沉积(地质)
气溶胶
生物物理学
肺
粒子(生态学)
化学
气道
颗粒沉积
分区(防火)
纳米技术
高分辨率
体积热力学
肺泡
人肺
囊性纤维化
荧光显微镜
解剖
材料科学
生物医学工程
纤维化
车辆段
空气空间
纳米颗粒
病理
体视学
方向(向量空间)
肺表面活性物质
流量(数学)
作者
Gabrielle N. Grifno,Han Ali Kahvecioglu,Robert LeBourdais,Victoria Travnik,Rohin Banerji,Winita Wangsrikhun,Linzheng Shi,Suleyman B. Bozal,H Suh,Ahmed Raslan,Athanasios Batgidis,Byungjun Kang,F Deng,Caleb Dalton,Andrew Tsao,Lauren Castle,Kathryn Regan,Abdulrahman Kobayter,Michael Vannini,M Rashidian
标识
DOI:10.1038/s41551-026-01724-5
摘要
Inhaled pathogens, pollutants and therapeutics interact with the dynamic architecture of the alveoli, yet how individual particles move and deposit at cellular resolution remains unclear. Here, utilizing the crystal ribcage platform, we track aerosol transport in ex vivo, actively ventilated lungs using real-time fluorescence imaging with single-particle resolution, capturing droplet trajectories, free-flight motion, impact orientation and deposition timescales within functional alveoli. These measurements show that intra-alveolar transport is directional and shaped by airway-guided flow and tissue motion. At larger scales, aerosols do not disperse uniformly throughout the lung's volume but instead concentrate into geometrically constrained clusters of alveoli, forming a conserved mosaic-like compartmentalization while neighbouring alveoli remain largely unexposed. The pattern persists across particle types and species and varies with particle properties and lung age. In models of emphysema, fibrosis and metastasis, airway remodelling alters both the geometry and amount of deposition. These multiscale insights reveal how single-particle transport and airway structure together shape alveolar exposure, immune activation, development and therapeutic accessibility.
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