Fabrication of a circular PDMS microchannel for constructing a three-dimensional endothelial cell layer

被引:52
作者
Choi, Jong Seob
Piao, Yunxian
Seo, Tae Seok [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Taejon 305701, South Korea
关键词
Polydimethylsiloxane; Circular microchannels; Cell culture; Reflow of photoresist; Human umbilical vein endothelial cells; CROSS-SECTIONS; ADHESION; CULTURE; MICROFLUIDICS; CHANNELS; GLASS; FLOW; RHO;
D O I
10.1007/s00449-013-0961-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We describe a simple and efficient fabrication method for generating microfluidic channels with a circular cross-sectional geometry by exploiting the reflow phenomenon of a thick positive photoresist. Initial rectangular shaped positive photoresist micropatterns on a silicon wafer, which were fabricated by a conventional photolithography process, were converted into a half-circular shape by tuning the temperature to around 105 A degrees C. Through optimization of the reflow conditions, we could obtain a perfect circular micropattern of the positive photoresist, and control the diameter in a range from 100 to 400 mu m. The resultant convex half-circular photoresist was used as a template for fabricating a concave polydimethylsiloxane (PDMS) through a replica molding process, and a circular PDMS microchannel was produced by bonding two half-circular PDMS layers. A variety of channel dimensions and patterns can be easily prepared, including straight, S-curve, X-, Y-, and T-shapes to mimic an in vivo vascular network. To form an endothelial cell layer, we cultured primary human umbilical vein endothelial cells inside circular PDMS microchannels, and demonstrated successful cell adhesion, proliferation, and alignment along the channel.
引用
收藏
页码:1871 / 1878
页数:8
相关论文
共 34 条
[1]   HMEC-1 - ESTABLISHMENT OF AN IMMORTALIZED HUMAN MICROVASCULAR ENDOTHELIAL-CELL LINE [J].
ADES, EW ;
CANDAL, FJ ;
SWERLICK, RA ;
GEORGE, VG ;
SUMMERS, S ;
BOSSE, DC ;
LAWLEY, TJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (06) :683-690
[2]   Micro total analysis systems. 2. Analytical standard operations and applications [J].
Auroux, PA ;
Iossifidis, D ;
Reyes, DR ;
Manz, A .
ANALYTICAL CHEMISTRY, 2002, 74 (12) :2637-2652
[3]   Surface tension, adhesion and wetting of materials for photolithographic process [J].
Bauer, J ;
Drescher, G ;
Illig, M .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY B, 1996, 14 (04) :2485-2492
[4]   Polymer microfluidic devices [J].
Becker, H ;
Locascio, LE .
TALANTA, 2002, 56 (02) :267-287
[5]   Functional endothelialized microvascular networks with circular cross-sections in a tissue culture substrate [J].
Borenstein, Jeffrey T. ;
Tupper, Malinda M. ;
Mack, Peter J. ;
Weinberg, Eli J. ;
Khalil, Ahmad S. ;
Hsiao, James ;
Garcia-Cardena, Guillermo .
BIOMEDICAL MICRODEVICES, 2010, 12 (01) :71-79
[6]   Lab-on-a-chip: microfluidics in drug discovery [J].
Dittrich, PS ;
Manz, A .
NATURE REVIEWS DRUG DISCOVERY, 2006, 5 (03) :210-218
[7]   A circular cross-section PDMS microfluidics system for replication of cardiovascular flow conditions [J].
Fiddes, Lindsey K. ;
Raz, Neta ;
Srigunapalan, Suthan ;
Tumarkan, Ethan ;
Simmons, Craig A. ;
Wheeler, Aaron R. ;
Kumacheva, Eugenia .
BIOMATERIALS, 2010, 31 (13) :3459-3464
[8]   Rapid prototyping of microstructures with bell-shaped cross-sections and its application to deformation-based microfluidic valves [J].
Futai, N ;
Gu, W ;
Takayama, S .
ADVANCED MATERIALS, 2004, 16 (15) :1320-+
[9]   FUNCTIONAL-HETEROGENEITY OF VASCULAR ENDOTHELIAL-CELLS - COMMENTARY [J].
GERRITSEN, ME .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (17) :2701-2711
[10]   Deep wet etching of fused silica glass for hollow capillary optical leaky waveguides in microfluidic devices [J].
Grosse, A ;
Grewe, M ;
Fouckhardt, H .
JOURNAL OF MICROMECHANICS AND MICROENGINEERING, 2001, 11 (03) :257-262