Baratta Francesca, Zingarelli Chiara, Fanton Federica, Lamy Editson, Di Lascio Gaetano, Brusa Paola
Department of Drug Science and Technology, University of Turin, Via Pietro Giuria 9, 10125 Turin, Italy.
Aid Progress Pharmacist Agreement Non-Profit Association, Via Pietro Giuria 9, 10125 Turin, Italy.
Pharmaceutics. 2025 Jun 17;17(6):787. doi: 10.3390/pharmaceutics17060787.
The paediatric population is a heterogenous group that is known to be a therapeutic orphan despite the recent incentives to promote the development of children's formulations. Especially in low and middle-income countries, there is still a worldwide shortfall for the treatment and prevention of a variety of paediatric conditions. In this context, we developed a formulation specifically intended to administer metronidazole to paediatric patients using basic and low-cost excipients and with a simple set-up method. . Various mixtures of excipients were prepared to obtain a suitable metronidazole liquid formulation at a concentration of 250 mg/5 mL. The best formula was tested for its quality and stability, assessing the uniformity of content, the pH, and the dispersion quality. We evaluated the stability of the preparation for 180 days at room temperature (25 +/- 2 °C), in a thermostatic oven (40 +/- 2 °C), and in a fridge (4 +/- 2 °C). The tests performed gave excellent results. No variation greater than 10% was detected in the metronidazole concentration or in pH values after 180 days regardless of the temperature conditions during storage. Moreover, the microscope analysis confirmed the absence of significant differences over time. The results were consistent in different environmental conditions, ensuring the possibility of using the formulation even in those tropical countries where is not always possible to guarantee the conservation of medicines in controlled conditions. Moreover, the simple composition and easy preparation procedure make it possible to produce the suspension in any context, ensuring the quality of the finished product.
儿科人群是一个异质性群体,尽管最近有促进儿童制剂开发的激励措施,但该群体仍被视为治疗孤儿。特别是在低收入和中等收入国家,全球在治疗和预防各种儿科疾病方面仍存在缺口。在此背景下,我们开发了一种制剂,专门用于使用基本且低成本的辅料以及简单的配制方法向儿科患者施用甲硝唑。制备了各种辅料混合物,以获得浓度为250mg/5mL的合适甲硝唑液体制剂。对最佳配方进行了质量和稳定性测试,评估了含量均匀度、pH值和分散质量。我们在室温(25±2°C)、恒温箱(40±2°C)和冰箱(4±2°C)中对该制剂的稳定性进行了180天的评估。所进行的测试给出了优异的结果。无论储存期间的温度条件如何,180天后甲硝唑浓度或pH值的变化均未超过10%。此外,显微镜分析证实随时间推移没有显著差异。在不同环境条件下结果一致,确保了即使在那些无法始终保证在受控条件下保存药品的热带国家也有可能使用该制剂。此外,简单的成分和易于制备的程序使得能够在任何环境下生产该混悬液,确保了成品的质量。