Buscarini Alessandra, Zaworotko Michael J, Matos Catiúcia R M O, Grepioni Fabrizia, Contini Laura, Capsoni Doretta, Friuli Valeria, Maggi Lauretta, Bruni Giovanna
Department of Chemistry, Physical Chemistry Section & C.S.G.I. (Consorzio Interuniversitario per lo Sviluppo dei Sistemi a Grande Interfase), University of Pavia, Via Taramelli 16, 27100 Pavia, Italy.
Department of Chemical Sciences and Bernal Institute, University of Limerick, V94 T9PX Limerick, Ireland.
Molecules. 2024 Nov 27;29(23):5610. doi: 10.3390/molecules29235610.
Pimozide is a first-generation antipsychotic used in the treatment of schizophrenia, Gilles de la Tourette syndrome, and other chronic psychoses. Its in vivo efficacy is limited by poor solubility and consequent poor bioavailability. Therefore, adipic acid was used as a coformer for the preparation of a binary product with improved pharmaceutical properties. The thermal behavior of the liquid-assisted grinding products of compositions included in the range 0.1 < < 0.9 has been interpreted using a thermo-dynamic model according to which the two components originate a new crystalline entity in molar ratio pimozide:adipic acid 0.66:0.33, which forms an eutectic system with adipic acid. The model was confirmed using the quantitative analysis of the melting peaks and using the X-ray diffraction measurements from powders and single crystals. In particular, the latter have demonstrated that the new entity resulting from the pimozide:adipic acid 0.66:0.33 composition is actually salt . The crystalline product was characterized, from a pharmaceutical perspective, in terms of solubility and wettability (contact angle). Then, a tablet formulation was developed, and its dissolution behavior was compared to a commercial product considered as a reference. The new entity showed improved pharmaceutical properties in terms of solubility and wettability compared to the pure drug in both deionized water and bio-relevant fluids simulating oral administration in fed and fasted conditions. The tablets containing the new crystalline form can make this virtually insoluble drug available for absorption within minutes regardless of the variability in gastric conditions.
匹莫齐特是一种第一代抗精神病药物,用于治疗精神分裂症、图雷特综合征及其他慢性精神病。其体内疗效受溶解度差及由此导致的生物利用度低的限制。因此,己二酸被用作共形成剂来制备具有改善药物性质的二元产品。已使用热力学模型解释了组成范围为0.1< <0.9的液体辅助研磨产品的热行为,根据该模型,两种组分以匹莫齐特:己二酸摩尔比0.66:0.33形成一种新的结晶实体,该实体与己二酸形成低共熔体系。通过对熔融峰的定量分析以及对粉末和单晶的X射线衍射测量对该模型进行了验证。特别是,后者表明由匹莫齐特:己二酸0.66:0.33组成产生的新实体实际上是盐。从药物角度对结晶产品的溶解度和润湿性(接触角)进行了表征。然后,开发了一种片剂配方,并将其溶出行为与作为参考的市售产品进行了比较。与去离子水中的纯药物以及模拟进食和禁食条件下口服给药的生物相关流体中的纯药物相比,新实体在溶解度和润湿性方面均表现出改善的药物性质。含有新晶型的片剂可使这种几乎不溶的药物在数分钟内即可被吸收,而不受胃部条件变化的影响。