Web Release Date: October 18,
Chemically Etched Open Tubular and Monolithic Emitters for Nanoelectrospray Ionization Mass Spectrometry
Biological Sciences Division, Pacific Northwest National Laboratory, P.O. Box 999, Richland, Washington 99352
Received for review June 22, 2006. Accepted September 12, 2006.
Abstract:
We have developed a new procedure for fabricating fused-silica emitters for electrospray ionization-mass spectrometry (ESI-MS) in which the end of a bare fused-silica
capillary is immersed into aqueous hydrofluoric acid, and
water is pumped through the capillary to prevent etching
of the interior. Surface tension causes the etchant to climb
the capillary exterior, and the etch rate in the resulting
meniscus decreases as a function of distance from the
bulk solution. Etching continues until the silica touching
the hydrofluoric acid reservoir is completely removed,
essentially stopping the etch process. The resulting emitters have no internal taper, making them much less prone
to clogging compared to, e.g., pulled emitters. The high
aspect ratios and extremely thin walls at the orifice
facilitate very low flow rate operation; stable ESI-MS
signals were obtained for model analytes from 5-
m-diameter emitters at a flow rate of 5 nL/min with a high
degree of interemitter reproducibility. In extensive evaluation, the etched emitters were found to enable approximately four times as many LC-MS analyses of
proteomic samples before failing compared with conventional pulled emitters. The fabrication procedure was also
employed to taper the ends of polymer monolith-containing silica capillaries for use as ESI emitters. In contrast
to previous work, the monolithic material protrudes
beyond the fused-silica capillaries, improving the monolith-assisted electrospray process.
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