干粉吸入器
乳糖
气溶胶化
化学工程
流态化
材料科学
流变学
吸入
化学
气动直径
色谱法
流化床
气溶胶
复合材料
食品科学
吸入器
有机化学
医学
哮喘
内科学
工程类
解剖
作者
Ying Sun,Qin Lu,Jiayi Li,Jian Su,Ruxiao Song,Xin Zhang,Jian Guan,Shirui Mao
出处
期刊:Aaps Journal
[Springer Science+Business Media]
日期:2021-04-15
卷期号:23 (3)
被引量:16
标识
DOI:10.1208/s12248-021-00582-0
摘要
Dry powder inhaler (DPI) is recognized as the first choice for lung diseases’ treatment. However, it lacks a universal way for DPI formulation development. Fine lactose is commonly added in DPIs to improve delivery performance; however, the fine ratio-dependent mechanism is unclear. Therefore, the objective of this study is to explore the influence of fine lactose ratio on DPI powder properties and aerodynamic behavior, and the fine lactose ratio-dependent mechanism involved during powder fluidization and lung deposition. Here salbutamol sulfate was used as a model drug, Lactohale® 206 as coarse carrier, and Lactohale® 300 as fine component; the mixtures were prepared at 1% drug content, with fine content up to 20%. It was shown that with the fine addition, flowability of the mixtures was improved, interaction among particles was increased, and the presence of fines could help to improve DPI’s aerosolization performance. When the fines added were less than 3%, the “active site” hypothesis played a leading role. When the added fines were over 3% but less than 10%, fluidization enhancement mechanism was more important. After the added fines reaching 10%, aggregate mechanism started to dominate. However, FPF cannot be further increased once the fines reached 20%. Moreover, the correlations between FPF and dynamic powder parameters were verified in ternary mixtures, and cohesion had a greater impact on FPF than that of flowability. In conclusion, adding lactose fines is an effective way to improve lung deposition of DPI, with the concrete mechanism lactose fine ratio dependent.Graphical abstract
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