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Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats
C4 (cobalt dichloride-N-acetylcysteine [1% CoCl(2):2% NAC]) is a novel magnetic resonance imaging contrast marker that facilitates visualization of implanted radioactive seeds in cancer brachytherapy. We evaluated the toxicity of C4. Rats were assigned to control (0% CoCl(2):NAC), low-dose (0.1% CoC...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304599/ https://www.ncbi.nlm.nih.gov/pubmed/30631353 http://dx.doi.org/10.1155/2018/9173452 |
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author | Wang, Li Gagea, Mihai Martirosyan, Karen Johansen, Mary Madden, Timothy Norberg, Lisa Culotta, Kirk S. Frank, Steven J. |
author_facet | Wang, Li Gagea, Mihai Martirosyan, Karen Johansen, Mary Madden, Timothy Norberg, Lisa Culotta, Kirk S. Frank, Steven J. |
author_sort | Wang, Li |
collection | PubMed |
description | C4 (cobalt dichloride-N-acetylcysteine [1% CoCl(2):2% NAC]) is a novel magnetic resonance imaging contrast marker that facilitates visualization of implanted radioactive seeds in cancer brachytherapy. We evaluated the toxicity of C4. Rats were assigned to control (0% CoCl(2):NAC), low-dose (0.1% CoCl(2):2% NAC), reference-dose (C4), and high-dose (10% CoCl(2):2% NAC) groups. Agent was injected into the left quadriceps femoris muscle of the rats. Endpoints were organ and body weights, hematology, and serum chemistry and histopathologic changes of tissues at 48 hours and 28 and 63 days after dosing. Student's t tests were used. No abnormalities in clinical signs, terminal body and organ weights, or hematologic and serum chemistry were noted, and no gross or histopathologic lesions of systemic tissue toxicity were found in any treatment group at any time point studied. At the site of injection, concentration-dependent acute responses were observed in all treatment groups at 48 hours after dosing and were recovered by 28 days. No myofiber degeneration or necrosis was observed at 28 or 63 days in any group. In conclusion, a single intramuscular dose of C4 produced no acute or chronic systemic toxicity or inflammation in rats, suggesting that C4 may be toxicologically safe for clinical use in cancer brachytherapy. |
format | Online Article Text |
id | pubmed-6304599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-63045992019-01-10 Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats Wang, Li Gagea, Mihai Martirosyan, Karen Johansen, Mary Madden, Timothy Norberg, Lisa Culotta, Kirk S. Frank, Steven J. J Toxicol Research Article C4 (cobalt dichloride-N-acetylcysteine [1% CoCl(2):2% NAC]) is a novel magnetic resonance imaging contrast marker that facilitates visualization of implanted radioactive seeds in cancer brachytherapy. We evaluated the toxicity of C4. Rats were assigned to control (0% CoCl(2):NAC), low-dose (0.1% CoCl(2):2% NAC), reference-dose (C4), and high-dose (10% CoCl(2):2% NAC) groups. Agent was injected into the left quadriceps femoris muscle of the rats. Endpoints were organ and body weights, hematology, and serum chemistry and histopathologic changes of tissues at 48 hours and 28 and 63 days after dosing. Student's t tests were used. No abnormalities in clinical signs, terminal body and organ weights, or hematologic and serum chemistry were noted, and no gross or histopathologic lesions of systemic tissue toxicity were found in any treatment group at any time point studied. At the site of injection, concentration-dependent acute responses were observed in all treatment groups at 48 hours after dosing and were recovered by 28 days. No myofiber degeneration or necrosis was observed at 28 or 63 days in any group. In conclusion, a single intramuscular dose of C4 produced no acute or chronic systemic toxicity or inflammation in rats, suggesting that C4 may be toxicologically safe for clinical use in cancer brachytherapy. Hindawi 2018-12-02 /pmc/articles/PMC6304599/ /pubmed/30631353 http://dx.doi.org/10.1155/2018/9173452 Text en Copyright © 2018 Li Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Wang, Li Gagea, Mihai Martirosyan, Karen Johansen, Mary Madden, Timothy Norberg, Lisa Culotta, Kirk S. Frank, Steven J. Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title | Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title_full | Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title_fullStr | Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title_full_unstemmed | Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title_short | Toxicity Evaluation of a Novel Magnetic Resonance Imaging Marker, CoCl2-N-Acetylcysteine, in Rats |
title_sort | toxicity evaluation of a novel magnetic resonance imaging marker, cocl2-n-acetylcysteine, in rats |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304599/ https://www.ncbi.nlm.nih.gov/pubmed/30631353 http://dx.doi.org/10.1155/2018/9173452 |
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