Measurement of electroosmotic flow in plastic imprinted microfluid devices and the effect of protein adsorption on flow rate

被引:161
作者
Locascio, LE [1 ]
Perso, CE
Lee, CS
机构
[1] Natl Inst Stand & Technol, Div Analyt Chem, Gaithersburg, MD 20899 USA
[2] Univ Maryland, Dept Chem & Biochem, College Pk, MD 20742 USA
关键词
electroosmotic flow; instrumentation; imprinted polymers; polymer microfluid devices; proteins;
D O I
10.1016/S0021-9673(99)00774-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Several commercially available plastic materials were used as substrates in Phe fabrication of microfluid channels for biochemical analysis. Protocols for fabrication using the wire-imprinting method are reported for polystyrene, polymethylmethacrylate and a copolyester material. Channel sealing was accomplished by low-temperature bonding of a substrate of similar material; therefore, each channel was composed of a single material on all sides. The electroosmotic flow in 25-mu m imprinted channels was evaluated for each substrate material. The copolyester material exhibited the highest electroosmotic flow mobility of 4.3 . 10(-4) cm(2) V-1 s(-1) which is similar to that previously reported for fused-silica capillaries. Polystyrene exhibited the lowest electroosmotic flow mobility of 1.8 . 10(-4) cm(2) V-1 s(-1). Plots of linear velocity versus applied electric field strength were linear from 100 V cm(-1) to 500 V cm(-1) indicating that heat dissipation is effective for all substrates in this range. Electroosmotic flow was reevaluated in the plastic channels following incubation in antibody solution to access the non-specific binding characteristics of a common biochemical reagent onto the substrate materials. All materials tested showed a high degree of non-specific adsorption of IgG as indicated by a decrease in the electroosmotic flow mobility in post-incubation testing. Published by Elsevier Science B.V.
引用
收藏
页码:275 / 284
页数:10
相关论文
共 22 条
[1]  
Bayer H, 1996, J MICROCOLUMN SEP, V8, P479
[2]  
Becker H, 2000, MESA MG, P253
[3]  
Boer G., 1998, MICROTOTAL ANAL SYST, P53
[4]  
BOONE TD, 1998, SOL STAT SENS ACT WO, P87
[5]   An integrated nanoliter DNA analysis device [J].
Burns, MA ;
Johnson, BN ;
Brahmasandra, SN ;
Handique, K ;
Webster, JR ;
Krishnan, M ;
Sammarco, TS ;
Man, PM ;
Jones, D ;
Heldsinger, D ;
Mastrangelo, CH ;
Burke, DT .
SCIENCE, 1998, 282 (5388) :484-487
[6]   Clinical potential of microchip capillary electrophoresis systems [J].
Colyer, CL ;
Tang, T ;
Chiem, N ;
Harrison, DJ .
ELECTROPHORESIS, 1997, 18 (10) :1733-1741
[7]   Integrated capillary electrophoresis on flexible silicone microdevices: Analysis of DNA restriction fragments and detection of single DNA molecules on microchips [J].
Effenhauser, CS ;
Bruin, GJM ;
Paulus, A ;
Ehrat, M .
ANALYTICAL CHEMISTRY, 1997, 69 (17) :3451-3457
[8]  
Ford SM, 1998, J MICROCOLUMN SEP, V10, P413, DOI 10.1002/(SICI)1520-667X(1998)10:5<413::AID-MCS4>3.0.CO
[9]  
2-J
[10]   CURRENT-MONITORING METHOD FOR MEASURING THE ELECTROOSMOTIC FLOW-RATE IN CAPILLARY ZONE ELECTROPHORESIS [J].
HUANG, XH ;
GORDON, MJ ;
ZARE, RN .
ANALYTICAL CHEMISTRY, 1988, 60 (17) :1837-1838