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Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice

Compound 2,3-dimethyl-4H-furo[3,2-c]coumarin is a coumarin derivative that could be labeled with (125)I. The process of labeling was started using 1 mg of the compound, 50 µg CAT oxidizing agent, 30 min as reaction time at pH with a yield about 95%. The (125)I-coumarin derivative was stable for abou...

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Detalles Bibliográficos
Autores principales: Abd Elhalim, S.M., Ibrahim, I.T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pergamon Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259903/
https://www.ncbi.nlm.nih.gov/pubmed/25464192
http://dx.doi.org/10.1016/j.apradiso.2014.09.011
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author Abd Elhalim, S.M.
Ibrahim, I.T.
author_facet Abd Elhalim, S.M.
Ibrahim, I.T.
author_sort Abd Elhalim, S.M.
collection PubMed
description Compound 2,3-dimethyl-4H-furo[3,2-c]coumarin is a coumarin derivative that could be labeled with (125)I. The process of labeling was started using 1 mg of the compound, 50 µg CAT oxidizing agent, 30 min as reaction time at pH with a yield about 95%. The (125)I-coumarin derivative was stable for about 48 h. Radiochemical purity of the labeled compound was performed by electrophoresis and HPLC. The labeled compound was separated with purity about 95%. Tumor transplantation to produce a solid tumor in the right leg of albino mice was made by intramuscular injection of 2×10(6) EAC (Ehrlish acittes carcinoma cells). Biodistribution study of (125)I-coumarin derivative revealed that the uptake in tumor bearing leg was over 5% at 1 h and 4 h post-injection. This uptake encourages the use of (123)I-coumarin derivative in imaging of tumor sites.
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spelling pubmed-42599032015-01-01 Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice Abd Elhalim, S.M. Ibrahim, I.T. Appl Radiat Isot Article Compound 2,3-dimethyl-4H-furo[3,2-c]coumarin is a coumarin derivative that could be labeled with (125)I. The process of labeling was started using 1 mg of the compound, 50 µg CAT oxidizing agent, 30 min as reaction time at pH with a yield about 95%. The (125)I-coumarin derivative was stable for about 48 h. Radiochemical purity of the labeled compound was performed by electrophoresis and HPLC. The labeled compound was separated with purity about 95%. Tumor transplantation to produce a solid tumor in the right leg of albino mice was made by intramuscular injection of 2×10(6) EAC (Ehrlish acittes carcinoma cells). Biodistribution study of (125)I-coumarin derivative revealed that the uptake in tumor bearing leg was over 5% at 1 h and 4 h post-injection. This uptake encourages the use of (123)I-coumarin derivative in imaging of tumor sites. Pergamon Press 2015-01 /pmc/articles/PMC4259903/ /pubmed/25464192 http://dx.doi.org/10.1016/j.apradiso.2014.09.011 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Abd Elhalim, S.M.
Ibrahim, I.T.
Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title_full Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title_fullStr Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title_full_unstemmed Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title_short Radioiodination of 2,3-dimethyl-4H-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
title_sort radioiodination of 2,3-dimethyl-4h-furo[3,2-c]coumarin and biological evaluation in solid tumor bearing mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4259903/
https://www.ncbi.nlm.nih.gov/pubmed/25464192
http://dx.doi.org/10.1016/j.apradiso.2014.09.011
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