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Published on: April 6, 2017
Targeted delivery of inhalable drug particles in a patient-specific tracheobronchial tree with moderate COVID-19: A
Jianwei Wang1, Ya Zhang2, Xiaole Chen1
1School of Energy and Mechanical Engineering, Nanjing Normal University, Nanjing, Jiangsu 210046, China.
Abstract:
The coronavirus disease 2019 (COVID-19) pandemic has led to severe social and economic disruption worldwide. Although currently no consent has been reached on a specific therapy that can treat COVID-19 effectively, several inhalation therapy strategies have been proposed to inhibit SARS-CoV-2 infection. These strategies include inhalations of antiviral drugs, anti-inflammatory drugs, and vaccines. To investigate how to enhance the therapeutic effect by increasing the delivery efficiency (DE) of the inhaled aerosolized drug particles, a patient-specific tracheobronchial (TB) tree from the trachea up to generation 6 (G6) with moderate COVID-19 symptoms was selected as a testbed for the in silico trials of targeted drug delivery to the lung regions with pneumonia alba, i.e., the severely affected lung segments (SALS). The 3D TB tree geometry was reconstructed from spiral computed tomography (CT) scanned images. The airflow field and particle trajectories were solved using a computational fluid dynamics (CFD) based Euler-Lagrange model at an inhalation flow rate of 15 L/min. Particle release maps, which record the deposition locations of the released particles, were obtained at the inlet according to the particle trajectories. Simulation results show that particles with different diameters have similar release maps for targeted delivery to SALS. Point-source aerosol release (PSAR) method can significantly enhance the DE into the SALS. A C++ program has been developed to optimize the location of the PSAR tube. The optimized simulations indicate that the PSAR approach can at least increase the DE of the SALS by a factor of 3.2× higher than conventional random-release drug-aerosol inhalation. The presence of the PSAR tube only leads to a 7.12% change in DE of the SALS. This enables the fast design of a patient-specific treatment for reginal lung diseases.
Insights
A new point-source aerosol release (PSAR) method significantly enhances drug delivery efficiency to severely affected lung segments in COVID-19 patients. This targeted inhalation strategy improves treatment for regional lung diseases.
Area of Science:
- Pulmonary Drug Delivery
- Computational Fluid Dynamics
- Medical Imaging
Background:
- The COVID-19 pandemic highlighted the need for effective inhalation therapies.
- Current strategies for delivering drugs to the lungs face challenges in efficiency.
- Targeting drug delivery to specific lung regions, like those affected by pneumonia alba, is crucial for treating severe COVID-19.
Purpose of the Study:
- To investigate methods for enhancing drug delivery efficiency (DE) in the tracheobronchial tree.
- To evaluate the effectiveness of a point-source aerosol release (PSAR) method for targeted drug delivery to severely affected lung segments (SALS).
- To develop a patient-specific computational model for optimizing inhalation therapy.
Main Methods:
- Reconstructed a patient-specific 3D tracheobronchial (TB) tree from CT scans.
- Employed a computational fluid dynamics (CFD) based Euler-Lagrange model to simulate airflow and particle trajectories.
- Developed a C++ program to optimize the PSAR tube placement for targeted delivery.
Main Results:
- Particle release maps indicated similar deposition patterns for various particle sizes.
- The PSAR method demonstrated a significant enhancement in DE to SALS compared to conventional methods.
- Optimized PSAR increased DE to SALS by at least 3.2 times.
- The PSAR tube minimally impacted overall DE (7.12% change).
Conclusions:
- The PSAR method offers a substantial improvement in targeted drug delivery to SALS.
- This approach enables rapid design of patient-specific inhalation treatments for regional lung diseases.
- Optimized PSAR represents a promising strategy for enhancing the efficacy of lung-targeted therapies.
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