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通过电动溶剂配比实现微流控免疫分析的集成自校准

Integrated self-calibration via electrokinetic solvent proportioning for microfluidic immunoassays.

作者信息

Qiu C X, Harrison D J

机构信息

Department of Chemistry, University of Alberta, Edmonton, Canada.

出版信息

Electrophoresis. 2001 Oct;22(18):3949-58. doi: 10.1002/1522-2683(200110)22:18<3949::AID-ELPS3949>3.0.CO;2-7.

Abstract

On-board generation of a set of calibration standards was demonstrated within a microfluidic device designed to perform immunoassay. Electrokinetic flow was used to proportionally mix the antibody (Ab) to bovine serum albumin (BSA) and a diluting buffer, to provide varying Ab concentrations for downstream mixing with fluorescently labeled BSA (BSA*). Mixing ratios were determined from electrical impedance modeling of the fluidic network using P-SPICE software, and peak heights for the labeled species were analyzed relative to the concentration calculated from the model. For dilution and separation of fluorescently labeled amino acids, a linear calibration curve was obtained for mixing ratios of 0.118 to 7.46. A linear calibration curve was obtained for the immunoassay calibration using dilution ratios between 0.197 and 5.077. Deviations were observed at larger extremes, possibly due to leakage effects at intersections. Peak height reproducibility was +/- 3% for the immunoassay, using diluted monoclonal Ab in mouse ascites fluid as the analyte. Recovery for on-chip calibration was 92 +/- 6% versus calibrants prepared off-chip, indicating a small bias.

摘要

在一个设计用于进行免疫测定的微流控装置中展示了一组校准标准品的片上生成。利用电动流按比例将抗体(Ab)与牛血清白蛋白(BSA)和稀释缓冲液混合,以提供不同的Ab浓度用于下游与荧光标记的BSA(BSA*)混合。使用P-SPICE软件通过流体网络的电阻抗建模确定混合比例,并相对于根据模型计算的浓度分析标记物种的峰高。对于荧光标记氨基酸的稀释和分离,在0.118至7.46的混合比例下获得了线性校准曲线。使用0.197至5.077的稀释比例进行免疫测定校准获得了线性校准曲线。在更大的极端情况下观察到偏差,可能是由于交叉点处的泄漏效应。使用小鼠腹水中稀释的单克隆Ab作为分析物,免疫测定的峰高重现性为+/- 3%。与片外制备的校准物相比,片上校准的回收率为92 +/- 6%,表明存在小偏差。

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