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在毛细管内形成聚合物/表面活性剂配合物辅助反向迁移胶束电动色谱法,用于方便地分析中性甾体。

In-capillary formation of polymer/surfactant complexes-assisted reversed-migration micellar electrokinetic chromatography for facile analysis of neutral steroids.

机构信息

Department of Applied Chemistry, Laboratory of Biomedical and Analytical Technologies, National Chi Nan University, Puli, Nantou 54561, Taiwan.

出版信息

Talanta. 2013 Mar 30;107:389-95. doi: 10.1016/j.talanta.2013.01.036. Epub 2013 Feb 4.

Abstract

In this study we developed a novel approach, using in-capillary formation of polymer/surfactant complexes (IPSC)-assisted reversed-migration MEKC (RM-MEKC), for the analysis of neutral steroids. This process involved two sequential events: in-capillary polymer/surfactant complexes formation during sample preconcentration, followed by IPSC separation. The procedure began with a polymer-filled capillary. Initially, on-line preconcentration of the sample was performed at the sample plug. Meanwhile, free surfactants migrated to interact with polymers, forming polymer-surfactant complexes. Analytes were then kinetically partitioned between the mixed phases (micelles and polymer-SDS complexes). Sodium dodecyl sulfate (SDS) and poly(N-isopropylacrylamide) (PNIPAAm) were employed as pseudo-stationary phases (PSPs). This system allowed the successful separation of five steroids (testosterone, hydrocortisone 21-acetate, dexamethasone, prednisolone, hydrocortisone) in acetate buffer and the determination of urinary free hydrocortisone; it also exhibited excellent performance for sample on-line concentration. The limit of detection for hydrocortisone was 20.98 ng/mL (R(2)=0.9995). The polymer size, concentrations, end-group charges, and SDS concentrations were evaluated. This IPSC/RM-MEKC system, which can be adopted in commercial CE instruments, is easy to operate, suitable for combination with several sample preconcentration options, sensitive, robust, and environmentally sustainable. We suspect that such systems might have potential applications in clinical analyses and in microanalytical devices.

摘要

在本研究中,我们开发了一种新方法,即使用在毛细管内形成的聚合物/表面活性剂复合物(IPSC)辅助反迁移 MEKC(RM-MEKC),用于分析中性甾体。该过程涉及两个连续事件:在样品预浓缩过程中在毛细管内形成聚合物/表面活性剂复合物,随后进行 IPSC 分离。该过程从充满聚合物的毛细管开始。最初,在样品塞上进行在线样品预浓缩。同时,游离表面活性剂迁移以与聚合物相互作用,形成聚合物-表面活性剂复合物。然后,分析物在混合相(胶束和聚合物-SDS 复合物)之间进行动力学分配。十二烷基硫酸钠(SDS)和聚(N-异丙基丙烯酰胺)(PNIPAAm)被用作伪固定相(PSPs)。该系统允许在乙酸盐缓冲液中成功分离五种甾体(睾酮、21-乙酸氢化可的松、地塞米松、泼尼松龙、氢化可的松)并测定尿游离氢化可的松;它还表现出出色的在线浓缩样品性能。氢化可的松的检测限为 20.98ng/mL(R²=0.9995)。评估了聚合物的大小、浓度、端基电荷和 SDS 浓度。这种 IPSC/RM-MEKC 系统可用于商业 CE 仪器,操作简单,适合与几种样品预浓缩选项结合使用,具有灵敏度高、稳健性强和环境可持续性等特点。我们怀疑这种系统可能在临床分析和微分析设备中有潜在的应用。

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