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Development of an optimised method for the analysis of human blood plasma samples by atmospheric solids analysis probe mass spectrometry

Abstract:
Analysis of small-molecule metabolites in plasma has the potential for development as a clinical diagnostic and prognostic tool. Atmospheric solids analysis probe mass spectrometry (ASAP-MS) is capable of performing rapid metabolite and small molecule fingerprinting, and has the potential for use in a clinical setting. Combining ASAP-MS data with a predictive model could provide clinicians with a rapid patient risk metric, anticipating disease progression and response to treatment, and thereby aiding in treatment decisions. In order to develop predictive models, experimental errors and uncertainties must be minimised, requiring a robust experimental protocol. In the present study we have performed ASAP-MS measurements on plasma samples from patients recruited for two prospective clinical studies: the Oxford Acute Myocardial Infarction (OxAMI) study; and the Oxford Abdominal Aortic Aneurysm (OxAAA) study. Through a carefully designed series of measurements, we have optimised the method of sample introduction, together with a number of key instrument and data acquisition parameters. Following the optimisation process, we are consistently able to record high quality mass spectra for plasma samples. Typical coefficients of variation for individual mass peaks are in the range from 20%–50%, overlapping with those obtained using more sophisticated LC-MS approaches. The measurement protocol optimises mass spectral quality and reproducibility, while retaining the simplicity of measurement required for use in a clinical setting. While the protocol was developed using plasma samples from two specific patient cohorts, the method can be generalised to any plasma measurements.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1016/j.ijms.2024.117386

Authors

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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0002-8815-6768
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0002-1942-3666
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0009-0008-2532-8199
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0001-8132-6130


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
218514/Z/19/Z


Publisher:
Elsevier
Journal:
International Journal of Mass Spectrometry More from this journal
Volume:
508
Article number:
117386
Publication date:
2024-12-10
Acceptance date:
2024-12-04
DOI:
EISSN:
1873-2798
ISSN:
1387-3806


Language:
English
Keywords:
Pubs id:
1635863
UUID:
uuid_640824bc-6c99-4fdb-b81a-627d25cd22a3
Local pid:
pubs:1635863
Source identifiers:
W4389668265
Deposit date:
2025-12-08
ARK identifier:

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