Department of Pharmaceutics and Biopharmacy, Philipps-Universität Marburg, Marburg, Germany.
Eur J Pharm Biopharm. 2011 May;78(1):90-6. doi: 10.1016/j.ejpb.2010.12.002. Epub 2010 Dec 7.
Spray-drying was investigated for the stabilization of surfactant-free nanoparticles as carriers for dry-powder inhalers. The microparticles rapidly dissolve after inhalation yielding dispersed nanoparticles. Nanoparticles were prepared by a solvent displacement technique avoiding any surfactants. Microcarriers were prepared by spray-drying nanoparticle suspensions with lactose, mannitol or α-cyclodextrin as stabilizers. Nanoparticle size and ζ-potential before and after spray-drying were analyzed with photon correlation spectroscopy and laser Doppler anemometry, respectively. Cell uptake into macrophages was studied using U 937 cells by confocal microscopy. Stabilization of nanoparticle suspensions by spray-drying with α-cyclodextrin yielded redispersible particles smaller than 200 nm. α-Cyclodextrin was a more efficient stabilizer than commonly used excipients. Microparticles with a mass median aerodynamic diameter of 4.3 μm showed properties suitable for dry-powder inhalation. The cell culture experiments with redispersed nanoparticles seem to suggest less interaction and uptake with macrophages compared to polymeric microparticles. In conclusion, nanoparticles can easily be transferred to dry-powders suitable for inhalation by spray-drying. This allows the pulmonary application of nanoparticles in high concentrations.
喷雾干燥法被用于稳定无表面活性剂的纳米颗粒作为干粉吸入剂的载体。吸入后,这些微粒迅速溶解,释放出分散的纳米颗粒。纳米颗粒通过溶剂置换技术制备,避免使用任何表面活性剂。微载体通过喷雾干燥纳米颗粒悬浮液与乳糖、甘露醇或 α-环糊精作为稳定剂来制备。喷雾干燥前后的纳米颗粒粒径和 ζ-电位分别用光子相关光谱法和激光多普勒测速法进行分析。通过共聚焦显微镜研究 U937 细胞中的细胞摄取。用 α-环糊精喷雾干燥稳定纳米颗粒悬浮液可得到小于 200nm 的再分散颗粒。α-环糊精是一种比常用赋形剂更有效的稳定剂。质量中值空气动力学直径为 4.3μm 的微颗粒具有适合干粉吸入的特性。与聚合物微颗粒相比,再分散纳米颗粒的细胞培养实验似乎表明与巨噬细胞的相互作用和摄取较少。总之,纳米颗粒可以很容易地通过喷雾干燥转化为适合吸入的干粉,从而可以在高浓度下将纳米颗粒应用于肺部。