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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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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. |
format | Online Article Text |
id | pubmed-5838797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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