Pangeni Rudra, Hassan Amr Ali Mohamed, Farkas Dale, Sudarjat Hadi, Longest Worth, Hindle Michael, Xu Qingguo
Department of Pharmaceutics, Virginia Commonwealth University, Richmond, Virginia 23298, United States.
Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
Mol Pharm. 2023 Apr 3;20(4):2207-2216. doi: 10.1021/acs.molpharmaceut.3c00007. Epub 2023 Mar 20.
Pulmonary deposition of lung-targeted therapeutic aerosols can achieve direct drug delivery to the site of action, thereby enhancing the efficacy and reducing systemic exposure. In this study, we investigated the in vitro and in vivo aerosol performance of the novel small animal air-jet dry powder insufflator (Rat AJ DPI) using spray-dried albuterol excipient-enhanced-growth (EEG) powder as a model formulation. The in vitro aerosolization performance of the optimized albuterol EEG powder was first assessed using the Rat AJ DPI. The performance of Rat AJ DPI to deliver albuterol EEG aerosol to rat lungs was then compared to that of the Penn-Century Insufflator. Albuterol EEG powders dispersed using the Rat AJ DPI demonstrated narrow unimodal aerosol size distribution profiles, which were independent of the loaded powder dose (1, 2, and 5 mg). In addition, the span value for Rat AJ DPI (5 mg powder mass) was 1.32, which was 4.2-fold lower than that for Penn-Century insufflator (5 mg powder mass). At a higher loaded mass of 5 mg, the Rat AJ DPI delivered significantly larger doses to rat lungs compared with the Penn-Century DPI. The Rat AJ DPI with hand actuation delivered approximately 85% of the total emitted dose (2 and 5 mg loadings), which was comparatively higher than that for Penn-Century DPI (approximately 75%). In addition, percentage deposition in each of the lung lobes for the Rat AJ DPI was observed to be independent of the administration dose (2 and 5 mg loadings) with coefficients of variation below 12%, except in the right middle lobe. Automatic actuation of a 5 mg powder mass using the Rat AJ DPI demonstrated a similar delivered dose compared to manual actuation of the same dose, with 82% of the total emitted dose reaching the lung lobes. High-efficiency delivery of the aerosol to the lobar lung region and low sensitivity of the interlobar delivery efficiency to the loaded dose highlight the suitability of the new air-jet DPI for administering therapeutic pharmaceutical aerosols to small test animals.
肺靶向治疗气雾剂的肺部沉积可实现药物直接递送至作用部位,从而提高疗效并减少全身暴露。在本研究中,我们以喷雾干燥的沙丁胺醇辅料增强生长(EEG)粉末作为模型制剂,研究了新型小动物空气喷射干粉吸入器(大鼠AJ DPI)的体外和体内气雾剂性能。首先使用大鼠AJ DPI评估优化后的沙丁胺醇EEG粉末的体外雾化性能。然后将大鼠AJ DPI向大鼠肺部递送沙丁胺醇EEG气雾剂的性能与宾夕法尼亚世纪吸入器的性能进行比较。使用大鼠AJ DPI分散的沙丁胺醇EEG粉末显示出狭窄的单峰气雾剂粒径分布曲线,且与装载的粉末剂量(1、2和5毫克)无关。此外,大鼠AJ DPI(5毫克粉末质量)的跨度值为1.32,比宾夕法尼亚世纪吸入器(5毫克粉末质量)低4.2倍。在5毫克的较高装载质量下,与宾夕法尼亚世纪干粉吸入器相比,大鼠AJ DPI向大鼠肺部递送的剂量明显更大。手动操作的大鼠AJ DPI递送了约85%的总发射剂量(2毫克和5毫克装载量),相对高于宾夕法尼亚世纪干粉吸入器(约75%)。此外,观察到大鼠AJ DPI在每个肺叶中的沉积百分比与给药剂量(2毫克和5毫克装载量)无关,变异系数低于12%,右中叶除外。使用大鼠AJ DPI对5毫克粉末质量进行自动操作显示出与相同剂量手动操作相似的递送剂量,总发射剂量的82%到达肺叶。气雾剂向肺叶区域的高效递送以及叶间递送效率对装载剂量的低敏感性突出了新型空气喷射干粉吸入器用于向小型实验动物给药治疗性药物气雾剂的适用性。