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通过电渗流辅助的胶束增溶至溶剂微萃取实现电泳中的堆积。

Stacking in electrophoresis by electroosmotic flow-assisted admicelle to solvent microextraction.

作者信息

Vaas Andaravaas Patabadige Jude P, Yu Raymond B, Quirino Joselito P

机构信息

Australian Centre for Research On Separation Science (ACROSS), School of Natural Sciences-Chemistry, University of Tasmania, Private Bag 75, Hobart, TAS, 7001, Australia.

Department of Pharmaceutical Chemistry, College of Pharmacy, University of the Philippines Manila, Manila, Philippines.

出版信息

Anal Bioanal Chem. 2024 Dec;416(29):6789-6798. doi: 10.1007/s00216-024-05554-9. Epub 2024 Oct 2.

Abstract

An in-line sample concentration method for capillary electrophoresis called admicelle to solvent microextraction was proposed. In this technique, analytes were trapped in the cetyltrimethylammonium bromide admicelles formed in situ on the negatively charged capillary surface. A solvent plug was then partially injected hydrodynamically to collapse the admicelles, which liberated and focused the analytes at the solvent front. Voltage was applied across the capillary, completing the stacking process. Various solvents, namely, methanol, ethanol, and acetonitrile, were investigated. The optimal solvent for solvent to admicelle microextraction was 30% acetonitrile in 24 mM sodium tetraborate (pH 9.2). Sample injection time and solvent to sample injection ratio were also optimised. For this demonstration, the optimum sample injection time and solvent to sample injection ratio were 320 s and 1:2, respectively. Using the optimum conditions, UV detection sensitivity was enhanced 132-176-fold for the model anions. The LOQ, %intra-/inter-day (n = 6/n = 12, 2 days) repeatability, and linearity (R) of admicelle to solvent microextraction were 0.08-2 µg/mL, 1.9-3.9%, 2.8-4.9%, and 0.992, respectively. Admicelle to solvent microextraction was applied to the analysis of various fortified water samples, with good repeatability (%RSD = 0.5-3.6%), and no matrix interferences.

摘要

提出了一种用于毛细管电泳的在线样品浓缩方法,称为辅助胶束到溶剂微萃取。在该技术中,分析物被困在带负电荷的毛细管表面原位形成的十六烷基三甲基溴化铵辅助胶束中。然后通过流体动力学部分注入溶剂塞以使辅助胶束塌陷,从而使分析物在溶剂前沿释放并聚焦。在毛细管两端施加电压,完成堆积过程。研究了各种溶剂,即甲醇、乙醇和乙腈。用于溶剂到辅助胶束微萃取的最佳溶剂是在24 mM硼酸钠(pH 9.2)中的30%乙腈。还优化了进样时间和溶剂与样品进样比。对于本演示,最佳进样时间和溶剂与样品进样比分别为320 s和1:2。在最佳条件下,模型阴离子的紫外检测灵敏度提高了132-176倍。辅助胶束到溶剂微萃取的定量限、日内/日间重复性(n = 6/n = 12,2天)和线性度(R)分别为0.08-2 μg/mL、1.9-3.9%、2.8-4.9%和0.992。辅助胶束到溶剂微萃取应用于各种加标水样的分析,具有良好的重复性(%RSD = 0.5-3.6%),且无基质干扰。

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