Computational optimization of spatial drug release to enhance inhaled particle deposition in human upper and central airways

Journal Article (2026)
Author(s)

Ruipeng Xu ( J.M. Burgerscentrum Research School for Fluid Mechanics, TU Delft - Applied Sciences)

Jiaqi Fan (Jiangsu Engineering Research Center of Dust Control and Occupational Protection, China University of Mining and Technology)

Xueren Li (China University of Mining and Technology, Jiangsu Engineering Research Center of Dust Control and Occupational Protection, Royal Melbourne Institute of Technology University)

J. Ruud van Ommen (TU Delft - Applied Sciences)

Yidan Shang (Fudan University, Shanghai University of Engineering Science)

Saša Kenjereš ( J.M. Burgerscentrum Research School for Fluid Mechanics, TU Delft - Applied Sciences)

Research Group
ChemE/Transport Phenomena
DOI related publication
https://doi.org/10.1016/j.powtec.2026.122688 Final published version
More Info
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Publication Year
2026
Language
English
Research Group
ChemE/Transport Phenomena
Journal title
Powder Technology
Volume number
481
Article number
122688
Downloads counter
3
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Abstract

Inhaled drug delivery is a promising strategy for the rapid treatment of respiratory diseases due to its direct targeting of the pulmonary system. Nevertheless, challenges remain in optimizing deposition efficiency, particularly in reaching deeper lung generations and achieving directional control of particle transport. To achieve effective deep-lung aerosol delivery, the present proof-of-concept study proposes computational optimization of particle release strategies. Both non-invasive and invasive approaches are explored, with particular emphasis on release concentration and spatial positioning. Numerical simulations are conducted using a previously validated subject-specific mouth-to-lung model reconstructed from high-resolution Computed Tomography (CT) scans, ensuring anatomical realism and geometrical reproducibility. The results show that concentrated non-invasive release at the mouth plane improves particle penetration through the constricted laryngeal region. Meanwhile, invasive strategies involving focused delivery (such as catheter-based injection) lead to enhanced deposition in the deeper lung regions. Notably, directional control of deposition was preliminarily achieved, with particles preferentially targeting either the left or right lung lobe based on the injection position, offering new potential for site-specific therapy. It is concluded that the presented computational framework can provide detailed insights for optimizing particle transport and deposition in specific lung regions. These detailed insights could provide valuable information for developing novel clinical treatments for respiratory diseases.