Mechanochemical synthesis, characterization, and thermal behavior of meloxicam cocrystals with salicylic acid, fumaric acid, and malic acid

• Autor(a) principal: Fernandes, Richard Perosa [UNESP]
• Data de Publicação: 2019
• Outros Autores: do Nascimento, André Luiz Carneiro Soares [UNESP], Carvalho, Ana Carina Sobral [UNESP], Teixeira, José Augusto [UNESP], Ionashiro, Massao [UNESP], Caires, Flávio Junior [UNESP]
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://dx.doi.org/10.1007/s10973-019-08118-7; http://hdl.handle.net/11449/190181
• topic: Cocrystal; Fumaric acid; Malic acid; Meloxicam; Salicylic acid; Thermal analysis

A liquid-assisted grinding approach was used to synthesize three cocrystals between the coformers: salicylic acid, fumaric acid, and malic acid with meloxicam, a nonsteroidal anti-inflammatory drug. The spectroscopic techniques, Raman and Fourier transform infrared (FTIR), confirm the formation of these compounds by showing evidence of hydrogen bonds between NH or OH and CO groups. Powder X-ray diffraction verified the formation of the cocrystals by comparing the results with a crystallographic database. Differential scanning calorimetry (DSC), simultaneous thermogravimetry and differential scanning calorimetry (TG-DSC), evolved gas analysis (EGA by TG-FTIR), DSC-photovisual analysis, and videos of the cocrystals being heated were used to study the thermal behavior, analyze the composition, identify polymorphic transitions in meloxicam cocrystal with malic acid, and understand the decomposition phenomena of these solids. The malic acid compound shows a unique degradation step that was confirmed by TG-DSC data and FTIR analysis of the residue formed. A solubility test was performed: fumaric cocrystal showed an enhanced performance compared to pure drug, and malic and salicylic cocrystals showed a slower dissolution profile.