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首页> 外文期刊>Analytical chemistry >Ultrashort Separation Length Homogeneous Electrophoretic Immunoassays Using On-Chip Discontinuous Polyacrylamide Gels
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Ultrashort Separation Length Homogeneous Electrophoretic Immunoassays Using On-Chip Discontinuous Polyacrylamide Gels

机译:片上不连续聚丙烯酰胺凝胶的超短分离长度均相电泳免疫分析

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To realize efficient homogeneous electrophoretic immunoassays, we introduce discontinuous polyacrylamide gels that enable quantitative assay completion in separation lengths as short as 350 (mu)m in < 10 s. The discontinuous cross-linked gels reduce the required electrophoretic separation lengths and thereby significantly reduce the required applied electrical potentials needed to achieve 100's V/cm electric field strengths for rapid electrophoresis. To optimize the discontinuous polyacrylamide gel assay format, we demonstrate development of a two-color homogeneous electrophoretic immunoassay for concurrent quantitation of C reactive protein (CRP) and tumor necrosis factor-alpha (TNF-alpha) for monitoring inflammatory response. To achieve necessary pore-size control at the gel discontinuity, an optimized mask-based fabrication protocol is introduced. The fabrication approach improves electrophoretic separations using the discontinuous separation gels by eliminating two confounding phenomena: (1) smaller than desired pores at the discontinuity which result in undesired physical exclusion of large-species and (2) an associated transition from small to large pores aft of the interface which acts to "destack" analyte bands during the separation. With the use of the optimized discontinuous separation gels, both assays were linear and quantitative over a two-log detection range, with a lower limit of detection of 11 ng/mL for CRP and 40 ng/mL for TNF-alpha. An optimal single-point detector location was identified by balancing the separation resolution and assay duration constraints. The ultrashort separation distance electrophoretic assays developed here provide flexibility in chip and instrument design by relaxing electrical potential requirements and expanding the possibilities for assay multiplexing, therefore addressing important design considerations when developing field-portable diagnostic assays for near-patient environments.
机译:为了实现有效的均相电泳免疫测定,我们引入了不连续的聚丙烯酰胺凝胶,该凝胶能够在短于10 s的短至350μm的分离长度内完成定量测定。不连续的交联凝胶减少了所需的电泳分离长度,从而显着减少了实现快速电泳所需的100伏特/厘米电场强度所需的施加电势。为了优化不连续聚丙烯酰胺凝胶测定法的形式,我们证明了用于同时定量C反应蛋白(CRP)和肿瘤坏死因子-α(TNF-alpha)监测炎症反应的双色均相电泳免疫测定法的发展。为了在凝胶间断处实现必要的孔径控制,引入了优化的基于掩模的制造方案。该制造方法通过消除两个混淆现象来改善使用不连续分离凝胶的电泳分离:(1)在不连续处小于所需的孔,这导致大分子的不期望的物理排斥;(2)从后向小孔到大孔的相关过渡界面的作用是在分离过程中“分解”分析物谱带。通过使用优化的不连续分离凝胶,两种测定在两个对数检测范围内都是线性和定量的,对于CRP和TNF-alpha的检测下限均为11 ng / mL。通过平衡分离分辨率和化验时间限制,确定了最佳的单点检测器位置。此处开发的超短分离距离电泳测定法通过放宽电势要求并扩展测定法多重化的可能性,为芯片和仪器设计提供了灵活性,因此在开发适用于近患者环境的现场便携式诊断测定法时解决了重要的设计注意事项。

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