The determination of the particle dynamics in the human acinar airways having millions of
alveoli is critical in preventing potential health problems and delivering therapeutic
particles effectively to target locations. Despite its complex geometrical structure and
complicate wall movements, the advanced calculation simulations can provide valuable
results to accurately predict the aerosol deposition in this region. The objective of this
study was to numerically investigate the aerosol particle transport and deposition in the
intra-acinar region of a human lung for different breathing scenarios (i.e., light,
normal, and heavy activities) during multiple breaths. Idealized intra-acinar models
utilized in this study consisted of a respiratory bronchial model, an alveolar duct model,
and an alveolar sac model. The particles with 5
μ
m in diameter released
from the inlet of the model were tracked until they deposited or escaped from the
computational domain. The results showed that due to the rhythmic alveolar wall movement,
the flow field was divided into two regions: one is the low-speed alveolar flow and the
other is the channel flow. It was found that the chaotic acinar flow irreversibility
played a significant role in the aerosol transport in higher generations. During the
succeeding breaths, more particles deposited or escaped to the relating acinar generation
and reached the more distal regions of the lung. The number of particles remaining in the
suspension at the end of the third cycle ranged from 0.016% to 3%. When the mouth flow
rate increased, the number of particles remaining in the suspension reduced, resulting in
higher deposition efficiency. The total deposition efficiencies for each flow rate were
24%, 47%, and 77%, respectively. The particle simulation results also showed that more
breathing cycle was required for full aerosol particle deposition or escape from the
model. In addition to the alveolar wall motion, the type of breathing condition and
breathing cycle had a significant effect on the accurate prediction of the aerosol
deposition in the intra-acinar region of the human lung.