Olivera Camila, Boscolo Oriana, Dobrecky Cecilia, Ortega Claudia A, Favier Laura S, Cianchino Valeria A, Flor Sabrina, Lucangioli Silvia
Departamento de Tecnología Farmacéutica, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junin 956, Buenos Aires C1113AAD, Argentina.
Instituto de Tecnología Farmacéutica y Biofarmacia (InTecFyB), Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Junin 956, Buenos Aires C1113AAD, Argentina.
Pharmaceutics. 2024 Dec 24;17(1):5. doi: 10.3390/pharmaceutics17010005.
Trihexyphenidyl (THP) has been widely used for over three decades as pediatric pharmacotherapy in patients affected by segmental and generalized dystonia. In order to achieve effective and safe pharmacotherapy for this population, new formulations are needed. The aim of this work is the development of trihexyphenidyl orodispersible minitablets (ODMTs) for pediatric use. Six different excipients were tested as diluents. The properties of powder mixtures were evaluated before direct compression and pharmacotechnical tests were performed on the final formulation. The determination of the API content, uniformity of dosage, and physicochemical stability studies were analyzed by an HPLC-UV method. : The developed ODMTs met pharmacopeia specifications for content, hardness, friability, disintegration, and dissolution tests. The physicochemical stability study performed over 18 months shows that API content remains within 90.0-110.0% at least for this period. These ODMTs will allow efficient, safe, and high-quality pharmacotherapy.
三十多年来,苯海索(THP)一直被广泛用作治疗节段性和全身性肌张力障碍患者的儿科药物疗法。为了对这一人群实现有效且安全的药物治疗,需要新的制剂。这项工作的目的是开发用于儿科的苯海索口腔崩解片(ODMTs)。测试了六种不同的辅料作为稀释剂。在直接压片前评估了粉末混合物的性质,并对最终制剂进行了药物工艺测试。采用高效液相色谱 - 紫外法分析了原料药含量的测定、剂量均匀性和理化稳定性研究。:所开发的口腔崩解片在含量、硬度、脆碎度、崩解和溶出度测试方面符合药典规格。进行了18个月的理化稳定性研究表明,至少在此期间原料药含量保持在90.0 - 110.0% 范围内。这些口腔崩解片将实现高效、安全和高质量的药物治疗。