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New Pharmaceutical Salts of Trazodone
New pharmaceutically acceptable salts of trazodone (trazodone hydrogen bromide and trazodone 1-hydroxy-2-naphthonic acid) for the treatment of central nervous system disorders are synthesized and described. Although trazodone salts are poorly crystalline, single-crystal X-ray diffraction data for tr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867375/ https://www.ncbi.nlm.nih.gov/pubmed/33540851 http://dx.doi.org/10.3390/molecules26030769 |
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author | Jaśkowska, Jolanta Zaręba, Przemysław Drabczyk, Anna Kozak, Agnieszka Madura, Izabela D. Majka, Zbigniew Pindelska, Edyta |
author_facet | Jaśkowska, Jolanta Zaręba, Przemysław Drabczyk, Anna Kozak, Agnieszka Madura, Izabela D. Majka, Zbigniew Pindelska, Edyta |
author_sort | Jaśkowska, Jolanta |
collection | PubMed |
description | New pharmaceutically acceptable salts of trazodone (trazodone hydrogen bromide and trazodone 1-hydroxy-2-naphthonic acid) for the treatment of central nervous system disorders are synthesized and described. Although trazodone salts are poorly crystalline, single-crystal X-ray diffraction data for trazodone 1-hydroxy-2-naphthonic acid were collected and analyzed as well as compared to the previously described crystal structure of commercially available trazodone hydrochloride. The powder samples of all new salts were characterized by Fourier transform infrared spectroscopy, X-ray diffraction and (13)C solid-state nuclear magnetic resonance spectroscopy. Spectroscopic studies were supported by gauge including projector augmented wave (GIPAW) calculations of carbon chemical shielding constants. The main goal of our research was to find salts with better physicochemical properties and to make an attempt to associate them with both the anion structure and the most prominent interactions exhibited by the protonated trazodone cation. The dissolution profiles of trazodone from tablets prepared from various salts with lactose monohydrate were investigated. The studies revealed that salts with simple anions show a fast release of the drug while the presence of more complex anion, more strongly interacting with the cation, effects a slow-release profile of the active substance and can be used for the preparation of the tables with a delay or prolonged mode of action. |
format | Online Article Text |
id | pubmed-7867375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78673752021-02-07 New Pharmaceutical Salts of Trazodone Jaśkowska, Jolanta Zaręba, Przemysław Drabczyk, Anna Kozak, Agnieszka Madura, Izabela D. Majka, Zbigniew Pindelska, Edyta Molecules Article New pharmaceutically acceptable salts of trazodone (trazodone hydrogen bromide and trazodone 1-hydroxy-2-naphthonic acid) for the treatment of central nervous system disorders are synthesized and described. Although trazodone salts are poorly crystalline, single-crystal X-ray diffraction data for trazodone 1-hydroxy-2-naphthonic acid were collected and analyzed as well as compared to the previously described crystal structure of commercially available trazodone hydrochloride. The powder samples of all new salts were characterized by Fourier transform infrared spectroscopy, X-ray diffraction and (13)C solid-state nuclear magnetic resonance spectroscopy. Spectroscopic studies were supported by gauge including projector augmented wave (GIPAW) calculations of carbon chemical shielding constants. The main goal of our research was to find salts with better physicochemical properties and to make an attempt to associate them with both the anion structure and the most prominent interactions exhibited by the protonated trazodone cation. The dissolution profiles of trazodone from tablets prepared from various salts with lactose monohydrate were investigated. The studies revealed that salts with simple anions show a fast release of the drug while the presence of more complex anion, more strongly interacting with the cation, effects a slow-release profile of the active substance and can be used for the preparation of the tables with a delay or prolonged mode of action. MDPI 2021-02-02 /pmc/articles/PMC7867375/ /pubmed/33540851 http://dx.doi.org/10.3390/molecules26030769 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jaśkowska, Jolanta Zaręba, Przemysław Drabczyk, Anna Kozak, Agnieszka Madura, Izabela D. Majka, Zbigniew Pindelska, Edyta New Pharmaceutical Salts of Trazodone |
title | New Pharmaceutical Salts of Trazodone |
title_full | New Pharmaceutical Salts of Trazodone |
title_fullStr | New Pharmaceutical Salts of Trazodone |
title_full_unstemmed | New Pharmaceutical Salts of Trazodone |
title_short | New Pharmaceutical Salts of Trazodone |
title_sort | new pharmaceutical salts of trazodone |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867375/ https://www.ncbi.nlm.nih.gov/pubmed/33540851 http://dx.doi.org/10.3390/molecules26030769 |
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