Microfluidic devices fabricated from polymers exhibit great potential in bi
ological analyses. Poly(dimethylsiloxane) (PDMS) has shown promise as a sub
strate for rapid prototyping of devices. Despite this, disagreement exists
in the literature as to the ability of PDMS to support electroosmotic (EO)
flow and the stability of that flow over time. We demonstrate that in low i
onic strength solutions near neutral in pH, oxidized PDMS had a four-fold g
reater EO mobility (mu (eo)) compared to native PDMS. The greater mu (eo) w
as maintained irrespective of whether glass or PDMS was used as a support f
orming one side of the channel, This enhanced mu (eo) was preserved as long
as the channels were filled with an aqueous solution. Upon exposure of the
channels to air, the mobility decreased by a factor of two with a half-lif
e of 9 h. The EO properties of the air-exposed, oxidized PDMS were regenera
ted by exposure to strong base. High ionic strength, neutral in pH buffers
compatible with living eukaryotic cells diminished the EO flow in the oxidi
zed PDMS devices to a much greater extent than in the native PDMS devices.
For analyses utilizing intact and living cells, oxidation of PDMS may not b
e an effective strategy to substantially increase the mu (eo). (C) 2001 Els
evier Science B.V. All rights reserved.