Screening of coformers for quercetin cocrystals through mechanochemical methods

Quercetin (QUE) is a nutraceutical compound that exhibits pharmacological properties such as antioxidant, cardioprotective, anti-ulcer, and anti-inflammatory effects. Although QUE is well-known for its benefits, its efficacy is limited due to low solubility. Thus, cocrystallization acts as an intere...

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Detalhes bibliográficos
Autores: De Souza, Fayene Zeferino Ribeiro [UNESP], De Almeida, Amanda Cosmo [UNESP], Ferreira, Patrícia Osorio [UNESP], Fernandes, Richard Perosa [UNESP], Caires, Flávio Junior [UNESP]
Formato: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:Brasil
Recursos:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/223320
Acesso em linha:http://dx.doi.org/10.26850/1678-4618eqj.v47.1.2022.p64-75
http://hdl.handle.net/11449/223320
Access Level:acceso abierto
Palavra-chave:Cocrystallization
Flavonoid
Mechanochemistry
Nutraceutical
Thermal analysis
Descrição
Resumo:Quercetin (QUE) is a nutraceutical compound that exhibits pharmacological properties such as antioxidant, cardioprotective, anti-ulcer, and anti-inflammatory effects. Although QUE is well-known for its benefits, its efficacy is limited due to low solubility. Thus, cocrystallization acts as an interesting approach to improve the solubility - among other properties - of this compound. In this work, cocrystallization screening was applied through neat grinding (NG) and liquid-assisted grinding (LAG), in which QUE and four cocrystal formers (benzamide, picolinamide, isonicotinamide, and pyrazinoic acid) were tested. The precursors and QUE-coformer systems were characterized using thermoanalytical techniques (TG-DTA), X-ray powder diffraction (XRPD), and Fourier transform infrared (FTIR) spectroscopy. The results showed the formation of QUE cocrystals with picolinamide and isonicotinamide coformers in a 1:1 stoichiometric ratio. Furthermore, although coformers are isomers, spectroscopic and thermal data suggest that the supramolecular synthons involved in cocrystallization are different.