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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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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. |
format | Online Article Text |
id | pubmed-7774281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yamadayuji dimerizationofdoxorubicincausesitsprecipitation |