Microplatforms for Gradient Field Generation of Various Properties and Biological Applications

被引:11
作者
Kim, Sung-Hwan [1 ]
Lee, Gi-Hun [1 ]
Park, Joong Yull [1 ]
Lee, Sang-Hoon [2 ]
机构
[1] Chung Ang Univ, Coll Engn, Sch Mech Engn, Seoul 156756, South Korea
[2] Korea Univ, Coll Hlth Sci, Dept Biomed Engn, Seoul, South Korea
来源
JALA | 2015年 / 20卷 / 02期
基金
新加坡国家研究基金会;
关键词
microfluidics; lab-on-a-chip; microtechnology; fabrication; CELL-CULTURE; MICROFLUIDIC DEVICE; STEM-CELLS; IN-VITRO; CHIP; CHEMOTAXIS; SEPARATION; PLATFORM; MIGRATION; OXYGEN;
D O I
10.1177/2211068214562247
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Well-designed microfluidic platforms can be excellent tools to eliminate bottleneck problems or issues that have arisen in biological fields by providing unprecedented high-resolution control of mechanical and chemical microenvironments for cell culture. Among such microtechnologies, the precise generation of biochemical concentration gradients has been highly regarded in the biorelated scientific fields; even today, the principles and mechanisms for gradient generation continue to be refined, and the number of applications for this technique is growing. Here, we review the current status of the concentration gradient generation technologies achieved in various microplatforms and how they have been and will be applied to biological issues, particularly those that have arisen from cancer research, stem cell research, and tissue engineering. We also provide information about the advances and future challenges in the technological aspects of microscale concentration gradient generation.
引用
收藏
页码:82 / 95
页数:14
相关论文
共 85 条
[1]   A platform for assessing chemotactic migration within a spatiotemporally defined 3D microenvironment [J].
Abhyankar, Vinay V. ;
Toepke, Michael W. ;
Cortesio, Christa L. ;
Lokuta, Mary A. ;
Huttenlocher, Anna ;
Beebe, David J. .
LAB ON A CHIP, 2008, 8 (09) :1507-1515
[2]   Characterization of a membrane-based gradient generator for use in cell-signaling studies [J].
Abhyankar, VV ;
Lokuta, MA ;
Huttenlocher, A ;
Beebe, DJ .
LAB ON A CHIP, 2006, 6 (03) :389-393
[3]   The modulation of dendritic cell integrin binding and activation by RGD-peptide density gradient substrates [J].
Acharya, Abhinav P. ;
Dolgova, Natalia V. ;
Moore, Nicole M. ;
Xia, Chang-Qing ;
Clare-Salzler, Michael J. ;
Becker, Matthew L. ;
Gallant, Nathan D. ;
Keselowsky, Benjamin G. .
BIOMATERIALS, 2010, 31 (29) :7444-7454
[4]   Formation of steady-state oxygen gradients in vitro - Application to liver zonation [J].
Allen, JW ;
Bhatia, SN .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 82 (03) :253-262
[6]   An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons [J].
Brandon, EFA ;
Raap, CD ;
Meijerman, I ;
Beijnen, JH ;
Schellens, JHM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 189 (03) :233-246
[7]   Fabrication of gradient hydrogels using a microfluidics/photopolymerization process [J].
Burdick, JA ;
Khademhosseini, A ;
Langer, R .
LANGMUIR, 2004, 20 (13) :5153-5156
[8]   Semaphorin-neuropilin interactions underlying sympathetic axon responses to class III semaphorins [J].
Chen, H ;
He, ZG ;
Bagri, A ;
Tessier-Lavigne, M .
NEURON, 1998, 21 (06) :1283-1290
[9]   A hydrogel-based microfluidic device for the studies of directed cell migration [J].
Cheng, Shing-Yi ;
Heilman, Steven ;
Wasserman, Max ;
Archer, Shivaun ;
Shuler, Michael L. ;
Wu, Mingming .
LAB ON A CHIP, 2007, 7 (06) :763-769
[10]   Neurotoxic amyloid beta oligomeric assemblies recreated in microfluidic platform with interstitial level of slow flow [J].
Choi, Yoon Jung ;
Chae, Sukyung ;
Kim, Jeong Hun ;
Barald, Kate F. ;
Park, Joong Yull ;
Lee, Sang-Hoon .
SCIENTIFIC REPORTS, 2013, 3