Mechanochemical Synthesis of New Praziquantel Cocrystals: Solid-State Characterization and Solubility

• Published in: Crystal growth & design Vol. 24; no. 11; pp. 4668 - 4681
• Main Authors: Mureşan-Pop, Marieta, Simon, Simion, Bodoki, Ede, Simon, Viorica, Turza, Alexandru, Todea, Milica, Vulpoi, Adriana, Magyari, Klara, Iacob, Bogdan C., Bărăian, Alexandra Iulia, Gołdyn, Mateusz, Gomes, Clara S. B., Susana, Margarida, Duarte, M. Teresa, André, Vânia
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 05-06-2024
• ISSN: 1528-7483; 1528-7505
• DOI: 10.1021/acs.cgd.4c00296

New cocrystals of praziquantel with suberic, 3-hydroxybenzoic, benzene-1,2,4,5-tetracarboxylic, trimesic, and 5-hydroxyisophthalic acids were obtained through ball milling experiments. The optimal conditions for the milling process were chosen by changing the solvent volume and the mechanical action time. Supramolecular interactions in the new cocrystals are detailed based on single-crystal X-ray diffraction analysis, confirming the expected formation of hydrogen bonds between the praziquantel carbonyl group and the carboxyl (or hydroxyl) moieties of the coformers. Different structural characterization techniques were performed for all samples, but the praziquantel:suberic acid cocrystal includes a wider range of investigations such as thermal analysis, infrared and X-ray photoelectron spectroscopies, and SEM microscopy. The stability for up to five months was established by keeping it under extreme conditions of temperature and humidity. Solubility studies were carried out for all the new forms disclosed herein and compared with the promising cocrystals previously reported with salicylic, 4-aminosalicylic, vanillic, and oxalic acids. HPLC analyses revealed a higher solubility for most of the new cocrystal forms, as compared to pure praziquantel.