PubMed Health⌕ Search

PubMed · 11700719

Field-effect flow control in a polydimethylsiloxane-based microfluidic system.

Abstract

The application of the field-effect for direct control of electroosmosis in a polydimethylsiloxane (PDMS)-based microfluidic system, constructed on a silicon wafer with a 2.0 microm electrically insulating layer of silicon dioxide, is demonstrated. This microfluidic system consists of a 2.0 cm open microchannel fabricated on a PDMS slab, which can reversibly adhere to the silicon wafer to form a hybrid microfluidic device. Aside from mechanically serving as a robust bottom substrate to seal the channel and support the microfluidic system, the silicon wafer is exploited to achieve field-effect flow control by grounding the semiconductive silicon medium. When an electric field is applied through the channel, a radial electric potential gradient is created across the silicon dioxide layer that allows for direct control of the zeta potential and the resulting electroosmotic flow (EOF). By configuring this microfluidic system with two power supplies at both ends of the microchannel, the applied electric potentials can be varied for manipulating the polarity and the magnitude of the radial electric potential gradient across the silicon dioxide layer. At the same time, the longitudinal potential gradient through the microchannel, which is used to induce EOF, is held constant. The results of EOF control in this hybrid microfluidic system are presented for phosphate buffer at pH 3 and pH 5. It is also demonstrated that EOF control can be performed at higher solution pH of 6 and 7.4 by modifying the silicon wafer surface with cetyltrimethylammonium bromide (CTAB) prior to assembly of the hybrid microfluidic system. Results of EOF control from this study are compared with those reported in the literature involving the use of other microfluidic devices under comparable solution conditions.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

J S Buch, P C Wang, D L DeVoe, C S Lee. 2001. Field-effect flow control in a polydimethylsiloxane-based microfluidic system.. https://doi.org/10.1002/1522-2683(200110)22%3A18%3C3902%3A%3Aaid-elps3902%3E3.0.co%3B2-k

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

KEEP EXPLORING

Related citations

An electrochemical investigation of ligand-binding abilities of film-entrapped myoglobin.

Film-entrapped myoglobin exhibits well-defined electrochemistry which, upon ligand binding, displays a titratable redox potential shift. This effect has been observed to be highly dependent on the charged state of involved films. We have demonstrated that this approach may act as a model system for studies of molecular recognition between proteins and ligands.

Cetrimonium↗

Specific analyte-electrolyte additive interaction in transient isotachophoresis-capillary electrophoresis.

While cationic surfactants are usually included in the separation electrolyte to reverse the electroosmotic flow, the presence of the surfactant may also offer a means of capillary electrophoresis (CE) separation selectivity control over the anionic analytes, especially those that are prone to ion-pairing interaction. For one such analyte anion, iodide, the formation of several ion-association/partition products with cetyltrimethylammonium chloride (CTAC) was first discovered when optimizing (decelerating) iodide mobility (in order to achieve effective transient isotachophoretic stacking). At comparatively high concentrations of iodide (> or = 0.01 mM) and the cationic surfactant well above the critical micelle concentration (25 mM), an additional peak due to interactions with the CTAC micelle was recorded, with a UV absorption spectrum fairly different from those of both interacting partners and also the iodide-monomeric surfactant ion pair. Never observed before in normal CE mode, this phenomenon is believed to have occurred due to the enrichment effect of the initial isotachophoresis state.

Cetrimonium↗

Trace ion analysis of seawater by capillary electrophoresis: determination of iodide using transient isotachophoretic preconcentration.

An improved transient isotachophoresis (tITP) procedure for the preconcentration of iodide from highly saline matrices was developed with the objective to quantify iodide in seawater by capillary electrophoresis (CE). The procedure takes advantage of introducing cetyltrimethylammonium chloride into the high-sodium chloride background electrolyte, which due to a specific interaction with iodide amended placement of the analyte at a large distance from the matrix chloride (the latter performed the role of a leading anion). Computer simulation showed that 2-(N-morpholino)ethanesulfonate could be adopted as a suitable terminating ion to enable isotachophoretic focusing at the beginning of the CE run. Under optimized tITP conditions, the sensitivity response of iodide was improved by a factor of 140 over normal CE mode. This allowed for direct UV detection of as low as 0.6 microg/L iodide and made feasible CE analysis of undiluted surface seawater samples where iodide was found at a 30 microg/L level. The applicability of the proposed tITP-CE method could apparently be extended to the determination of other trace seawater anions (e.g., iodate).

Cetrimonium↗