High‐throughput liquid chromatography/mass spectrometry method for the quantitation of small molecules using accurate mass technologies in supporting discovery drug screening. (26th December 2012)
- Record Type:
- Journal Article
- Title:
- High‐throughput liquid chromatography/mass spectrometry method for the quantitation of small molecules using accurate mass technologies in supporting discovery drug screening. (26th December 2012)
- Main Title:
- High‐throughput liquid chromatography/mass spectrometry method for the quantitation of small molecules using accurate mass technologies in supporting discovery drug screening
- Authors:
- Ding, Xiao
Ghobarah, Hesham
Zhang, Xiaolin
Jaochico, Allan
Liu, Xingrong
Deshmukh, Gauri
Liederer, Bianca M.
Hop, Cornelis E. C. A.
Dean, Brian - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm6461-sec-0001" sec-type="section"> <title>RATIONALE</title> <p>Drug discovery samples are routinely analyzed using liquid chromatography/tandem mass spectrometry <bold>(</bold>LC/MS/MS) methods on triple quadrupole mass spectrometers employing multiple reaction monitoring (MRM). In order to improve analysis throughput, quantitation of small molecules on a quadrupole time‐of‐flight (QqTOF) instrument using TOF scan and high‐resolution MRM (MRM‐HR) modes was evaluated in this study.</p> </sec> <sec id="rcm6461-sec-0002" sec-type="section"> <title>METHODS</title> <p>Cassette dosed plasma and brain samples from nine compounds were extracted using a protein precipitation method. Separation was achieved by reversed‐phase liquid chromatography. Mass spectrometric analysis was performed using TOF scan and high‐resolution MRM approaches on a QqTOF mass spectrometer with turbo‐ionspray ionization. Results were compared to those obtained on a triple quadrupole mass spectrometer.</p> </sec> <sec id="rcm6461-sec-0003" sec-type="section"> <title>RESULTS</title> <p>The dynamic range varied depending on compounds and instruments and was similar between the MRM on QqQ and full TOF scan mode on QqTOF. Linear or quadratic regression and 1/x<sup>2</sup> weighting were used. Resolution on the QqTOF instrument was around 32000 and mass accuracy was within 4.4 ppm. The MRM‐HR method showed better<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="rcm6461-sec-0001" sec-type="section"> <title>RATIONALE</title> <p>Drug discovery samples are routinely analyzed using liquid chromatography/tandem mass spectrometry <bold>(</bold>LC/MS/MS) methods on triple quadrupole mass spectrometers employing multiple reaction monitoring (MRM). In order to improve analysis throughput, quantitation of small molecules on a quadrupole time‐of‐flight (QqTOF) instrument using TOF scan and high‐resolution MRM (MRM‐HR) modes was evaluated in this study.</p> </sec> <sec id="rcm6461-sec-0002" sec-type="section"> <title>METHODS</title> <p>Cassette dosed plasma and brain samples from nine compounds were extracted using a protein precipitation method. Separation was achieved by reversed‐phase liquid chromatography. Mass spectrometric analysis was performed using TOF scan and high‐resolution MRM approaches on a QqTOF mass spectrometer with turbo‐ionspray ionization. Results were compared to those obtained on a triple quadrupole mass spectrometer.</p> </sec> <sec id="rcm6461-sec-0003" sec-type="section"> <title>RESULTS</title> <p>The dynamic range varied depending on compounds and instruments and was similar between the MRM on QqQ and full TOF scan mode on QqTOF. Linear or quadratic regression and 1/x<sup>2</sup> weighting were used. Resolution on the QqTOF instrument was around 32000 and mass accuracy was within 4.4 ppm. The MRM‐HR method showed better sensitivity compared to the TOF scan method, and was comparable to the MRM on a QqQ mass spectrometer. Assay accuracy was within ±25%.</p> </sec> <sec id="rcm6461-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>A TOF scan method allowed the use of the generic method without compound‐specific optimization and was an alternative choice for routine high‐throughput quantitation of small molecules. The MRM‐HR method on the QqTOF showed good sensitivity which was comparable to that obtained by the MRM method on the triple quadrupole mass spectrometer. Copyright © 2012 John Wiley &amp; Sons, Ltd.</p> </sec> </abstract> … (more)
- Is Part Of:
- Rapid communications in mass spectrometry. Volume 27:Number 3(2013)
- Journal:
- Rapid communications in mass spectrometry
- Issue:
- Volume 27:Number 3(2013)
- Issue Display:
- Volume 27, Issue 3 (2013)
- Year:
- 2013
- Volume:
- 27
- Issue:
- 3
- Issue Sort Value:
- 2013-0027-0003-0000
- Page Start:
- 401
- Page End:
- 408
- Publication Date:
- 2012-12-26
- Subjects:
- Mass spectrometry -- Periodicals
543.65 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/rcm.6461 ↗
- 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:
- 3932.xml