含有高剂量难溶疏水药物的吸入用干粉制剂

T. Tarara, Danforth P Miller, Audrey E. Weers, Ariel R. Muliadi, J. Tso, A. Eliahu, J. Weers
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引用次数: 6

摘要

采用悬浮- pulmosphere™技术制备疏水结晶药物GDC-A喷雾干燥制剂。药物负荷的增加导致初级粒径分布的减小和疏通密度的增加。这使得使用便携式干粉吸入器从3号胶囊中获得高达25毫克的细颗粒剂量成为可能。粉末在物理和化学上都是稳定的,在加工过程中或在40°C的开放式环境中储存1个月,没有观察到物理形态的变化或降解。讨论了基于悬浮液的喷雾干燥工艺相对于基于溶液的喷雾干燥工艺在稳定性、肺靶向性和安全性/耐受性方面的潜在优势。
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Formulation of Dry Powders for Inhalation Comprising High Doses of a Poorly Soluble Hydrophobic Drug
Spray-dried formulations of a hydrophobic, crystalline drug, GDC-A, were prepared using the suspension-PulmoSphere™ technology. Increases in drug loading resulted in decreases in the primary particle size distribution and increases in tapped density. This enabled fine particle doses of up to 25 mg to be achieved with a portable dry powder inhaler from a size three capsule. The powders were physically and chemically stable, with no changes in physical form or degradants observed during processing or on storage in an open configuration at 40°C for 1 month. The potential benefits of the suspension-based spray drying process relative to solution-based spray drying in terms of stability, lung targeting, and safety/tolerability are discussed.
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