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2-D t-ITP/CZE determination of clinical urinary proteins using a microfluidic-chip capillary electrophoresis device†

机译:使用微流控芯片毛细管电泳设备二维二维ITP / CZE测定临床尿蛋白†

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摘要

To replace the time-consuming sample pretreatment procedure, a microfluidic chip-CE device incorporating on-chip sample desalting/preconcentration with transient isotachophoresis (ITP)/capillary zone electrophoresis (CZE) was fabricated to perform sequential on-chip sample pretreatment and CE determination of four urinary proteins in clinical samples. On-chip sample desalting, clean-up and analyte preconcentration enable removing interfering sample matrix prior to transferring analytes to separation capillary for transient ITP/CZE determination. Four important urinary proteins transferrin, β2-microglobulin, human serum albumin (HSA) and immunoglobulin G (IgG), investigated were shown to achieve quantitation limits sufficiently high to meet medical requirements, sensitivity enhancement up to 40-fold and detection limits down to 0.3, 0.05, 0.6, 0.5 mg/L, respectively. Compared to the stacking effect, the use of a large sample size was found to be the major factor for sensitivity enhancement. The method reliability is established by close to 100% recoveries and statistical agreement of results from the method developed with currently used clinical radio-immunoassay method for all four proteins investigated. Moreover, an assay time of less than 10 min is needed in the method developed as compared to 7 h for the radio-immunoassay method.
机译:为了取代耗时的样品预处理程序,制造了一种微流控芯片CE设备,该设备将芯片上样品脱盐/预浓缩与瞬时等速电泳(ITP)/毛细管区带电泳(CZE)结合在一起,以进行顺序的芯片上样品预处理和CE测定临床样本中的四种尿蛋白含量片上样品脱盐,净化和分析物预浓缩能够在将分析物转移到分离毛细管上进行瞬时ITP / CZE测定之前去除干扰的样品基质。研究表明,对四种重要的尿蛋白转铁蛋白,β2-微球蛋白,人血清白蛋白(HSA)和免疫球蛋白G(IgG)进行了定量分析,足以满足医学要求,灵敏度提高了40倍,检出限降低到0.3分别为0.05、0.6、0.5μmg / L。与堆积效应相比,发现使用大样本量是提高灵敏度的主要因素。该方法的可靠性是通过将近100%的回收率建立的,并且该方法的结果与目前使用的临床放射免疫测定方法开发的所有四种蛋白质的开发结果之间的统计一致性也得以确立。而且,与放射免疫测定法的7 h相比,开发的方法所需的测定时间少于10分钟。

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