Cell culture in microfluidic systems has primarily been conducted in devices comprised of polydimethylsiloxane (PDMS) or other elastomers. As polystyrene (PS) is the most characterized and commonly used substrate material for cell culture, microfluidic cell culture would ideally be conducted in PS-based microsystems that also enable tight control of perfusion and hydrodynamic conditions, which are especially important for culture of vascular cell types. Here, we report a simple method to prototype perfusable PS microfluidics for endothelial cell culture under flow that can be fabricated using standard lithography and wet laboratory equipment to enable stable perfusion at shear stresses up to 300 dyn/cm2 and pumping pressures up to 26 kPa for at least 100 h. This technique can also be extended to fabricate perfusable hybrid PS-PDMS microfluidics of which one application is for increased efficiency of viral transduction in non-adherent suspension cells by leveraging the high surface area to volume ratio of microfluidics and adhesion molecules that are optimized for PS substrates. These biologically compatible microfluidic devices can be made more accessible to biological-based laboratories through the outsourcing of lithography to various available microfluidic foundries.
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July 2014
Research Article|
July 30 2014
Simplified prototyping of perfusable polystyrene microfluidics
Reginald Tran;
Reginald Tran
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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Byungwook Ahn;
Byungwook Ahn
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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David R. Myers;
David R. Myers
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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Yongzhi Qiu;
Yongzhi Qiu
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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Yumiko Sakurai;
Yumiko Sakurai
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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Robert Moot;
Robert Moot
5Graduate Program in Molecular and Systems Pharmacology, Laney Graduate School,
Emory University, Atlanta
, Georgia 30322, USA
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Emma Mihevc;
Emma Mihevc
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
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H. Trent Spencer;
H. Trent Spencer
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
5Graduate Program in Molecular and Systems Pharmacology, Laney Graduate School,
Emory University, Atlanta
, Georgia 30322, USA
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Christopher Doering;
Christopher Doering
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
5Graduate Program in Molecular and Systems Pharmacology, Laney Graduate School,
Emory University, Atlanta
, Georgia 30322, USA
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Wilbur A. Lam
Wilbur A. Lam
a)
1Aflac Cancer Center and Blood Disorders Service, Department of Pediatrics,
Emory University, Atlanta
, Georgia 30322, USA
2The Wallace H. Coulter Department of Biomedical Engineering,
Georgia Institute of Technology and Emory University, Atlanta
, Georgia 30332, USA
3Parker H. Petit Institute of Bioengineering and Bioscience,
Georgia Institute of Technology, Atlanta
, Georgia 30332, USA
4Winship Cancer Institute,
Emory University, Atlanta
, Georgia 30322, USA
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a)
E-mail: [email protected]
Biomicrofluidics 8, 046501 (2014)
Article history
Received:
May 15 2014
Accepted:
July 21 2014
Citation
Reginald Tran, Byungwook Ahn, David R. Myers, Yongzhi Qiu, Yumiko Sakurai, Robert Moot, Emma Mihevc, H. Trent Spencer, Christopher Doering, Wilbur A. Lam; Simplified prototyping of perfusable polystyrene microfluidics. Biomicrofluidics 1 July 2014; 8 (4): 046501. https://doi.org/10.1063/1.4892035
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