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Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study

Production of a biocompatible hyperpolarized bolus for signal amplification by reversible exchange (SABRE) could open the door to simple clinical diagnosis via magnetic resonance imaging. Essential to successful progression to preclinical/clinical applications is the determination of the toxicology...

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Detalles Bibliográficos
Autores principales: Manoharan, Anand, Rayner, Peter J., Iali, Wissam, Burns, Michael J., Perry, V. Hugh, Duckett, Simon B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838797/
https://www.ncbi.nlm.nih.gov/pubmed/29232489
http://dx.doi.org/10.1002/cmdc.201700725
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author Manoharan, Anand
Rayner, Peter J.
Iali, Wissam
Burns, Michael J.
Perry, V. Hugh
Duckett, Simon B.
author_facet Manoharan, Anand
Rayner, Peter J.
Iali, Wissam
Burns, Michael J.
Perry, V. Hugh
Duckett, Simon B.
author_sort Manoharan, Anand
collection PubMed
description Production of a biocompatible hyperpolarized bolus for signal amplification by reversible exchange (SABRE) could open the door to simple clinical diagnosis via magnetic resonance imaging. Essential to successful progression to preclinical/clinical applications is the determination of the toxicology profile of the SABRE reaction mixture. Herein, we exemplify the cytotoxicity of the SABRE approach using in vitro cell assays. We conclude that the main cause of the observed toxicity is due to the SABRE catalyst. We therefore illustrate two catalyst removal methods: one involving deactivation and ion‐exchange chromatography, and the second using biphasic catalysis. These routes produce a bolus suitable for future in vivo study.
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spelling pubmed-58387972018-03-12 Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study Manoharan, Anand Rayner, Peter J. Iali, Wissam Burns, Michael J. Perry, V. Hugh Duckett, Simon B. ChemMedChem Full Papers Production of a biocompatible hyperpolarized bolus for signal amplification by reversible exchange (SABRE) could open the door to simple clinical diagnosis via magnetic resonance imaging. Essential to successful progression to preclinical/clinical applications is the determination of the toxicology profile of the SABRE reaction mixture. Herein, we exemplify the cytotoxicity of the SABRE approach using in vitro cell assays. We conclude that the main cause of the observed toxicity is due to the SABRE catalyst. We therefore illustrate two catalyst removal methods: one involving deactivation and ion‐exchange chromatography, and the second using biphasic catalysis. These routes produce a bolus suitable for future in vivo study. John Wiley and Sons Inc. 2018-01-18 2018-02-20 /pmc/articles/PMC5838797/ /pubmed/29232489 http://dx.doi.org/10.1002/cmdc.201700725 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Manoharan, Anand
Rayner, Peter J.
Iali, Wissam
Burns, Michael J.
Perry, V. Hugh
Duckett, Simon B.
Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title_full Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title_fullStr Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title_full_unstemmed Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title_short Achieving Biocompatible SABRE: An in vitro Cytotoxicity Study
title_sort achieving biocompatible sabre: an in vitro cytotoxicity study
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5838797/
https://www.ncbi.nlm.nih.gov/pubmed/29232489
http://dx.doi.org/10.1002/cmdc.201700725
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