Rapid prototyping of thermoset polyester microfluidic devices

被引:81
作者
Fiorini, GS [1 ]
Lorenz, RM [1 ]
Kuo, JS [1 ]
Chiu, DT [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
关键词
D O I
10.1021/ac0498922
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper presents a simple procedure for the fabrication of thermoset polyester (TPE) microfluidic systems and discusses the properties of the final devices. TPE chips are fabricated in less than 3 h by casting TPE resin directly on a lithographically patterned (SU-8) silicon master. Thorough curing of the devices is obtained through the combined use of ultraviolet light and heat, as both an ultraviolet and a thermal initiator are employed in the resin mixture. Features on the order of micrometers and greater are routinely reproduced using the presented procedure, including complex designs and multilayer features. The surface of TPE was characterized using contact angle measurements and X-ray photoelectron spectroscopy (XPS). Following oxygen plasma treatment, the hydrophilicity of the surface of TPE increases (determined by contact angle measurements) and the proportion of oxygen-containing functional groups also increases (determined by XPS), which indicates a correlated increase in the charge density on the surface. Native TPE microchannels support electroosmotic flow (EOF) toward the cathode, with an average electroosmotic mobility of 1.3 x 10(-4) cm(2) V-1 s(-1) for a 50-mum square channel (20 mM borate at pH 9); following plasma treatment (5 min at 30 W and 0.3 mbar), EOF is enhanced by a factor of 2. This enhancement of the EOF from plasma treatment is stable for days, with no significant decrease noted during the 5-day period that we monitored. Using plasma-treated TPE microchannels, we demonstrate the separation of a mixture of fluorescein-tagged amino acids (glycine, glutamic acid, aspartic acid). TPE devices are up to 90% transparent (for similar to2-mm-thick sample) to visible light (400-800 nm). The compatibility of TPE with a wide range of solvents was tested over a 24-h period, and the material performed well with acids, bases, alcohols, cyclohexane, n-heptane, and toluene but not with chlorinated solvents (dichloromethane, chloroform).
引用
收藏
页码:4697 / 4704
页数:8
相关论文
共 82 条
  • [1] Fabrication of topologically complex three-dimensional microfluidic systems in PDMS by rapid prototyping
    Anderson, JR
    Chiu, DT
    Jackman, RJ
    Cherniavskaya, O
    McDonald, JC
    Wu, HK
    Whitesides, SH
    Whitesides, GM
    [J]. ANALYTICAL CHEMISTRY, 2000, 72 (14) : 3158 - 3164
  • [2] Micro total analysis systems. 2. Analytical standard operations and applications
    Auroux, PA
    Iossifidis, D
    Reyes, DR
    Manz, A
    [J]. ANALYTICAL CHEMISTRY, 2002, 74 (12) : 2637 - 2652
  • [3] Becker H, 2000, ELECTROPHORESIS, V21, P12, DOI 10.1002/(SICI)1522-2683(20000101)21:1<12::AID-ELPS12>3.3.CO
  • [4] 2-Z
  • [5] Polymer microfluidic devices
    Becker, H
    Locascio, LE
    [J]. TALANTA, 2002, 56 (02) : 267 - 287
  • [6] Becker H, 1999, SENSOR MATER, V11, P297
  • [7] Microfluidic tectonics: A comprehensive construction platform for microfluidic systems
    Beebe, DJ
    Moore, JS
    Yu, Q
    Liu, RH
    Kraft, ML
    Jo, BH
    Devadoss, C
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) : 13488 - 13493
  • [8] Functional hydrogel structures for autonomous flow control inside microfluidic channels
    Beebe, DJ
    Moore, JS
    Bauer, JM
    Yu, Q
    Liu, RH
    Devadoss, C
    Jo, BH
    [J]. NATURE, 2000, 404 (6778) : 588 - +
  • [9] Physics and applications of microfluidics in biology
    Beebe, DJ
    Mensing, GA
    Walker, GM
    [J]. ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, 2002, 4 : 261 - 286
  • [10] Micromosaic immunoassays
    Bernard, A
    Michel, B
    Delamarche, E
    [J]. ANALYTICAL CHEMISTRY, 2001, 73 (01) : 8 - 12