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Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid

Tafamidis, chemical formula C(14)H(7)Cl(2)NO(3), is a drug used to delay disease progression in adults suffering from transthyretin amyloidosis, and is marketed worldwide under different tradenames as a free acid or in the form of its meglumine salt. The free acid (CAS no. 594839-88-0) is reported t...

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Autores principales: Masciocchi, Norberto, Abbinante, Vincenzo Mirco, Zambra, Marco, Barreca, Giuseppe, Zampieri, Massimo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656987/
https://www.ncbi.nlm.nih.gov/pubmed/36364244
http://dx.doi.org/10.3390/molecules27217411
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author Masciocchi, Norberto
Abbinante, Vincenzo Mirco
Zambra, Marco
Barreca, Giuseppe
Zampieri, Massimo
author_facet Masciocchi, Norberto
Abbinante, Vincenzo Mirco
Zambra, Marco
Barreca, Giuseppe
Zampieri, Massimo
author_sort Masciocchi, Norberto
collection PubMed
description Tafamidis, chemical formula C(14)H(7)Cl(2)NO(3), is a drug used to delay disease progression in adults suffering from transthyretin amyloidosis, and is marketed worldwide under different tradenames as a free acid or in the form of its meglumine salt. The free acid (CAS no. 594839-88-0) is reported to crystallize as distinct (polymorphic) crystal forms, the thermal stability and structural features of which remained thus far undisclosed. In this paper, we present—by selectively isolating highly pure batches of Tafamidis Form 1 and Tafamidis Form 4—the full characterization of these solids, in terms of crystal structures (determined using state-of-the-art structural powder diffraction methods) and spectroscopic and thermal properties. Beyond conventional thermogravimetric and calorimetric analyses, variable-temperature X-ray diffraction was employed to measure the highly anisotropic response of these (poly)crystalline materials to thermal stimuli and enabled the determination of the linear and volumetric thermal expansion coefficients and of the related indicatrix. Both crystal phases are monoclinic and contain substantially flat and π-π stacked Tafamidis molecules, arranged as centrosymmetric dimers by strong O-H···O bonds; weaker C-H···N contacts give rise, in both polymorphs, to infinite ribbons, which guarantee the substantial stiffness of the crystals in the direction of their elongation. Complete knowledge of the structural models will foster the usage of full-pattern quantitative phase analyses of Tafamidis in drug and polymorphic mixtures, an important aspect in both the forensic and the industrial sectors.
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spelling pubmed-96569872022-11-15 Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid Masciocchi, Norberto Abbinante, Vincenzo Mirco Zambra, Marco Barreca, Giuseppe Zampieri, Massimo Molecules Article Tafamidis, chemical formula C(14)H(7)Cl(2)NO(3), is a drug used to delay disease progression in adults suffering from transthyretin amyloidosis, and is marketed worldwide under different tradenames as a free acid or in the form of its meglumine salt. The free acid (CAS no. 594839-88-0) is reported to crystallize as distinct (polymorphic) crystal forms, the thermal stability and structural features of which remained thus far undisclosed. In this paper, we present—by selectively isolating highly pure batches of Tafamidis Form 1 and Tafamidis Form 4—the full characterization of these solids, in terms of crystal structures (determined using state-of-the-art structural powder diffraction methods) and spectroscopic and thermal properties. Beyond conventional thermogravimetric and calorimetric analyses, variable-temperature X-ray diffraction was employed to measure the highly anisotropic response of these (poly)crystalline materials to thermal stimuli and enabled the determination of the linear and volumetric thermal expansion coefficients and of the related indicatrix. Both crystal phases are monoclinic and contain substantially flat and π-π stacked Tafamidis molecules, arranged as centrosymmetric dimers by strong O-H···O bonds; weaker C-H···N contacts give rise, in both polymorphs, to infinite ribbons, which guarantee the substantial stiffness of the crystals in the direction of their elongation. Complete knowledge of the structural models will foster the usage of full-pattern quantitative phase analyses of Tafamidis in drug and polymorphic mixtures, an important aspect in both the forensic and the industrial sectors. MDPI 2022-11-01 /pmc/articles/PMC9656987/ /pubmed/36364244 http://dx.doi.org/10.3390/molecules27217411 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Masciocchi, Norberto
Abbinante, Vincenzo Mirco
Zambra, Marco
Barreca, Giuseppe
Zampieri, Massimo
Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title_full Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title_fullStr Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title_full_unstemmed Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title_short Thermal and Structural Characterization of Two Crystalline Polymorphs of Tafamidis Free Acid
title_sort thermal and structural characterization of two crystalline polymorphs of tafamidis free acid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656987/
https://www.ncbi.nlm.nih.gov/pubmed/36364244
http://dx.doi.org/10.3390/molecules27217411
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