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Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH
Acidosis is a useful biomarker for tumor diagnoses and for evaluating early response to anti-cancer treatments. Despite these useful applications, there are few methods for non-invasively measuring tumor extracellular pH, and none are routinely used in clinics. Responsive MRI contrast agents have be...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870419/ https://www.ncbi.nlm.nih.gov/pubmed/35200394 http://dx.doi.org/10.3390/bios12020134 |
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author | Pollard, Alyssa C. de la Cerda, Jorge Schuler, F. William Pollard, Tyler R. Kotrotsou, Aikaterini Pisaneschi, Federica Pagel, Mark D. |
author_facet | Pollard, Alyssa C. de la Cerda, Jorge Schuler, F. William Pollard, Tyler R. Kotrotsou, Aikaterini Pisaneschi, Federica Pagel, Mark D. |
author_sort | Pollard, Alyssa C. |
collection | PubMed |
description | Acidosis is a useful biomarker for tumor diagnoses and for evaluating early response to anti-cancer treatments. Despite these useful applications, there are few methods for non-invasively measuring tumor extracellular pH, and none are routinely used in clinics. Responsive MRI contrast agents have been developed, and they undergo a change in MRI signal with pH. However, these signal changes are concentration-dependent, and it is difficult to accurately measure the concentration of an MRI contrast agent in vivo. PET/MRI provides a unique opportunity to overcome this concentration dependence issue by using the PET component to report on the concentration of the pH-responsive MRI agent. Herein, we synthesized PET/MRI co-agents based on the design of a pH-dependent MRI agent, and we have correlated pH with the r(1) relaxivity of the MRI co-agent. We have also developed a procedure that uses PET radioactivity measurements and MRI R(1) relaxation rate measurements to determine the r(1) relaxivity of the MRI co-agent, which can then be used to estimate pH. This simultaneous PET/MRI procedure accurately measured pH in solution, with a precision that depended on the concentration of the MRI co-agent. We used our procedure to measure extracellular pH in a subcutaneous flank model of MIA PaCa-2 pancreatic cancer. Although the PET co-agents were stable in serum, post-imaging studies showed evidence that the PET co-agents were degraded in vivo. These results showed that tumor acidosis can be evaluated with simultaneous PET/MRI, although improvements are needed to more precisely measure MRI R(1) relaxation rates, and ensure the in vivo stability of the agents. |
format | Online Article Text |
id | pubmed-8870419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88704192022-02-25 Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH Pollard, Alyssa C. de la Cerda, Jorge Schuler, F. William Pollard, Tyler R. Kotrotsou, Aikaterini Pisaneschi, Federica Pagel, Mark D. Biosensors (Basel) Article Acidosis is a useful biomarker for tumor diagnoses and for evaluating early response to anti-cancer treatments. Despite these useful applications, there are few methods for non-invasively measuring tumor extracellular pH, and none are routinely used in clinics. Responsive MRI contrast agents have been developed, and they undergo a change in MRI signal with pH. However, these signal changes are concentration-dependent, and it is difficult to accurately measure the concentration of an MRI contrast agent in vivo. PET/MRI provides a unique opportunity to overcome this concentration dependence issue by using the PET component to report on the concentration of the pH-responsive MRI agent. Herein, we synthesized PET/MRI co-agents based on the design of a pH-dependent MRI agent, and we have correlated pH with the r(1) relaxivity of the MRI co-agent. We have also developed a procedure that uses PET radioactivity measurements and MRI R(1) relaxation rate measurements to determine the r(1) relaxivity of the MRI co-agent, which can then be used to estimate pH. This simultaneous PET/MRI procedure accurately measured pH in solution, with a precision that depended on the concentration of the MRI co-agent. We used our procedure to measure extracellular pH in a subcutaneous flank model of MIA PaCa-2 pancreatic cancer. Although the PET co-agents were stable in serum, post-imaging studies showed evidence that the PET co-agents were degraded in vivo. These results showed that tumor acidosis can be evaluated with simultaneous PET/MRI, although improvements are needed to more precisely measure MRI R(1) relaxation rates, and ensure the in vivo stability of the agents. MDPI 2022-02-20 /pmc/articles/PMC8870419/ /pubmed/35200394 http://dx.doi.org/10.3390/bios12020134 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pollard, Alyssa C. de la Cerda, Jorge Schuler, F. William Pollard, Tyler R. Kotrotsou, Aikaterini Pisaneschi, Federica Pagel, Mark D. Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title | Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title_full | Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title_fullStr | Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title_full_unstemmed | Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title_short | Radiometal-Based PET/MRI Contrast Agents for Sensing Tumor Extracellular pH |
title_sort | radiometal-based pet/mri contrast agents for sensing tumor extracellular ph |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870419/ https://www.ncbi.nlm.nih.gov/pubmed/35200394 http://dx.doi.org/10.3390/bios12020134 |
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