the superhydrophobic PDMS, droplets of reagent and sample solutions were obtained when pipetting all solutions onto the PDMS substrate. These droplets were individually controlled by an external magnet to perform the assays. Magnetic beads immobilized with a capture antibody were not only used for immunomagnetic separation (IMS) of the captured CRP from the sample matrix, but also used as a carrier for droplet movement on the magnetofluidic device, expediting the immunoassay procedure, especially washing steps. The immunoassay of CRP was successfully performed within 1 h with a limit of detection of 0.015 mg L in the concentration range of 0.1-10 mg L. The recovery percentages of CRP spiked in human serum were found in the range of 90-114 % with %RSD of less than 5 %, indicating acceptable accuracy and precision.

SIGNIFICANCE

By individually controlling the droplet movement using an external magnet, all steps of immunoassays were simply and rapidly performed. In addition, the microfluidic format allows for small volumes of reagents and samples and rapid assay kinetics. Therefore, the proposed magnetofluidic approach has shown its potential of becoming a rapid, facile and cost-effective method to perform traditional immunoassays in a variety of applications. In addition, the proposed approach is also particularly well-suited for analyses/reactions with multiple steps.

摘要

背景

C-反应蛋白已被报道为急性损伤、感染或组织损伤引起的炎症的生物标志物,也是心血管疾病的预测标志物。通常,检测 CRP 的金标准是酶联免疫吸附测定(ELISA)。通常,由于扩散控制的质量传输缓慢,多孔板中的传统免疫测定通常需要较长的测定时间。在此,已经应用基于 PDMS 的磁流体方法用于使用夹心酶联免疫吸附测定(ELISA)进行快速简便的 CRP 分析的免疫测定。

结果

由于 PDMS 的超疏水性,当将所有溶液吸取到 PDMS 基底上时,会得到试剂和样品溶液的液滴。这些液滴通过外部磁铁单独控制以进行测定。固定有捕获抗体的磁性珠不仅用于从样品基质中免疫磁分离(IMS)捕获的 CRP,而且还用作在磁流体装置上移动液滴的载体,从而加速免疫测定过程,特别是洗涤步骤。CRP 的免疫测定在 1 小时内成功完成,在 0.1-10mg/L 的浓度范围内检测限为 0.015mg/L。在人血清中添加 CRP 的回收率在 90-114%范围内,相对标准偏差(%RSD)小于 5%,表明具有可接受的准确性和精密度。

意义

通过使用外部磁铁单独控制液滴的运动,可以简单快速地进行免疫测定的所有步骤。此外,微流控格式允许使用小体积的试剂和样品,并具有快速的测定动力学。因此,所提出的磁流体方法已显示出在各种应用中成为快速、简便且具有成本效益的传统免疫测定方法的潜力。此外,该方法还特别适合具有多个步骤的分析/反应。

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