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Development of an ambient ionisation mass spectrometry method for metabolomic analysis of blood microsamples

Orlowsky, Andrea (2021) Development of an ambient ionisation mass spectrometry method for metabolomic analysis of blood microsamples. Other thesis, Murdoch University.

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Abstract

Atmospheric Solids Analysis Probe mass spectrometry (ASAP-MS) has applications in food science, pharmaceuticals and toxicology but has not been applied to global metabolic profiling of biofluids. Coupled with dried blood microsampling techniques, ASAP-MS may provide rapid blood sample analyses benefitting medical and forensic sciences. This study aimed to develop a methodology utilising ASAP-MS for the metabolomic analyses of blood samples and comparison of venipuncture (serum and plasma) and capillary dried blood microsamples (DBM) using dried blood spot (DBS) and volumetric absorptive microsampling (VAM) matrices.

Method development and optimisation on the Waters RADIAN-ASAP® assessed desolvation gas temperature, cone voltage, and corona current. The optimised parameters were applied to caffeine and lipid standards to determine the reproducibility of the instrument. The sample extraction methods (solvent, dilution, storage vial) and sampling regime for introducing samples into the ion source (sample volume, cooling mechanisms between acquisition) were assessed. The optimised methods were applied to venipuncture and capillary microsamples, and results were compared to ultra-high performance liquid chromatography-mass spectrometry {UPLC-MS). The coefficient of variation {CV) and principal component analysis (PCA) was used to assess analytical reproducibility.

ASAP-MS parameters of 600 °C gas temperature, cone voltage of 15 V and corona current of 4 µA generate optimal signal intensity. Methanol extractions of caffeine in polypropylene microcentrifuge tubes produced the most reproducible data {CV = 4.7%), compared to extractions with acetonitrile {CV = 13.5%), isopropyl alcohol {CV = 15.2%) or methanol extractions in glass {CV= 8.1%). A methanol quench-bath to cool the glass sampler between acquisitions shortened the analytical run time while improving reproducibility {CV = 2.3%). UP LC-MS analysis of the lipid compound mixture detected 52 lipid species, of which ASAP-MS reproducibly detected 47 across both polarities. ASAP-MS detected fewer molecular features with a CV<30% (n = 583 positive, n = 571 negative) than UPLC-MS (n = 937 positive, n = 1392 negative) when analysing venipuncture and capillary DBM. ASAP-MS detects more molecular features, with higher CV%, in capillary DBM than venipuncture samples. A simplified field extraction technique yields results equivalent to laboratory-based extractions for DBM. While early experimental results are promising, further evaluations should focus on reducing the variability in QC samples through appropriate data pre-processing pipelines, and the inclusion of an internal standard for data normalisation.

Item Type: Thesis (Other)
Murdoch Affiliation(s): Medical, Molecular and Forensic Sciences
Notes: This is an accelerated Research Masters with Training (aRMT) thesis
Supervisor(s): Tobe, Shane, Loo, Ruey Leng and Speers, James
URI: http://researchrepository.murdoch.edu.au/id/eprint/63786
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