Targeted Desorption Electrospray Ionization Mass Spectrometry Imaging for Drug Distribution, Toxicity, and Tissue Classification Studies.
Andreas DannhornMaria Luisa DoriaJames McKenziePaolo IngleseJohn G SwalesGregory HammNicole StrittmatterGareth MaglennonSadaf Ghaem-MaghamiRichard J A GoodwinZoltan TakatsPublished in: Metabolites (2023)
With increased use of mass spectrometry imaging (MSI) in support of pharmaceutical research and development, there are opportunities to develop analytical pipelines that incorporate exploratory high-performance analysis with higher capacity and faster targeted MSI. Therefore, to enable faster MSI data acquisition we present analyte-targeted desorption electrospray ionization-mass spectrometry imaging (DESI-MSI) utilizing a triple-quadrupole (TQ) mass analyzer. The evaluated platform configuration provided superior sensitivity compared to a conventional time-of-flight (TOF) mass analyzer and thus holds the potential to generate data applicable to pharmaceutical research and development. The platform was successfully operated with sampling rates up to 10 scans/s, comparing positively to the 1 scan/s commonly used on comparable DESI-TOF setups. The higher scan rate enabled investigation of the desorption/ionization processes of endogenous lipid species such as phosphatidylcholines and a co-administered cassette of four orally dosed drugs-erlotininb, moxifloxacin, olanzapine, and terfenadine. This was used to enable understanding of the impact of the desorption/ionization processes in order to optimize the operational parameters, resulting in improved compound coverage for olanzapine and the main olanzapine metabolite, hydroxy-olanzapine, in brain tissue sections compared to DESI-TOF analysis or matrix-assisted laser desorption/ionization (MALDI) platforms. The approach allowed reducing the amount of recorded information, thus reducing the size of datasets from up to 150 GB per experiment down to several hundred MB. The improved performance was demonstrated in case studies investigating the suitability of this approach for mapping drug distribution, spatially resolved profiling of drug-induced nephrotoxicity, and molecular-histological tissue classification of ovarian tumors specimens.
Keyphrases
- mass spectrometry
- high resolution
- drug induced
- liquid chromatography
- gas chromatography
- liver injury
- high performance liquid chromatography
- capillary electrophoresis
- computed tomography
- tandem mass spectrometry
- machine learning
- deep learning
- cancer therapy
- electronic health record
- chemotherapy induced
- big data
- high throughput
- healthcare
- emergency department
- multiple sclerosis
- risk assessment
- magnetic resonance imaging
- high density
- dual energy
- climate change
- magnetic resonance