期刊文献+

液滴微流控芯片系统中微液滴特性表征及氨基酸检测应用 被引量:5

Micro-dropleMicro-droplet characterization and its application for amino acid detection in droplet microfluidic system
原文传递
导出
摘要 基于液滴微流控芯片的检测和筛选系统,因其具有通量高、成本低等显著特点,近年来备受关注。该系统生成的微液滴(皮升体积)具有直径均一、大小可控、互不交融(单分散性)等特性,它作为微反应器可以进行微生物及其代谢物包埋实验和高通量检测。因此,研究微液滴的相关特性及其应用具有重要意义。文中在液滴微流控芯片系统搭建的基础上,对重要氨基酸(谷氨酸、苯丙氨酸、色氨酸和酪氨酸)分别进行了微液滴包埋实验,研究了包埋微液滴的重要特性参数(如稳定性、扩散性等),探索了包埋微液滴对氨基酸检测分选的应用。实验表明,文中搭建的液滴微流控芯片系统可以稳定、均一地生成微液滴,微液滴大小可根据需要控制在2 0-5 0μm之间,微液滴间无交叉污染,包埋氨基酸的微液滴的检测筛选速度大约为每分钟6 0 0个。这个研究为高通量分析和筛选产氨基酸的微生物奠定了基础。 Recently, the droplet microfluidic system attracts interests due to its high throughput and low cost to detect and screen. The picoliter micro-droplets from droplet microfluidics are uniform with respect to the size and shape, and could be used as monodispensed micro-reactors for encapsulation and detection of single cell or its metabolites. Therefore, it is indispensable to characterize micro-droplet and its application from droplet microfluidic system. We first constructed the custom-designed droplet microfluidic system for generating micro-droplets, and then used the micro-droplets to encapsulate important amino acids such as glutamic acid, phenylalanine, tryptophan or tyrosine to test the droplets' properties, including the stability, diffusivity and bio-eompatibility for investigating its application for amino acid detection and sorting. The custom-designed droplet microfluidic system could generate the uniformed micro-droplets with a controllable size between 20 to 50 ~tm. The micro-droplets could be stable for more than 20 h without cross-contamination or fusion each other. The throughput of detection and sorting of the system is about 600 micro-droplets per minute. This study provides a high-throughput platform for the analysis and screening of amino acid-producing microorganisms.
出处 《生物工程学报》 CAS CSCD 北大核心 2014年第1期139-146,共8页 Chinese Journal of Biotechnology
基金 中国科学院科研装备研制项目(No. YZ201153) 国家自然科学基金(Nos. 21206162 21205134)资助~~
关键词 微流控芯片 高通量筛选 微液滴 稳定性 扩散性 microfluidic chip, high throughput screening, micro-droplet, stability, diffusivity
  • 相关文献

参考文献22

  • 1Parekh S,Vinci VA,Strobel RJ. Improvement of microbial strains and fermentation processes[J].{H}Applied Microbiology and Biotechnology,2000,(3):287-301.
  • 2Olsen M,Iverson B,Georgiou G. High-throughput screening of enzyme libraries[J].{H}Current Opinion in Biotechnology,2000,(4):331-337.doi:10.1016/S0958-1669(00)00108-7.
  • 3Baret JC,Miller O J,Taly V. Fluorescence-activated droplet sorting(FADS):efficient microfluidic cell sorting based on enzymatic activity[J].{H}Lab on a Chip,2009,(13):1850-1858.
  • 4林炳承;秦建华.微流控芯片实验室[M]{H}北京:科学出版社,2006.
  • 5King KR,Wang SH,Irimia D. A highthroughput microfluidic real-time gene expression living cell array[J].{H}Lab on a Chip,2007,(1):77-85.
  • 6White AK,Vanlnsberghe M,Hamidi M. High-throughput microfluidic single-cell RT-qPCR[J].{H}Proceedings of the National Academy of Sciences(USA),2011,(34):13999-14004.
  • 7Courtois F,Olguin LF,Whyte G. Controlling the retention of small molecules in emulsion microdroplets for use in cell-based assays[J].{H}Analytical Chemistry,2009,(8):3008-3016.doi:10.1021/ac802658n.
  • 8Teh SY,Lin R,Hung LH. Droplet microfluidics[J].{H}Lab on a Chip,2008,(2):198-220.
  • 9Umbanhowar PB,Prasad V,Weitz DA. Monodisperse emulsion generation via drop break off in a coflowing stream[J].{H}LANGMUIR,2000,(2):347-351.doi:10.1021/la990101e.
  • 10Agresti J J,Antipov E,Abate AR. Ultrahigh-throughput screening in drop-based microfluidics for directed evolution[J].{H}Proceedings of the National Academy of Sciences(USA),2010,(9):4004-4009.doi:10.1073/pnas.0910781107.

二级参考文献156

  • 1许宝建,金庆辉,赵建龙.基于多层SU-8结构的微喷阵列芯片的制作与应用研究[J].功能材料与器件学报,2006,12(5):377-382. 被引量:3
  • 2Qin D,Xia Y N,Rogers J A,Jackman R J,Zhao X M,Whitesides G M.Top.Curr.Chem.,1998,194:1-20.
  • 3Ye N N,Qin J H,Shi W W,Liu X,Lin B C.Lab.Chip,2007,7(12):1696-1704.
  • 4Luo C X,Zhu X J,Yu T,Luo X J,Ouyang Q,Ji H,Chen Y.Biotechnol.Bioeng.,2008,101(1):190-195.
  • 5Tan H Y,Loke W K,Tan Y T,Nguyen N T.Lab.Chip,2008,8(6):885-891.
  • 6Dittrich P S,Manz A.Nature Rev.Drug Discov.,2006,5(3):210-218.
  • 7Ma B,Zhang G H,Qin J H,Lin B C.Lab.Chip,2009,9(2):232-238.
  • 8Cheng H,Huang W H,Chen R S,Wang Z L,Cheng J K.Electrophoresis,2007,28(10):1579-1586.
  • 9Wang L,Zhu J,Deng C,Xing W L,Cheng J.Lab.Chip,2008,8(6):872-878.
  • 10Inoue I,Wakamoto Y,Moriguchi H,Okano K,Yasuda K.Lab.Chip,2001,1(1):50-55.

共引文献42

同被引文献32

引证文献5

二级引证文献20

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部