A Cell Programmable Assay (CPA) chip

被引:9
作者
Ju, Jongil
Warrick, Jay
Beebe, David J. [1 ]
机构
[1] Univ Wisconsin, Dept Biomed Engn, Madison, WI 53705 USA
关键词
ON-A-CHIP; CULTURE; SURFACE; ARRAY; FLOW; MICROSYSTEMS; EXPRESSION; SYSTEM; PCR; DNA;
D O I
10.1039/c005103a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This article describes two kinds of "Cell Programmable Assay'' (CPA) chips that utilize passive pumping for the culture and autonomous staining of cells to simply common protocols. One is a single timer channel CPA (sCPA) chip that has one timer channel and one main channel containing a cell culture chamber. The sCPA is used to culture and stain cells using Hoechst nuclear staining dye (a 2 step staining process). The other is a dual timer channel CPA (dCPA) chip that has two timer channels and one main channel with a chamber for cell culture. The dCPA is used here to culture, fix, permeablize, and stain cells using DAPI. The additional timer channel of the dCPA chip allows for automation of 3 steps. The CPA chips were successfully evaluated using HEK 293 cells. In addition, we provide a simplified equation for tuning or redesigning CPA chips to meet the needs of a variety of protocols that may require different timings. The equation is easy to use as it only depends upon the dimensions of microchannel and the volume of the reagent drops. The sCPA and dCPA chips can be readily modified to apply to a wide variety of common cell culture methods and procedures.
引用
收藏
页码:2071 / 2076
页数:6
相关论文
共 32 条
[1]   Flow rate analysis of a surface tension driven passive micropump [J].
Berthier, Erwin ;
Beebe, David J. .
LAB ON A CHIP, 2007, 7 (11) :1475-1478
[2]   Nanoparticles with Raman spectroscopic fingerprints for DNA and RNA detection [J].
Cao, YWC ;
Jin, RC ;
Mirkin, CA .
SCIENCE, 2002, 297 (5586) :1536-1540
[3]   Lab-on-a-chip: microfluidics in drug discovery [J].
Dittrich, PS ;
Manz, A .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (03) :210-218
[4]   Cellular observations enabled by microculture: paracrine signaling and population demographics [J].
Domenech, Maribella ;
Yu, Hongmei ;
Warrick, Jay ;
Badders, Nisha M. ;
Meyvantsson, Ivar ;
Alexander, Caroline M. ;
Beebe, David J. .
INTEGRATIVE BIOLOGY, 2009, 1 (03) :267-274
[5]   Cells on chips [J].
El-Ali, Jamil ;
Sorger, Peter K. ;
Jensen, Klavs F. .
NATURE, 2006, 442 (7101) :403-411
[6]   Versatile, fully automated, microfluidic cell culture system [J].
Gomez-Sjoeberg, Rafael ;
Leyrat, Anne A. ;
Pirone, Dana M. ;
Chen, Christopher S. ;
Quake, Stephen R. .
ANALYTICAL CHEMISTRY, 2007, 79 (22) :8557-8563
[7]   An integrated cell culture lab on a chip: modular microdevices for cultivation of mammalian cells and delivery into microfluidic microdroplets [J].
Hufnagel, Hansjoerg ;
Huebner, Ansgar ;
Guelch, Carina ;
Guese, Katharina ;
Abell, Chris ;
Hollfelder, Florian .
LAB ON A CHIP, 2009, 9 (11) :1576-1582
[8]   Continuous perfusion microfluidic cell culture array for high-throughput cell-based assays [J].
Hung, PJ ;
Lee, PJ ;
Sabounchi, P ;
Lin, R ;
Lee, LP .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 89 (01) :1-8
[9]   Three-dimensional micro-channel fabrication in polydimethylsiloxane (PDMS) elastomer [J].
Jo, BH ;
Van Lerberghe, LM ;
Motsegood, KM ;
Beebe, DJ .
JOURNAL OF MICROELECTROMECHANICAL SYSTEMS, 2000, 9 (01) :76-81
[10]   Backward flow in a surface tension driven micropump [J].
Ju, Jongil ;
Park, Joong Yull ;
Kim, Kyung Chun ;
Kim, Hyundong ;
Berthier, Erwin ;
Beebe, David J. ;
Lee, Sang-Hoon .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2008, 18 (08)