The University of Southampton
University of Southampton Institutional Repository

Hyperpolarised [2-13C]-pyruvate by 13C SABRE in an acetone/water mixture

Hyperpolarised [2-13C]-pyruvate by 13C SABRE in an acetone/water mixture
Hyperpolarised [2-13C]-pyruvate by 13C SABRE in an acetone/water mixture
Signal Amplification By Reversible Exchange (SABRE) can provide strong signal enhancement (SE) to an array of molecules through reversible exchange of parahydrogen (pH2) derived hydrides and a suitable substrate coordinated to a transition metal. Among the substrates that can be used as a probe for hyperpolarised NMR and MRI, pyruvate has gained much attention. SABRE can hyperpolarise pyruvate in a low cost, fast, and reversible fashion that does not involve technologically demanding equipment. Most SABRE polarization studies have been done using methanol-d4 as a solvent, which is not suitable for in vivo application. The main goal of this work was to obtain hyperpolarized pyruvate in a solvent other than methanol which may open the door to further purification steps and enable a method to polarize pyruvate in water in future. This work demonstrates hyperpolarization of the [2-13C]pyruvate as well as [1-13C]pyruvate by SABRE in an acetone/water solvent system at room temperature as an alternative to methanol, which is commonly used. NMR signals are detected using a 1.1 T benchtop NMR spectrometer. In this work we have primarily focused on the study of [2-13C]pyruvate and investigated the effect of catalyst concentration, DMSO presence and water vs. acetone solvent concentration on the signal enhancement. The relaxation times for [2-13C]-pyruvate solutions are reported in the hope of informing the development of future purification methods.
5668-5674
Bondar, Oksana A.
7e0517b6-7826-4966-86bf-6cb493c709b5
Moustafa, Gamal A.I.
1a452cdc-4856-4243-9864-b391fb115f07
Robertson, Thomas B.R.
957b392c-1212-4721-bd6d-d1e00ed50a09
Bondar, Oksana A.
7e0517b6-7826-4966-86bf-6cb493c709b5
Moustafa, Gamal A.I.
1a452cdc-4856-4243-9864-b391fb115f07
Robertson, Thomas B.R.
957b392c-1212-4721-bd6d-d1e00ed50a09

Bondar, Oksana A., Moustafa, Gamal A.I. and Robertson, Thomas B.R. (2024) Hyperpolarised [2-13C]-pyruvate by 13C SABRE in an acetone/water mixture. Analyst, 149 (23), 5668-5674. (doi:10.1039/D4AN01005A).

Record type: Article

Abstract

Signal Amplification By Reversible Exchange (SABRE) can provide strong signal enhancement (SE) to an array of molecules through reversible exchange of parahydrogen (pH2) derived hydrides and a suitable substrate coordinated to a transition metal. Among the substrates that can be used as a probe for hyperpolarised NMR and MRI, pyruvate has gained much attention. SABRE can hyperpolarise pyruvate in a low cost, fast, and reversible fashion that does not involve technologically demanding equipment. Most SABRE polarization studies have been done using methanol-d4 as a solvent, which is not suitable for in vivo application. The main goal of this work was to obtain hyperpolarized pyruvate in a solvent other than methanol which may open the door to further purification steps and enable a method to polarize pyruvate in water in future. This work demonstrates hyperpolarization of the [2-13C]pyruvate as well as [1-13C]pyruvate by SABRE in an acetone/water solvent system at room temperature as an alternative to methanol, which is commonly used. NMR signals are detected using a 1.1 T benchtop NMR spectrometer. In this work we have primarily focused on the study of [2-13C]pyruvate and investigated the effect of catalyst concentration, DMSO presence and water vs. acetone solvent concentration on the signal enhancement. The relaxation times for [2-13C]-pyruvate solutions are reported in the hope of informing the development of future purification methods.

Text
d4an01005a - Version of Record
Available under License Creative Commons Attribution.
Download (1MB)

More information

Accepted/In Press date: 8 October 2024
Published date: 21 October 2024

Identifiers

Local EPrints ID: 495764
URI: http://eprints.soton.ac.uk/id/eprint/495764
PURE UUID: dd39052c-21ab-41d1-afd9-c8b3f6713ee6
ORCID for Oksana A. Bondar: ORCID iD orcid.org/0000-0003-0686-1509
ORCID for Gamal A.I. Moustafa: ORCID iD orcid.org/0000-0002-9940-0033
ORCID for Thomas B.R. Robertson: ORCID iD orcid.org/0000-0001-9394-6185

Catalogue record

Date deposited: 21 Nov 2024 17:53
Last modified: 22 Nov 2024 03:05

Export record

Altmetrics

Contributors

Author: Oksana A. Bondar ORCID iD

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×