Microfluidic chip for low-flow push-pull perfusion sampling in vivo with on-line analysis of amino acids

被引:73
作者
Cellar, NA
Burns, ST
Meiners, JC
Chen, H
Kennedy, RT [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1021/ac0510033
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Multilayer soft lithography was used to prepare a poly(dimethyisiloxane) microfluidic chip that allows for in vivo sampling of amino acid neurotransmitters by low-flow push-pull perfusion. The chip incorporates a pneumatically actuated peristaltic pump to deliver artificial cerebrospinal fluid to a push-pull perfusion probe, pull sample from the probe, perform on-line derivatization with o-phthaldialdehyde, and push derivatized amino acids into the flow-gated injector of a high-speed capillary electrophoresis-laser-induced fluorescence instrument. Peristalsis was achieved by sequential actuation of six, 200 mu m wide by 15 mu m high control valves that drove fluid through three fluidic channels of equal dimensions. Electropherograms with 100 000 theoretical plates were acquired at similar to 20-s intervals. Relative standard deviations of peak heights were 4% in vitro, and detection limits for the excitatory amino acids were similar to 60 nM. For in vivo measurements, push-pull probes were implanted in the striatum of anesthetized rats and amino acid concentrations were monitored while sampling at 50 nL/min. o-Phosphorylethanolamine, glutamate, aspartate, taurine, glutamine, serine, and glycine were all detected with stable peak heights observed for over 4 h with relative standard deviations of 10% in vivo. Basal concentrations of glutamate were 1.9 +/- 0.6 mu M (n = 4) in good agreement with similar methods. Monitoring of dynamic changes of neurotransmitters resulting from 10-min applications of 70 mM K+ through the push channel of the pump was demonstrated. The combined system allows temporal resolution for multianalyte monitoring of similar to 45 s with spatial resolution 65-fold better than conventional microdialysis probe with 4-mm length. The system demonstrates the feasibility of sampling from a complex microenvironment with transfer to a microfluidic device for on-line analysis.
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收藏
页码:7067 / 7073
页数:7
相关论文
共 29 条
[1]   ORTHO-PHTHALALDEHYDE DERIVATIVES OF AMINES FOR HIGH-SPEED LIQUID-CHROMATOGRAPHY ELECTROCHEMISTRY [J].
ALLISON, LA ;
MAYER, GS ;
SHOUP, RE .
ANALYTICAL CHEMISTRY, 1984, 56 (07) :1089-1096
[2]  
Bowser MT, 2001, ELECTROPHORESIS, V22, P3668, DOI 10.1002/1522-2683(200109)22:17<3668::AID-ELPS3668>3.0.CO
[3]  
2-M
[4]   Robust interconnects and packaging for microfluidic elastomeric chips [J].
Chen, H ;
Acharya, D ;
Gajraj, A ;
Meiners, JC .
ANALYTICAL CHEMISTRY, 2003, 75 (19) :5287-5291
[5]   Monitoring D-serine dynamics in the rat brain using online microdialysis-capillary electrophoresis [J].
Ciriacks, CM ;
Bowser, MT .
ANALYTICAL CHEMISTRY, 2004, 76 (22) :6582-6587
[6]   Analytical considerations for microdialysis sampling [J].
Davies, MI ;
Cooper, JD ;
Desmond, SS ;
Lunte, CE ;
Lunte, SM .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 45 (2-3) :169-188
[7]   Rapid prototyping of microfluidic systems in poly(dimethylsiloxane) [J].
Duffy, DC ;
McDonald, JC ;
Schueller, OJA ;
Whitesides, GM .
ANALYTICAL CHEMISTRY, 1998, 70 (23) :4974-4984
[8]   An integrated microfabricated cell sorter [J].
Fu, AY ;
Chou, HP ;
Spence, C ;
Arnold, FH ;
Quake, SR .
ANALYTICAL CHEMISTRY, 2002, 74 (11) :2451-2457
[9]  
HerreraMarschitz M, 1996, J NEUROCHEM, V66, P1726
[10]   Integrated nanoliter systems [J].
Hong, JW ;
Quake, SR .
NATURE BIOTECHNOLOGY, 2003, 21 (10) :1179-1183