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高通量纳升级液体-液体萃取。

High-Throughput Liquid-Liquid Extractions with Nanoliter Volumes.

机构信息

Department of Chemistry , University of Michigan , 930 North University Avenue , Ann Arbor , Michigan 48109-1055 , United States.

出版信息

Anal Chem. 2020 Feb 18;92(4):3189-3197. doi: 10.1021/acs.analchem.9b04915. Epub 2020 Feb 6.

DOI:10.1021/acs.analchem.9b04915
PMID:31986881
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7814290/
Abstract

Current methods for liquid-liquid extractions generally require microliter to milliliter volumes of solvents and sample, long equilibration times, and manual procedures. Extraction methods for samples in microfluidic systems have been limited as this tool is difficult to implement on the nanoliter or smaller scale. We have developed slug-flow nanoextraction (SFNE), a method based on droplet microfluidics that allows multiple liquid-liquid extractions to be performed simultaneously in a capillary tube, using only 5 nL of sample and extraction solvent per extraction. Each two-phase slug is segmented from the others by immiscible carrier fluid. We found rapid extractions (<5 s), partition coefficients matching those achieved at larger scale extractions, and potential to preconcentrate samples through volume manipulation. This method was used to accurately and rapidly determine octanol-water partition coefficients (), determining identical as the shake-flask method for acetaminophen, = 2.48 ± 0.02. The measurement, along with calibration and 12 replicates, was complete within 5 min, consuming under 150 nL of solvent and sample. The method was also applied to extract analytes from complex biological samples prior to electrospray ionization-tandem mass spectrometry (ESI-MS/MS) at a rate of 6 s per sample, allowing for simultaneous determination of five different drugs spiked into human plasma, synthetic urine (SU), and artificial cerebral spinal fluid (aCSF) using ethyl acetate as the extraction phase. The signal-to-noise (S/N) for analytes improved up to 19-fold compared to direct ESI-MS of single-phase droplets (aqueous plugs segmented by carrier fluid), with limits of detection down to 7 nM (35 amol).

摘要

目前的液-液萃取方法通常需要微升至毫升级的溶剂和样品体积、长时间的平衡时间和手动操作。微流控系统中的样品萃取方法受到限制,因为这种工具难以在纳升到更小的规模上实施。我们开发了液滴微流控技术为基础的段塞流纳米萃取 (SFNE),该方法可以在毛细管中同时进行多次液-液萃取,每次萃取仅使用 5 nL 的样品和萃取溶剂。每个两相段塞通过不混溶的载流液与其他段塞分离。我们发现快速萃取(<5 s)、与较大规模萃取相当的分配系数,以及通过体积操作浓缩样品的潜力。该方法用于准确快速地测定辛醇-水分配系数 (), 确定对乙酰氨基酚的 与摇瓶法相同,= 2.48 ± 0.02。该测量值、校准值和 12 个重复值在 5 分钟内完成,消耗的溶剂和样品少于 150 nL。该方法还用于在电喷雾串联质谱 (ESI-MS/MS) 之前从复杂的生物样品中提取分析物,每个样品的速度为 6 s,允许同时测定五种不同的药物掺入人血浆、合成尿 (SU) 和人工脑脊液 (aCSF),使用乙酸乙酯作为萃取相。与单相液滴(由载流液分段的水相塞)的直接 ESI-MS 相比,分析物的信噪比 (S/N) 提高了 19 倍,检测限低至 7 nM(35 amol)。