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Dimerization of Doxorubicin Causes Its Precipitation

[Image: see text] Doxorubicin (DOX) is commonly used in chemotherapy and biomedical research because of its potent anticancer activity. Although DOX is water soluble, it precipitates when interacting with buffers, such as phosphate-buffered saline, or with drugs such as 5-fluorouracil (5-FU) and hep...

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Autor principal: Yamada, Yuji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774281/
https://www.ncbi.nlm.nih.gov/pubmed/33403285
http://dx.doi.org/10.1021/acsomega.0c04925
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author Yamada, Yuji
author_facet Yamada, Yuji
author_sort Yamada, Yuji
collection PubMed
description [Image: see text] Doxorubicin (DOX) is commonly used in chemotherapy and biomedical research because of its potent anticancer activity. Although DOX is water soluble, it precipitates when interacting with buffers, such as phosphate-buffered saline, or with drugs such as 5-fluorouracil (5-FU) and heparin. This study reports that DOX precipitates in neutral buffers and 5-FU solution because of the formation of covalently bonded DOX dimers. Additionally, this study proposes a structure for the DOX dimer and a mechanism for dimerization on the basis of mass spectrometry in combination with an experiment to establish the reaction model. The DOX dimer/precipitate formation might be an important phenomenon, considering the frequent use of DOX in chemotherapy and biomedical research.
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spelling pubmed-77742812021-01-04 Dimerization of Doxorubicin Causes Its Precipitation Yamada, Yuji ACS Omega [Image: see text] Doxorubicin (DOX) is commonly used in chemotherapy and biomedical research because of its potent anticancer activity. Although DOX is water soluble, it precipitates when interacting with buffers, such as phosphate-buffered saline, or with drugs such as 5-fluorouracil (5-FU) and heparin. This study reports that DOX precipitates in neutral buffers and 5-FU solution because of the formation of covalently bonded DOX dimers. Additionally, this study proposes a structure for the DOX dimer and a mechanism for dimerization on the basis of mass spectrometry in combination with an experiment to establish the reaction model. The DOX dimer/precipitate formation might be an important phenomenon, considering the frequent use of DOX in chemotherapy and biomedical research. American Chemical Society 2020-12-15 /pmc/articles/PMC7774281/ /pubmed/33403285 http://dx.doi.org/10.1021/acsomega.0c04925 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Yamada, Yuji
Dimerization of Doxorubicin Causes Its Precipitation
title Dimerization of Doxorubicin Causes Its Precipitation
title_full Dimerization of Doxorubicin Causes Its Precipitation
title_fullStr Dimerization of Doxorubicin Causes Its Precipitation
title_full_unstemmed Dimerization of Doxorubicin Causes Its Precipitation
title_short Dimerization of Doxorubicin Causes Its Precipitation
title_sort dimerization of doxorubicin causes its precipitation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774281/
https://www.ncbi.nlm.nih.gov/pubmed/33403285
http://dx.doi.org/10.1021/acsomega.0c04925
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