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采用微流控 ELISA 技术和磁珠定量检测血清总 IgE。

Total serum IgE quantification by microfluidic ELISA using magnetic beads.

机构信息

Laboratoire d'Electrochimie Physique et Analytique, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LEPA, Station 6, 1015 Lausanne, Switzerland.

出版信息

Anal Bioanal Chem. 2012 Mar;402(8):2645-53. doi: 10.1007/s00216-011-5495-0. Epub 2011 Oct 22.

DOI:10.1007/s00216-011-5495-0
PMID:22021022
Abstract

The present work reports on the quantification of total IgE in human serum using a microanalytical device whose fluidics is driven by gravity and capillary forces only. Thanks to the eight parallel microchannels in each microchip, calibration and sample analysis are performed simultaneously. A mixture of magnetic bead/analyte/second antibody is incubated off-line and then percolated through the channels where magnetic beads are trapped, enabling the separation of the solid phase from the excess reagents. The entire assay is performed in less than 1 h, and thanks to the miniaturized format, only a small volume of serum is required. Non-specific adsorption was first investigated and a blocking agent compatible with this allergy-based test was chosen. Then, the assay was optimized by determining the best magnetic bead and labelled antibody concentrations. After achievement of a calibration curve with a reference material, the protocol was applied to total IgE quantification of a patient serum sample that showed results in good accordance with those obtained by ImmunoCap® and Immunoaffinity capillary electrophoresis measurements. A detection limit of 17.5 ng ml(-1) was achieved and good reproducibility (RSD < 10%) inter- and intra-chip was observed.

摘要

本工作报告了一种仅使用重力和毛细作用力驱动流体的微分析装置来定量检测人血清中的总 IgE。由于每个微芯片中有 8 条平行的微通道,因此可以同时进行校准和样品分析。将磁珠/分析物/第二抗体的混合物离线孵育,然后通过通道渗透,在通道中捕获磁珠,从而实现固相与多余试剂的分离。整个测定在不到 1 小时内完成,由于采用了微缩格式,仅需少量血清。首先研究了非特异性吸附,并选择了与这种基于过敏的测试兼容的封闭剂。然后,通过确定最佳的磁珠和标记抗体浓度对测定进行了优化。在使用参考物质获得校准曲线后,该方案被应用于患者血清样品中总 IgE 的定量检测,其结果与 ImmunoCap®和免疫亲和毛细管电泳测量的结果非常一致。检测限达到 17.5ngml(-1),并且在芯片间和芯片内观察到良好的重现性(RSD<10%)。

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