Aziz Shahir, Scherlieβ Regina, Steckel Hartwig
Department of Pharmaceutical Technology, Faculty of Pharmacy, German University in Cairo, Cairo 11835, Egypt.
Department of Pharmaceutics and Biopharmaceutics, Kiel University, D-24118 Kiel, Germany.
Pharmaceutics. 2020 Nov 27;12(12):1154. doi: 10.3390/pharmaceutics12121154.
Oseltamivir phosphate (OP) is an antiviral drug available only as oral therapy for the treatment of influenza and as a potential treatment option when in combination with other medication in the fight against the corona virus disease (COVID-19) pneumonia. In this study, OP was formulated as a dry powder for inhalation, which allows drug targeting to the site of action and potentially reduces the dose, aiming a more efficient therapy. Binary formulations were based on micronized excipient particles acting like diluents, which were blended with the drug OP. Different excipient types, excipient ratios, and excipient size distributions were prepared and examined. To investigate the feasibility of delivering high doses of OP in a single dose, 1:1, 1:3, and 3:1 drug/diluent blending ratios have been prepared. Subsequently, the aerosolization performance was evaluated for all prepared formulations by cascade impaction using a novel medium-resistance capsule-based inhaler (UNI-Haler). Formulations with micronized trehalose showed relatively excellent aerosolization performance with highest fine-particle doses in comparison to examined lactose, mannitol, and glucose under similar conditions. Focusing on the trehalose-based dry-powder inhalers' (DPIs) formulations, a physicochemical characterization of extra micronized grade trehalose in relation to the achieved performance in dispersing OP was performed. Additionally, an early indication of inhaled OP safety on lung cells was noted by the viability MTT assay utilizing Calu-3 cells.
磷酸奥司他韦(OP)是一种抗病毒药物,仅作为口服疗法用于治疗流感,并且在与其他药物联合用于对抗冠状病毒病(COVID-19)肺炎时作为一种潜在的治疗选择。在本研究中,OP被制成干粉吸入剂,这使得药物能够靶向作用部位并可能降低剂量,旨在实现更有效的治疗。二元制剂基于起稀释剂作用的微粉化辅料颗粒,其与药物OP混合。制备并检查了不同的辅料类型、辅料比例和辅料粒度分布。为了研究单剂量递送高剂量OP的可行性,制备了1:1、1:3和3:1的药物/稀释剂混合比例。随后,使用新型中阻力胶囊型吸入器(UNI-Haler)通过级联撞击对所有制备的制剂的雾化性能进行了评估。与在相似条件下检查的乳糖、甘露醇和葡萄糖相比,含有微粉化海藻糖的制剂显示出相对优异的雾化性能,细颗粒剂量最高。针对基于海藻糖的干粉吸入剂(DPI)制剂,对额外微粉化级海藻糖在分散OP方面所达到的性能进行了物理化学表征。此外,利用Calu-3细胞通过活力MTT测定法观察到了吸入OP对肺细胞安全性的早期迹象。