Cargando…

Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate

Cerium oxide nanoparticles (CONPs) have a unique surface redox chemistry that appears to selectively protect normal tissues from radiation induced damage. Our prior research exploring the biocompatibility of polymer-coated CONPs found further study of poly-acrylic acid (PAA)-coated CONPs was warrant...

Descripción completa

Detalles Bibliográficos
Autores principales: McDonagh, Philip Reed, Gobalakrishnan, Sundaresan, Rabender, Christopher, Vijayaragavan, Vimalan, Zweit, Jamal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457862/
https://www.ncbi.nlm.nih.gov/pubmed/37631358
http://dx.doi.org/10.3390/pharmaceutics15082144
_version_ 1785097026381283328
author McDonagh, Philip Reed
Gobalakrishnan, Sundaresan
Rabender, Christopher
Vijayaragavan, Vimalan
Zweit, Jamal
author_facet McDonagh, Philip Reed
Gobalakrishnan, Sundaresan
Rabender, Christopher
Vijayaragavan, Vimalan
Zweit, Jamal
author_sort McDonagh, Philip Reed
collection PubMed
description Cerium oxide nanoparticles (CONPs) have a unique surface redox chemistry that appears to selectively protect normal tissues from radiation induced damage. Our prior research exploring the biocompatibility of polymer-coated CONPs found further study of poly-acrylic acid (PAA)-coated CONPs was warranted due to improved systemic biodistribution and rapid renal clearance. This work further explores PAA-CONPs’ radioprotective efficacy and mechanism of action related to tumor microenvironment pH. An ex vivo TUNEL assay was used to measure PAA-CONPs’ protection of the irradiated mouse colon in comparison to the established radioprotector amifostine. [(18)F]FDG PET imaging of spontaneous colon tumors was utilized to determine the effects of PAA-CONPs on tumor radiation response. In vivo MRI and an ex vivo clonogenic assay were used to determine pH effects on PAA-CONPs’ radioprotection in irradiated tumor-bearing mice. PAA-CONPs showed excellent radioprotective efficacy in the normal colon that was equivalent to uncoated CONPs and amifostine. [(18)F]FDG PET imaging showed PAA-CONPs do not affect tumor response to radiation. Normalization of tumor pH allowed some radioprotection of tumors by PAA-CONPs, which may explain their lack of tumor radioprotection in the acidic tumor microenvironment. Overall, PAA-CONPs meet the criteria for clinical application as a radioprotective therapeutic agent and are an excellent candidate for further study.
format Online
Article
Text
id pubmed-10457862
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-104578622023-08-27 Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate McDonagh, Philip Reed Gobalakrishnan, Sundaresan Rabender, Christopher Vijayaragavan, Vimalan Zweit, Jamal Pharmaceutics Article Cerium oxide nanoparticles (CONPs) have a unique surface redox chemistry that appears to selectively protect normal tissues from radiation induced damage. Our prior research exploring the biocompatibility of polymer-coated CONPs found further study of poly-acrylic acid (PAA)-coated CONPs was warranted due to improved systemic biodistribution and rapid renal clearance. This work further explores PAA-CONPs’ radioprotective efficacy and mechanism of action related to tumor microenvironment pH. An ex vivo TUNEL assay was used to measure PAA-CONPs’ protection of the irradiated mouse colon in comparison to the established radioprotector amifostine. [(18)F]FDG PET imaging of spontaneous colon tumors was utilized to determine the effects of PAA-CONPs on tumor radiation response. In vivo MRI and an ex vivo clonogenic assay were used to determine pH effects on PAA-CONPs’ radioprotection in irradiated tumor-bearing mice. PAA-CONPs showed excellent radioprotective efficacy in the normal colon that was equivalent to uncoated CONPs and amifostine. [(18)F]FDG PET imaging showed PAA-CONPs do not affect tumor response to radiation. Normalization of tumor pH allowed some radioprotection of tumors by PAA-CONPs, which may explain their lack of tumor radioprotection in the acidic tumor microenvironment. Overall, PAA-CONPs meet the criteria for clinical application as a radioprotective therapeutic agent and are an excellent candidate for further study. MDPI 2023-08-15 /pmc/articles/PMC10457862/ /pubmed/37631358 http://dx.doi.org/10.3390/pharmaceutics15082144 Text en © 2023 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
McDonagh, Philip Reed
Gobalakrishnan, Sundaresan
Rabender, Christopher
Vijayaragavan, Vimalan
Zweit, Jamal
Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title_full Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title_fullStr Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title_full_unstemmed Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title_short Molecular Imaging Investigations of Polymer-Coated Cerium Oxide Nanoparticles as a Radioprotective Therapeutic Candidate
title_sort molecular imaging investigations of polymer-coated cerium oxide nanoparticles as a radioprotective therapeutic candidate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457862/
https://www.ncbi.nlm.nih.gov/pubmed/37631358
http://dx.doi.org/10.3390/pharmaceutics15082144
work_keys_str_mv AT mcdonaghphilipreed molecularimaginginvestigationsofpolymercoatedceriumoxidenanoparticlesasaradioprotectivetherapeuticcandidate
AT gobalakrishnansundaresan molecularimaginginvestigationsofpolymercoatedceriumoxidenanoparticlesasaradioprotectivetherapeuticcandidate
AT rabenderchristopher molecularimaginginvestigationsofpolymercoatedceriumoxidenanoparticlesasaradioprotectivetherapeuticcandidate
AT vijayaragavanvimalan molecularimaginginvestigationsofpolymercoatedceriumoxidenanoparticlesasaradioprotectivetherapeuticcandidate
AT zweitjamal molecularimaginginvestigationsofpolymercoatedceriumoxidenanoparticlesasaradioprotectivetherapeuticcandidate