全身循环
药物输送
多孔性
气溶胶
纳米技术
粒子(生态学)
沉积(地质)
材料科学
粒径
空气动力学
药品
颗粒沉积
航程(航空)
化学
化学工程
医学
航空航天工程
复合材料
药理学
地质学
工程类
古生物学
有机化学
内科学
海洋学
沉积物
作者
Sachin Gharse,Jennifer Fiegel
标识
DOI:10.2174/1381612822666160128145356
摘要
The deep lungs provide an efficient pathway for drugs to transport into the systemic circulation, as the extremely large surface area and thin epithelial membrane enable rapid drug transport to the blood stream. To penetrate into the deep lungs, aerosol particles with aerodynamic diameters of 1-3 µm are optimal. Large porous hollow particles (LPHPs) can achieve this aerodynamic size range through enhanced porosity within the particles (typically < 0.4 g/cm(3)), which aerodynamically balances the large particle size (> 5 µm, up to 30 µm). The physical properties of these particles provide some key advantages compared to their small, nonporous counterparts through enhanced dispersibility, efficient deep lung deposition, and avoidance of phagocytic clearance. This review highlights the potential of LPHPs in pulmonary delivery of systemic drugs, with a focus on their critical attributes and key formulation aspects. In addition, three examples of LPHPs under development are presented to emphasize the potential of this technology to treat systemic diseases.
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