A pump-free membrane-controlled perfusion microfluidic platform

被引:11
作者
Goral, Vasiliy N. [1 ]
Tran, Elizabeth [1 ]
Yuen, Po Ki [1 ]
机构
[1] Corning Inc, Sci & Technol, Corning, NY 14831 USA
关键词
CELL-CULTURE; LAMINAR-FLOW; ARRAY; CHANNELS; SYSTEM;
D O I
10.1063/1.4930120
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this article, we present a microfluidic platform for passive fluid pumping for pump-free perfusion cell culture, cell-based assay, and chemical applications. By adapting the passive membrane-controlled pumping principle from the previously developed perfusion microplate, which utilizes a combination of hydrostatic pressure generated by different liquid levels in the wells and fluid wicking through narrow strips of a porous membrane connecting the wells to generate fluid flow, a series of pump-free membrane-controlled perfusion microfluidic devices was developed and their use for pump-free perfusion cell culture and cell-based assays was demonstrated. Each pump-free membrane-controlled perfusion microfluidic device comprises at least three basic components: an open well for generating fluid flow, a micron-sized deep chamber/channel for cell culture or for fluid connection, and a wettable porous membrane for controlling the fluid flow. Each component is fluidically connected either by the porous membrane or by the micron-sized deep chamber/channel. By adapting and incorporating the passive membrane-controlled pumping principle into microfluidic devices, all the benefits of microfluidic technologies, such as small sample volumes, fast and efficient fluid exchanges, and fluid properties at the micro-scale, can be fully taken advantage of with this pump-free membrane-controlled perfusion microfluidic platform. (C) 2015 AIP Publishing LLC.
引用
收藏
页数:11
相关论文
共 20 条
[1]   Microfluidic array for three-dimensional perfusion culture of human mammary epithelial cells [J].
Chen, Shin-Yi Cindy ;
Hung, Paul J. ;
Lee, Philip J. .
BIOMEDICAL MICRODEVICES, 2011, 13 (04) :753-758
[2]   Characterization of limiting factors in laminar flow-based membraneless microfuel cells [J].
Choban, ER ;
Waszczuk, P ;
Kenis, PJA .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2005, 8 (07) :A348-A352
[3]   Exploitation of physical and chemical constraints for three-dimensional microtissue construction in microfluidics [J].
Choudhury, Deepak ;
Mo, Xuejun ;
Iliescu, Ciprian ;
Tan, Loo Ling ;
Tong, Wen Hao ;
Yu, Hanry .
BIOMICROFLUIDICS, 2011, 5 (02)
[4]   Multi-cellular 3D human primary liver cell culture elevates metabolic activity under fluidic flow [J].
Esch, Mandy B. ;
Prot, Jean-Matthieu ;
Wang, Ying I. ;
Miller, Paula ;
Llamas-Vidales, Jose Ricardo ;
Naughton, Brian A. ;
Applegate, Dawn R. ;
Shuler, Michael L. .
LAB ON A CHIP, 2015, 15 (10) :2269-2277
[5]   A continuous perfusion microplate for cell culture [J].
Goral, Vasiliy N. ;
Zhou, Chunfeng ;
Lai, Fang ;
Yuen, Po Ki .
LAB ON A CHIP, 2013, 13 (06) :1039-1043
[6]  
Goral VN, 2010, LAB CHIP, V10, P3380, DOI [10.1039/c0lc00135j, 10.1039/c01c00135j]
[7]   A novel high aspect ratio microfluidic design to provide a stable and uniform microenvironment for cell growth in a high throughput mammalian cell culture array [J].
Hung, PJ ;
Lee, PJ ;
Sabounchi, P ;
Aghdam, N ;
Lin, R ;
Lee, LP .
LAB ON A CHIP, 2005, 5 (01) :44-48
[8]   A Cell Programmable Assay (CPA) chip [J].
Ju, Jongil ;
Warrick, Jay ;
Beebe, David J. .
LAB ON A CHIP, 2010, 10 (16) :2071-2076
[9]   Theoretical analysis of molecular diffusion in pressure-driven laminar flow in microfluidic channels [J].
Kamholz, AE ;
Yager, P .
BIOPHYSICAL JOURNAL, 2001, 80 (01) :155-160
[10]   Cell-free protein expression in a microchannel array with passive pumping [J].
Khnouf, Ruba ;
Beebe, David J. ;
Fan, Z. Hugh .
LAB ON A CHIP, 2009, 9 (01) :56-61