Microdroplets: A sea of applications?

被引:524
作者
Huebner, Ansgar [2 ,3 ]
Sharma, Sanjiv [4 ]
Srisa-Art, Monpichar [1 ]
Hollfelder, Florian [3 ]
Edel, Joshua B. [1 ,4 ]
deMello, Andrew J. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
[2] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[3] Univ Cambridge, Dept Biochem, Cambridge CB2 1GA, England
[4] Univ London Imperial Coll Sci Technol & Med, Inst Biomed Engn, London SW7 2AZ, England
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1039/b806405a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The exploitation of microdroplets produced within microfluiclic environments has recently emerged as a new and exciting technological platform for applications within the chemical and biological sciences. Interest in microfluidic systems has been stimulated by a range of fundamental features that accompany system miniaturization. Such features include the ability to process and handle small volumes of fluid, improved analytical performance when compared to macroscale analogues, reduced instrumental footprints, low unit cost, facile integration of functional components and the exploitation of atypical fluid dynamics to control molecules in both time and space. Moreover, microfluidic systems that generate and utilize a stream of sub-nanolitre droplets dispersed within an immiscible continuous phase have the added advantage of allowing ultra-high throughput experimentation and being able to mimic conditions similar to that of a single cell (in terms of volume, pH, and salt concentration) thereby compartmentalizing biological and chemical reactions. This review provides an overview of methods for generating, controlling and manipulating droplets. Furthermore, we discuss key fields of use in which such systems may make a significant impact, with particular emphasis on novel applications in the biological and physical sciences.
引用
收藏
页码:1244 / 1254
页数:11
相关论文
共 142 条
[11]   In vitro compartmentalization by double emulsions: sorting and gene enrichment by fluorescence activated cell sorting [J].
Bernath, K ;
Hai, MT ;
Mastrobattista, E ;
Griffiths, AD ;
Magdassi, S ;
Tawfik, DS .
ANALYTICAL BIOCHEMISTRY, 2004, 325 (01) :151-157
[12]  
BERTHIER J, 2006, MICROFLUIDS BIOTECHN
[13]   Emulsions: basic principles [J].
Bibette, J ;
Calderon, FL ;
Poulin, P .
REPORTS ON PROGRESS IN PHYSICS, 1999, 62 (06) :969-1033
[14]   Microfluidics: in search of a killer application [J].
Blow, Nathan .
NATURE METHODS, 2007, 4 (08) :665-668
[15]   Decompressing emulsion droplets favors coalescence [J].
Bremond, Nicolas ;
Thiam, Abdou R. ;
Bibette, Jerome .
PHYSICAL REVIEW LETTERS, 2008, 100 (02)
[16]   Microfluidics-based systems biology [J].
Breslauer, DN ;
Lee, PJ ;
Lee, LP .
MOLECULAR BIOSYSTEMS, 2006, 2 (02) :97-112
[17]   Microfluidic systems for chemical kinetics that rely on chaotic mixing in droplets [J].
Bringer, MR ;
Gerdts, CJ ;
Song, H ;
Tice, JD ;
Ismagilov, RF .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 2004, 362 (1818) :1087-1104
[18]  
BROUZES E, 2006, P MU TAS, P1043
[19]   Writing with DNA and protein using a nanopipet for controlled delivery [J].
Bruckbauer, A ;
Ying, LM ;
Rothery, AM ;
Zhou, DJ ;
Shevchuk, AI ;
Abell, C ;
Korchev, YE ;
Klenerman, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (30) :8810-8811
[20]   Droplet fusion by alternating current (AC) field electrocoalescence in microchannels [J].
Chabert, M ;
Dorfman, KD ;
Viovy, JL .
ELECTROPHORESIS, 2005, 26 (19) :3706-3715