Generating Nonlinear Concentration Gradients in Microfluidic Devices for Cell Studies

被引:42
|
作者
Selimovic, Seila [2 ,3 ]
Sim, Woo Young [2 ,3 ]
Kirn, Sang Bok [2 ,3 ]
Jang, Yun Ho [2 ,3 ]
Lee, Won Gu [2 ,3 ,4 ]
Khabiry, Masoud [2 ,3 ]
Bae, Hojae [2 ,3 ]
Jambovane, Sachin [1 ]
Hong, Jong Wook [1 ]
Khademhosseini, Ali [2 ,3 ,5 ]
机构
[1] Auburn Univ, Dept Mech Engn, Wilmore Lab 275, Auburn, AL 36849 USA
[2] Harvard Univ, Ctr Biomed Engn, Dept Med, Brigham & Womens Hosp,Med Sch, Boston, MA 02115 USA
[3] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[4] Kyung Hee Univ, Dept Mech Engn, Coll Engn, Yongin 446701, Gyeonggi, South Korea
[5] Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02139 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
DIFFUSION; CHANNELS; DOCKING; CULTURE; GROWTH; ARRAYS;
D O I
10.1021/ac2001737
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We describe a microfluidic device for generating nonlinear (exponential and sigmoidal) concentration gradients, coupled with a microwell array for cell storage and analysis. The device has two inputs for coflowing multiple aqueous solutions, a main coflow channel and an asymmetrical grid of fluidic channels that allows the two solutions to combine at intersection points without fully mixing. Due to this asymmetry and diffusion of the two species in the coflow channel, varying amounts of the two solutions enter each fluidic path. This induces exponential and sigmoidal concentration gradients at low and high flow rates, respectively, making the microfluidic device versatile. A key feature of this design is that it is space saving, as it does not require multiplexing or a separate array of mixing channels. Furthermore, the gradient structure can be utilized in concert with cell experiments, to expose cells captured in microwells to various concentrations of soluble factors. We demonstrate the utility of this design to assess the viability of fibroblast cells in response to a range of hydrogen peroxide (H2O2) concentrations
引用
收藏
页码:2020 / 2028
页数:9
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