Lafuente Yanina de, García Mónica Cristina, Jiminez-Kairuz Alvaro
Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Quimicas, Universidad Nacional de Córdoba, Córdoba, Argentina.
Unidad de Investigación y Desarrollo en Technologia Farmacéutica (UNITEFA), CONICET-UNC, Córdoba, Argentina.
Int J Pharm Compd. 2019 Jul-Aug;23(4):324-331.
Indomethacin is used for off-label prescription for the treatment of patent ductus arteriosus in premature infants. In Argentina, indomethacin is only available as a suppository, dermic cream, injectable ampules, and delayed-release capsules. Aiming to improve pediatric treatment and minimize the risk associated with improper dosage, this work focused on the development of an extemporaneous 0.2% indomethacin oral suspension, starting from the commercially injectable formulation. Two 150-mL batches of suspension were prepared using Generally Recognized as Safe excipients. The suspensions were stored for 17 days at room temperature. Physical stability, morphological analysis of suspended particles, sedimentation volume, easy re-suspension, and dynamic viscosity were studied. The indomethacin content, dissolution studies, and microbiological attributes of nonsterile pharmaceutical products were also evaluated. After 17 days of storage, the suspension was easily re-dispersed after 15 seconds of the hand-shaking technique. There were no detectable changes in color, odor, and/or flavor. The suspension showed minimal changes in pH, viscosity, shape, and mean size of the suspended indomethacin particles. The content uniformity and drug dissolution remained within the acceptable range during storage. This oral liquid suspension is an interesting alternative to be prepared by hospital pharmacy services for optimizing the pediatric treatment of patent ductus arteriosus.
吲哚美辛被用于早产儿动脉导管未闭的超说明书用药处方。在阿根廷,吲哚美辛仅有栓剂、乳膏剂、注射用安瓿和缓释胶囊等剂型。为改善儿科治疗并将不当剂量相关风险降至最低,本研究从市售注射用制剂出发,致力于开发一种临时配制的0.2%吲哚美辛口服混悬液。使用公认安全的辅料制备了两批150毫升的混悬液。将混悬液在室温下储存17天。研究了其物理稳定性、混悬颗粒的形态分析、沉降体积、易再混悬性和动态粘度。还评估了非无菌药品的吲哚美辛含量、溶出度研究和微生物学特性。储存17天后,通过手摇技术,混悬液在15秒后易于重新分散。颜色、气味和/或味道未检测到变化。混悬液在pH值、粘度、形状和吲哚美辛混悬颗粒平均大小方面变化极小。储存期间,含量均匀度和药物溶出度仍在可接受范围内。这种口服液体混悬液是医院药房服务为优化动脉导管未闭儿科治疗而配制的一种有趣的替代选择。