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Difference between revisions of "Urzi 2023 Anal Chem"

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{{Publication
{{Publication
|title=Urzì C, Meyer C, Nuoffer JM, Vermathen P (2023) Methods for oxygen determination in an NMR bioreactor as a surrogate marker for metabolomic studies in living cell cultures. https://doi.org/10.1021/acs.analchem.3c02314
|title=Urzì C, Meyer C, Nuoffer JM, Vermathen P (2023) Methods for oxygen determination in an NMR bioreactor as a surrogate marker for metabolomic studies in living cell cultures. https://doi.org/10.1021/acs.analchem.3c02314
|info=Anal Chem [Epub ahead of print]. [https://www.ncbi.nlm.nih.gov/pubmed/37989262 PMID: 37989262 Open Access]
|info=Anal Chem 95:17486-93. [https://www.ncbi.nlm.nih.gov/pubmed/37989262 PMID: 37989262 Open Access]
|authors=Urzi Christian, Meyer Christoph, Nuoffer Jean-Marc, Vermathen Peter
|authors=Urzi Christian, Meyer Christoph, Nuoffer Jean-Marc, Vermathen Peter
|year=2023
|year=2023

Latest revision as of 15:39, 19 December 2023

Publications in the MiPMap
Urzì C, Meyer C, Nuoffer JM, Vermathen P (2023) Methods for oxygen determination in an NMR bioreactor as a surrogate marker for metabolomic studies in living cell cultures. https://doi.org/10.1021/acs.analchem.3c02314

» Anal Chem 95:17486-93. PMID: 37989262 Open Access

Urzi Christian, Meyer Christoph, Nuoffer Jean-Marc, Vermathen Peter (2023) Anal Chem

Abstract: Nuclear magnetic resonance (NMR) approaches have been described as a powerful method for measuring oxygen in tissue cultures and body fluids by using relaxation time dependencies of substances on pO2. The present NMR study describes methods to longitudinally monitor global, in situ intracellular, and spatially resolved oxygen tension in culture media and 3D cell cultures using relaxation times of water without the need to use external sensors. 1H NMR measurements of water using a modified inversion recovery pulse scheme were employed for global, i.e., intra- and extracellular oxygen estimation in an NMR-bioreactor. The combination of 1H relaxation time T1 and diffusion measurements of water was employed for in situ cellular oxygen content determination. Spatially selective water relaxation time estimations were used for spatially resolved oxygen quantification along the NMR tube length. The inclusion in a study protocol of the presented techniques for oxygen quantification, as a surrogate marker of oxidative phosphorylation (OXPHOS), provides the possibility to measure mitochondrial respiration and metabolic changes simultaneously.

Bioblast editor: Plangger M O2k-Network Lab: CH Bern Nuoffer JM


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2023-11