Department of Pharmaceutics, Virginia Commonwealth University, Richmond, VA, USA.
Department of Pediatrics, Children's Hospital of Richmond, Virginia Commonwealth University, Richmond, VA, USA.
Nanomedicine. 2020 Oct;29:102262. doi: 10.1016/j.nano.2020.102262. Epub 2020 Jul 3.
Tenacious sputum poses a critical diffusion barrier for aerosol antibiotics used to treat cystic fibrosis (CF) lung infection. We conducted a proof-of-concept study using dense poly(ethylene glycol) coated polystyrene nanoparticles (PS-PEG NPs) as model muco-inert particles (MIPs) formulated as a powder using an excipient enhanced growth (EEG) strategy, aiming to minimize extrathoracic airway loss, maximize deposition in the airway and further overcome the sputum barrier in the CF lungs. The EEG aerosol formulation containing PS-PEG MIPs was prepared by spray drying and produced discrete spherical particles with geometric diameter of approximately 2 μm; and >80% of the powder dose was delivered from a new small-animal dry powder inhaler (DPI). The MIPs released from the EEG aerosol had human airway mucus and CF sputum diffusion properties comparable to the suspension formulation. These properties make this formulation a promising pulmonary drug delivery system for CF lung infections.
粘稠的痰液是治疗囊性纤维化 (CF) 肺部感染的气溶胶抗生素的一个关键扩散屏障。我们使用密集的聚乙二醇 (PEG) 涂层聚苯乙烯纳米颗粒 (PS-PEG NPs) 作为模型抗粘液粒子 (MIPs) 进行了概念验证研究,这些 MIPs 被制成粉末,采用赋形剂增强生长 (EEG) 策略,旨在最大限度地减少胸外气道损失,最大限度地将药物沉积在气道中,并进一步克服 CF 肺部中的痰液屏障。含有 PS-PEG MIP 的 EEG 气溶胶制剂通过喷雾干燥制备,产生的离散球形颗粒的几何直径约为 2 μm;并且新的小动物干粉吸入器 (DPI) 输送了超过 80%的粉末剂量。从 EEG 气溶胶中释放的 MIPs 具有与人气道粘液和 CF 痰液扩散特性相当的悬浮制剂。这些特性使这种制剂成为治疗 CF 肺部感染的有前途的肺部药物递送系统。