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用于细胞和颗粒高通量分析的微滴微流控技术

Droplet microfluidics for high-throughput analysis of cells and particles.

作者信息

Zagnoni Michele, Cooper Jonathan M

机构信息

Centre for Microsystems and Photonics, Department of Electronic and Electrical Engineering, University of Strathclyde, Glasgow, G1 1XW, UK.

出版信息

Methods Cell Biol. 2011;102:25-48. doi: 10.1016/B978-0-12-374912-3.00002-X.

Abstract

Droplet microfluidics (DM) is an area of research which combines lab-on-a-chip (LOC) techniques with emulsion compartmentalization to perform high-throughput, chemical and biological assays. The key issue of this approach lies in the generation, over tens of milliseconds, of thousands of liquid vessels which can be used either as a carrier, to transport encapsulated particles and cells, or as microreactors, to perform parallel analysis of a vast number of samples. Each compartment comprises a liquid droplet containing the sample, surrounded by an immiscible fluid. This microfluidic technique is capable of generating subnanoliter and highly monodispersed liquid droplets, which offer many opportunities for developing novel single-cell and single-molecule studies, as well as high-throughput methodologies for the detection and sorting of encapsulated species in droplets. The aim of this chapter is to give an overview of the features of DM in a broad microfluidic context, as well as to show the advantages and limitations of the technology in the field of LOC analytical research. Examples are reported and discussed to show how DM can provide novel systems with applications in high-throughput, quantitative cell and particle analysis.

摘要

微滴微流控技术(DM)是一个将芯片实验室(LOC)技术与乳液分隔相结合以进行高通量化学和生物学分析的研究领域。这种方法的关键问题在于在几十毫秒内生成数千个液体容器,这些容器既可以用作载体来运输封装的颗粒和细胞,也可以用作微反应器来对大量样品进行平行分析。每个隔室都包含一个含有样品的液滴,周围是不混溶的流体。这种微流控技术能够生成亚纳升且高度单分散的液滴,这为开展新型单细胞和单分子研究以及用于检测和分选液滴中封装物质的高通量方法提供了许多机会。本章的目的是在广泛的微流控背景下概述DM的特点,并展示该技术在LOC分析研究领域的优势和局限性。报告并讨论了一些实例,以说明DM如何能够提供可应用于高通量定量细胞和颗粒分析的新型系统。

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