PubMed Health⌕ Search

PubMed · 16175254

On-line coupling of a microelectrode array equipped poly(dimethylsiloxane) microchip with an integrated graphite electrospray emitter for electrospray ionisation mass spectrometry.

Abstract

A novel method for the manufacturing of microchips for on-chip combinations of electrochemistry (EC) and sheathless electrospray ionisation mass spectrometry (ESI-MS) is described. The technique, which does not require access to clean-room facilities, is based on the incorporation of an array of gold microcoil electrodes into a poly(dimethylsiloxane)(PDMS) microflow channel equipped with an integrated graphite based sheathless ESI emitter. Electrochemical measurements, which were employed to determine the electroactive area of the electrodes and to test the microchips, show that the manufacturing process was reproducible and that the important interelectrode distance in the electrochemical cell could to be adequately controlled. The EC-ESI-MS device was evaluated based on the ESI-MS detection of the oxidation products of dopamine. The results demonstrate that the present on-chip approach enables full potentiostatic control of the electrochemical cell and the attainment of very short transfer times between the electrochemical cell and the electrospray emitter. The transfer times were 0.6 and 1.2 s for flow rates of 1.0 and 0.5 microL min(-1), respectively, while the electrochemical conversion efficiency of the electrochemical cell was found to be 30% at a flow rate of 0.5 microL min(-1). To decouple the electrochemical cell from the ESI-MS high voltage and to increase the user-friendliness, the on-line electrochemistry-ESI-MS experiments were performed using a wireless Bluetooth battery-powered instrument with the chip floating at the potential induced by the ESI high voltage. The described on-chip EC-ESI-MS device can be used for fundamental electrochemical investigations as well as for applications based on the use of electrochemically controlled sample pretreatment, preconcentration and ionisation steps prior to ESI-MS.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Gustav Liljegren, Andreas Dahlin, Camilla Zettersten, Jonas Bergquist, Leif Nyholm. 2005-08-10. On-line coupling of a microelectrode array equipped poly(dimethylsiloxane) microchip with an integrated graphite electrospray emitter for electrospray ionisation mass spectrometry.. https://doi.org/10.1039/b506289f

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Study of on-line monitoring of lactate based on optical fibre sensor and in-channel mixing mechanism.

A PDMS-based microfluidic device with integrated optical fibres was developed for online monitoring of lactate. The detection is based on the optical adsorption of the colour solution formed by in-channel mixing of sample and reagent solutions. Computational Fluid Dynamics (CFD) simulation and kinetic study of the colour development were conducted to determine the minimum channel length and optimum residential time for homogenous mixing and maximum optical adsorption respectively. The system was proved to be able to detect lactate with good linearity (R(2)=0.98), response time of about 130 s and estimated limitation of detection (LOD) of 0.52 mM (about 47 mg/L), which is sufficient for a general online lactate detection. Due to the miniaturization of sensing system and micro-scale mixing, higher detection sensitivity (0.15 V/mM) can be realized than the mixing in lab-scale equipments (0.08 V/mM).

Dimethylpolysiloxanes↗

Glass-fiber reinforced poly(acrylate)-based sorptive materials for the enrichment of organic micropollutants from aqueous samples.

A novel and simple approach to sorptive materials for the extraction of organic compounds from environmental samples is presented. It entails the use of glass fiber fabric strips coated with a customized poly(acrylate) (PA) formulation as extraction medium. Analytes were enriched by means of shaking of the PA strip in the sample and then subsequently thermally desorbed and analyzed by GC-MS. The performance of the sorptive materials was evaluated by the enrichment of compounds with different polarities (phenols, hexachlorobenzene and hexachlorocyclohexanes) from water samples. Parameters that affect the extraction process such as pH, ionic strength of the solvent, mixing mechanism, extraction time and desorption conditions were investigated. The extraction abilities of the PA extraction medium were compared with that of commercially available poly(dimethylsiloxane) (PDMS) Twisters. The results revealed that the new material shows higher affinity for phenolic compounds presumably due to the presence of polar groups. The partition coefficients for the PA strips estimated in this work were up to 15 times higher than for the PDMS Twister, resulting in higher recoveries and lower detection limits. The method was applied for the quantification of the aforementioned compounds in contaminated surface water samples from Bitterfeld (Germany). Using both PA strips and PDMS Twisters, good agreement of the extraction data was achieved.

Dimethylpolysiloxanes↗