A miniature condensed‐phase membrane introduction mass spectrometry (CP‐MIMS) probe for direct and on‐line measurements of pharmaceuticals and contaminants in small, complex samples. (30th April 2013)
- Record Type:
- Journal Article
- Title:
- A miniature condensed‐phase membrane introduction mass spectrometry (CP‐MIMS) probe for direct and on‐line measurements of pharmaceuticals and contaminants in small, complex samples. (30th April 2013)
- Main Title:
- A miniature condensed‐phase membrane introduction mass spectrometry (CP‐MIMS) probe for direct and on‐line measurements of pharmaceuticals and contaminants in small, complex samples
- Authors:
- Duncan, Kyle D.
Willis, Megan D.
Krogh, Erik T.
Gill, Christopher G. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm6560-sec-0001" sec-type="section"> <title>RATIONALE</title> <p>High‐throughput, automated analytical measurements are desirable in many analytical scenarios, as are rapid sample pre‐screening techniques to identify 'positive' samples for subsequent measurements using more time‐consuming conventional methodologies (e.g., liquid chromatography/mass spectrometry (LC/MS)). A miniature condensed‐phase membrane introduction mass spectrometry (CP‐MIMS) probe for the direct and continuous, on‐line measurement of pharmaceuticals and environmental contaminants in small, complex samples is presented.</p> </sec> <sec id="rcm6560-sec-0002" sec-type="section"> <title>METHODS</title> <p>A miniature polydimethylsiloxane hollow fibre membrane (PDMS‐HFM) probe is coupled with an electrospray ionization (ESI) triple quadrupole mass spectrometer. Analytes are transported from the probe to the ESI source by a methanol acceptor phase. The probe can be autosampler mounted and directly inserted in small samples (≥400 μL) allowing continuous and simultaneous pptr–ppb level detection of target analytes (chlorophenols, triclosan, gemfibrozil, nonylphenol) in complex samples (artificial urine, beer, natural water, waste water, plant tissue).</p> </sec> <sec id="rcm6560-sec-0003" sec-type="section"> <title>RESULTS</title> <p>The probe has been characterized and optimized for acceptor phase flow rate, sample<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm6560-sec-0001" sec-type="section"> <title>RATIONALE</title> <p>High‐throughput, automated analytical measurements are desirable in many analytical scenarios, as are rapid sample pre‐screening techniques to identify 'positive' samples for subsequent measurements using more time‐consuming conventional methodologies (e.g., liquid chromatography/mass spectrometry (LC/MS)). A miniature condensed‐phase membrane introduction mass spectrometry (CP‐MIMS) probe for the direct and continuous, on‐line measurement of pharmaceuticals and environmental contaminants in small, complex samples is presented.</p> </sec> <sec id="rcm6560-sec-0002" sec-type="section"> <title>METHODS</title> <p>A miniature polydimethylsiloxane hollow fibre membrane (PDMS‐HFM) probe is coupled with an electrospray ionization (ESI) triple quadrupole mass spectrometer. Analytes are transported from the probe to the ESI source by a methanol acceptor phase. The probe can be autosampler mounted and directly inserted in small samples (≥400 μL) allowing continuous and simultaneous pptr–ppb level detection of target analytes (chlorophenols, triclosan, gemfibrozil, nonylphenol) in complex samples (artificial urine, beer, natural water, waste water, plant tissue).</p> </sec> <sec id="rcm6560-sec-0003" sec-type="section"> <title>RESULTS</title> <p>The probe has been characterized and optimized for acceptor phase flow rate, sample mixing and probe washing. Signal response times, detection limits and calibration data are given for selected ion monitoring (SIM) and tandem mass spectrometry (MS/MS) measurements of target analytes at trace levels. Comparisons with flow cell type CP‐MIMS systems are given. Analyte depletion effects are evaluated for small samples (≥400 μL). On‐line measurements in small volumes of complex samples, temporally resolved reaction monitoring and <italic>in situ/in vivo</italic> demonstrations are presented.</p> </sec> <sec id="rcm6560-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>The miniature CP‐MIMS probe developed was successfully used for the direct, on‐line detection of target analytes in small volumes (40 mL to 400 μL) of complex samples at pptr to low ppb levels. The probe can be readily automated as well as deployed for <italic>in situ/in vivo</italic> monitoring, including reaction monitoring, small sample measurements and direct insertion in living plant tissue. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </sec> </abstract> … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 27:Number 11(2013)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 27:Number 11(2013)
- Issue Display:
- Volume 27, Issue 11 (2013)
- Year:
- 2013
- Volume:
- 27
- Issue:
- 11
- Issue Sort Value:
- 2013-0027-0011-0000
- Page Start:
- 1213
- Page End:
- 1221
- Publication Date:
- 2013-04-30
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.6560 ↗
- Languages:
- English
- ISSNs:
- 0951-4198
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 7254.440000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3171.xml