Université Paris-Saclay, CNRS, Institut Galien Paris-Saclay, 91400, Orsay, France.
Université Paris-Saclay, CNRS, Institut Galien Paris-Saclay, 91400, Orsay, France.
Anal Chim Acta. 2023 May 15;1255:341141. doi: 10.1016/j.aca.2023.341141. Epub 2023 Mar 24.
This study reports on the development of a new concept of on-line dual preconcentration stages for capillary electrophoresis (CE), in which two completely different preconcentration approaches can be realized in the same capillary. In the first stage, a dynamic magneto-extraction of target analytes on circulating magnetic beads is implemented within the capillary. In the second one, electrokinetic preconcentration of eluted analytes via large volume sample stacking is carried out to focus them into a nano band, prior to CE separation of enriched analytes. To implement the dual-stage preconcentration operation, a purpose-made instrument was designed, combining electrophoretic and microfluidic modules to allow precise control of the movement of magnetic beads and analyte's flow. The potential of this new enrichment principle and its associated instrument was demonstrated for CE separation with light-emitting-diode-induced fluorescent (LEDIF) detection of target double-stranded DNA (ds-DNA). The workflow consists of purification and preconcentration of a target DNA fragment (300 bp) on negatively charged magnetic beads, followed by in-capillary elution and fluorescent labelling of the enriched DNA. Large volume sample stacking of the DNA eluent was then triggered to further preconcentrate the labelled DNA before its analysis by CE-LEDIF. An enrichment factor of 125 was achieved for the target DNA fragment. With our new approach, dual-stage sample pretreatment and CE separation can now be performed in-capillary without any mismatch of working volumes, nor any waste of pretreated samples.
本研究报告了一种毛细管电泳(CE)在线双预浓缩阶段的新概念,其中两种完全不同的预浓缩方法可在同一毛细管中实现。在第一阶段,通过在毛细管内循环磁性珠上的动态磁萃取来实现目标分析物的萃取。在第二阶段,通过大体积样品堆积进行洗脱分析物的电动浓缩,将其聚焦成纳米带,然后进行CE 分离富集的分析物。为了实现双阶段预浓缩操作,设计了一种专用仪器,将电泳和微流控模块结合在一起,以精确控制磁性珠和分析物的流动。该新的富集原理及其相关仪器的潜力已通过发光二极管诱导荧光(LEDIF)检测目标双链 DNA(ds-DNA)的 CE 分离得到证明。工作流程包括在带负电荷的磁性珠上对目标 DNA 片段(300 bp)进行纯化和预浓缩,然后在毛细管内洗脱并对富集的 DNA 进行荧光标记。然后触发 DNA 洗脱液的大体积样品堆积,以在通过 CE-LEDIF 分析之前进一步浓缩标记的 DNA。目标 DNA 片段的富集因子达到 125。通过我们的新方法,现在可以在毛细管内进行双阶段样品预处理和 CE 分离,而不会出现工作体积不匹配或预处理样品浪费的情况。