Monolithic porous polymer for on-chip solid-phase extraction and preconcentration prepared by photoinitiated in situ polymerization within a microfluidic device

被引:327
作者
Yu, C
Davey, MH
Svec, F
Fréchet, JMJ [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] EO Lawrence Berkeley Natl Lab, Div Mat Sci, Berkeley, CA 94720 USA
关键词
D O I
10.1021/ac0106288
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Monolithic porous polymers have been prepared by photoinitiated polymerization within the channels of a microfluidic device and used for on-chip solid-phase extraction and preconcentration. The preparation of the monolithic material with hydrophobic and ionizable surface chemistries is easily achieved by copolymerization of butyl methacrylate with ethylene dimethacrylate, or 2-hydroxyethyl methacrylate and [2-(methacryloyloxy)ethyl]trimethylammonium. chloride with ethylene dimethacrylate, respectively. The porous properties, and consequently the flow resistance, of the monolithic device are controlled by the use of a mixture of hexane and methanol as a porogenic mixture. This mixture was designed to meet the specific requirements for pore formation within macroporous monoliths useful in the microfluidic formats. The low flow resistance enables high flow rates of up to 10 muL/min, which corresponds to a linear flow velocity of 50 mm/s and far exceeds the flow velocities typical of the common analytical microchips. The function of the monolithic concentration device was first demonstrated using very dilute solutions of Coumarin 519. The performance in a more realistic application was then demonstrated with the enrichment of a hydrophobic tetrapeptide and also of green fluorescent protein for which an increase in concentration by a factor as high as 10(3) was achieved.
引用
收藏
页码:5088 / 5096
页数:9
相关论文
共 59 条
[21]  
Kutter JP, 2000, J MICROCOLUMN SEP, V12, P93, DOI 10.1002/(SICI)1520-667X(2000)12:2<93::AID-MCS5>3.0.CO
[22]  
2-P
[23]   Solvent-programmed microchip open-channel electrochromatography [J].
Kutter, JP ;
Jacobson, SC ;
Matsubara, N ;
Ramsey, JM .
ANALYTICAL CHEMISTRY, 1998, 70 (15) :3291-3297
[24]   Single-molecule DNA amplification and analysis in an integrated microfluidic device [J].
Lagally, ET ;
Medintz, I ;
Mathies, RA .
ANALYTICAL CHEMISTRY, 2001, 73 (03) :565-570
[25]   Chiral monolithic columns for enantioselective capillary electrochromatography prepared by copolymerization of a monomer with quinidine functionality.: 1.: Optimization of polymerization conditions, porous properties, and chemistry of the stationary phase [J].
Lämmerhofer, M ;
Peters, EC ;
Yu, C ;
Svec, F ;
Fréchet, JMJ ;
Lindner, W .
ANALYTICAL CHEMISTRY, 2000, 72 (19) :4614-4622
[26]   Separation and identification of peptides from gel-isolated membrane proteins using a microfabricated device for combined capillary electrophoresis/nanoelectrospray mass spectrometry [J].
Li, JJ ;
Kelly, JF ;
Chemushevich, I ;
Harrison, DJ ;
Thibault, P .
ANALYTICAL CHEMISTRY, 2000, 72 (03) :599-609
[27]   Trace enrichment of phenolic compounds from aqueous samples by dynamic ion-exchange solid-phase extraction [J].
Li, NQ ;
Lee, HK .
ANALYTICAL CHEMISTRY, 1997, 69 (24) :5193-5199
[28]   Sample preparation based on dynamic ion-exchange solid phase extraction for GC/MS analysis of acidic herbicides in environmental waters [J].
Li, NQ ;
Lee, HK .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3077-3084
[29]   Electrophoretic separation of proteins on a microchip with noncovalent, postcolumn labeling [J].
Liu, YJ ;
Foote, RS ;
Jacobson, SC ;
Ramsey, RS ;
Ramsey, JM .
ANALYTICAL CHEMISTRY, 2000, 72 (19) :4608-4613
[30]   Techniques for the optimization of proteomic strategies based on head column stacking capillary electrophoresis [J].
Locke, S ;
Figeys, D .
ANALYTICAL CHEMISTRY, 2000, 72 (13) :2684-2689