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Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies

We report thermal, X-ray diffraction (XRD) and cytotoxicity studies of complexes of fluconazole (FCZ) with Cu (II), Fe(II), Cd(II), Co(II), Ni(II), and Mn(II). From XRD measurements, FCZ and its metal complexes were identified as polycrystalline. Marked differences in the X-ray patterns of drug and...

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Autores principales: Ali, Syed Imran, Lei, Zi-Ning, Ali, Mohsin, Kojima, Konatsu, Ahmed, Mansoor, Peng, Richard, Yang, Dong-Hua, Haider, Syed Moazzam, Ayatollahi, Seyed Abdulmajid, Chen, Zhe-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757997/
https://www.ncbi.nlm.nih.gov/pubmed/33680020
http://dx.doi.org/10.22037/ijpr.2020.1101142
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author Ali, Syed Imran
Lei, Zi-Ning
Ali, Mohsin
Kojima, Konatsu
Ahmed, Mansoor
Peng, Richard
Yang, Dong-Hua
Haider, Syed Moazzam
Ayatollahi, Seyed Abdulmajid
Chen, Zhe-Sheng
author_facet Ali, Syed Imran
Lei, Zi-Ning
Ali, Mohsin
Kojima, Konatsu
Ahmed, Mansoor
Peng, Richard
Yang, Dong-Hua
Haider, Syed Moazzam
Ayatollahi, Seyed Abdulmajid
Chen, Zhe-Sheng
author_sort Ali, Syed Imran
collection PubMed
description We report thermal, X-ray diffraction (XRD) and cytotoxicity studies of complexes of fluconazole (FCZ) with Cu (II), Fe(II), Cd(II), Co(II), Ni(II), and Mn(II). From XRD measurements, FCZ and its metal complexes were identified as polycrystalline. Marked differences in the X-ray patterns of drug and its metal complexes revealed that the complexes are indeed different compounds and not just the mixture of the starting materials. Unlike pristine FCZ, which did not exhibit cytotoxicity, three complexes derived from Fe(II), Cu(II) and Co (II) proved to be effective in the cytotoxicity assay. The Cu(II)-FCZ exhibited significant activity against SNB-19, HCT-15, COLO-205, and KB-3-1 cell lines, while Fe(II)-FCZ and Co(II)-FCZ were found cytotoxic only to KB-3-1 cell line. For the pure FCZ, thermogravimetry revealed massive weight loss in the temperature range of 215 to 297 °C, due to the volatilization of FCZ. All the complexes followed multi-stage degradation profiles, eventually resulting in the formation of metal oxides. For pure FCZ, differential scanning calorimetry revealed melting point at 137 °C, followed by two further endothermic transitions at 294 °C and 498.44 °C representing the volatilization and subsequent degradation of FCZ, respectively. The absence of endothermic FCZ melting peak at around 137 °C indicates that the complexes represent different compounds. All complexes exhibit endothermic transitions at around 240-300 °C, representing melting and removal of ligand moiety, followed by another endothermic transition at around 498-499 °C, representing the ligand decomposition.
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spelling pubmed-77579972021-03-05 Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies Ali, Syed Imran Lei, Zi-Ning Ali, Mohsin Kojima, Konatsu Ahmed, Mansoor Peng, Richard Yang, Dong-Hua Haider, Syed Moazzam Ayatollahi, Seyed Abdulmajid Chen, Zhe-Sheng Iran J Pharm Res Original Article We report thermal, X-ray diffraction (XRD) and cytotoxicity studies of complexes of fluconazole (FCZ) with Cu (II), Fe(II), Cd(II), Co(II), Ni(II), and Mn(II). From XRD measurements, FCZ and its metal complexes were identified as polycrystalline. Marked differences in the X-ray patterns of drug and its metal complexes revealed that the complexes are indeed different compounds and not just the mixture of the starting materials. Unlike pristine FCZ, which did not exhibit cytotoxicity, three complexes derived from Fe(II), Cu(II) and Co (II) proved to be effective in the cytotoxicity assay. The Cu(II)-FCZ exhibited significant activity against SNB-19, HCT-15, COLO-205, and KB-3-1 cell lines, while Fe(II)-FCZ and Co(II)-FCZ were found cytotoxic only to KB-3-1 cell line. For the pure FCZ, thermogravimetry revealed massive weight loss in the temperature range of 215 to 297 °C, due to the volatilization of FCZ. All the complexes followed multi-stage degradation profiles, eventually resulting in the formation of metal oxides. For pure FCZ, differential scanning calorimetry revealed melting point at 137 °C, followed by two further endothermic transitions at 294 °C and 498.44 °C representing the volatilization and subsequent degradation of FCZ, respectively. The absence of endothermic FCZ melting peak at around 137 °C indicates that the complexes represent different compounds. All complexes exhibit endothermic transitions at around 240-300 °C, representing melting and removal of ligand moiety, followed by another endothermic transition at around 498-499 °C, representing the ligand decomposition. Shaheed Beheshti University of Medical Sciences 2020 /pmc/articles/PMC7757997/ /pubmed/33680020 http://dx.doi.org/10.22037/ijpr.2020.1101142 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ali, Syed Imran
Lei, Zi-Ning
Ali, Mohsin
Kojima, Konatsu
Ahmed, Mansoor
Peng, Richard
Yang, Dong-Hua
Haider, Syed Moazzam
Ayatollahi, Seyed Abdulmajid
Chen, Zhe-Sheng
Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title_full Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title_fullStr Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title_full_unstemmed Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title_short Metal (II) Complexes of Fluconazole: Thermal, XRD and Cytotoxicity Studies
title_sort metal (ii) complexes of fluconazole: thermal, xrd and cytotoxicity studies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7757997/
https://www.ncbi.nlm.nih.gov/pubmed/33680020
http://dx.doi.org/10.22037/ijpr.2020.1101142
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