PDMS/glass hybrid device with a reusable carbon electrode for on-line monitoring of catecholamines using microdialysis sampling coupled to microchip electrophoresis with electrochemical detection
被引:18
作者:
Saylor, Rachel A.
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机构:
Univ Kansas, Dept Chem, Lawrence, KS 66047 USA
Univ Kansas, Ralph N Adams Inst Bioanalyt Chem, Lawrence, KS 66047 USAUniv Kansas, Dept Chem, Lawrence, KS 66047 USA
Saylor, Rachel A.
[1
,2
]
Lunte, Susan M.
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机构:
Univ Kansas, Dept Chem, Lawrence, KS 66047 USA
Univ Kansas, Ralph N Adams Inst Bioanalyt Chem, Lawrence, KS 66047 USA
Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USAUniv Kansas, Dept Chem, Lawrence, KS 66047 USA
Lunte, Susan M.
[1
,2
,3
]
机构:
[1] Univ Kansas, Dept Chem, Lawrence, KS 66047 USA
[2] Univ Kansas, Ralph N Adams Inst Bioanalyt Chem, Lawrence, KS 66047 USA
[3] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USA
On-line separations-based sensors employing microdialysis (MD) coupled to microchip electrophoresis (ME) enable the continuous monitoring of multiple analytes simultaneously. Electrochemical detection (EC) is especially amenable to on-animal systems employing MD-ME due to its ease of miniaturization. However, one of the difficulties in fabricating MD-ME-EC systems is incorporating carbon working electrodes into the device. In this paper, a novel fabrication procedure is described for the production of a PDMS/glass hybrid device that is capable of integrating hydrodynamic MD flow with ME-EC using a flow-gated interface and a pyrolyzed photoresist film carbon electrode. This fabrication method enables the reuse of carbon electrodes on a glass substrate, while still maintaining a good seal between the PDMS and glass to allow for pressure-driven MD flow. The on-line MD-ME-EC device was characterized in vitro and in vivo for monitoring analytes in the dopamine metabolic pathway. The ultimate goal is to use this device and associated instrumentation to perform on-animal, near-real time in vivo monitoring of catecholamines.