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通过微流控液滴发生器对HPLC底物进行毛细管分级分离以实现高通量分析。

Capillary fractionation of HPLC substrates by a microfluidic droplet generator for high throughput analysis.

作者信息

Hamed Shereef, Shay Brian, Basu Amar S

机构信息

Department of Biomedical Engineering, Wayne State University, Detroit, MI, USA.

出版信息

Annu Int Conf IEEE Eng Med Biol Soc. 2011;2011:8396-9. doi: 10.1109/IEMBS.2011.6092071.

Abstract

Biochemical samples are complex mixtures containing 1000's of components which often must be fractionated prior to analysis. Conventional fraction collectors, which can only accommodate 10's of fractions, are not well suited for high throughput analysis. This paper describes microfractionation in droplets (μFD), a scalable microfluidic technique for generating thousands of fractions. A drop generator, placed downstream from a high performance liquid chromatography (HPLC) column, encapsulates the separated components into a serial array of monodisperse droplets. The droplets can be stored in a capillary or immediately used in subsequent assays. Using μFD, a mixture of 3 dyes separated in a C18 column was fractionated into 2,160 droplets in <6 min. The volume and frequency of the droplet fractions are governed by the capillary number (Ca), which depends on the viscosity of the carrier fluid, flow rate, and interfacial tension. With HPLC-compatible flow rates of 0.38-0.7 mL/min, in a 1.5 mm Teflon capillary, fractions contain volumes of 1-6 μL and are generated at 2-10 drops/s. Droplet fractions can be mixed with a subsequent reagent using a downstream tee junction. In theory, μFD can be coupled to a wide variety of separation processes, enabling high throughput fractionation and screening of complex mixtures in μL to sub-nL volumes.

摘要

生化样品是包含数千种成分的复杂混合物,在分析之前通常必须进行分离。传统的馏分收集器只能容纳十几个馏分,不太适合高通量分析。本文介绍了液滴微分离(μFD),这是一种可扩展的微流控技术,用于生成数千个馏分。一个位于高效液相色谱(HPLC)柱下游的液滴发生器,将分离出的成分封装到一系列单分散液滴中。这些液滴可以储存在毛细管中或立即用于后续分析。使用μFD,在C18柱中分离的三种染料混合物在不到6分钟内被分离成2160个液滴。液滴馏分的体积和频率由毛细管数(Ca)决定,毛细管数取决于载液的粘度、流速和界面张力。在1.5毫米的聚四氟乙烯毛细管中,以与HPLC兼容的0.38 - 0.7毫升/分钟的流速,馏分的体积为1 - 6微升,生成速度为每秒2 - 10滴。液滴馏分可以使用下游三通接头与后续试剂混合。理论上,μFD可以与多种分离过程相结合,实现对微升至亚纳升体积的复杂混合物进行高通量分离和筛选。

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