» Articles » PMID: 32451773

Development of Dry Powder Inhaler Patient Interfaces for Improved Aerosol Delivery to Children

Overview
Publisher Springer
Specialty Pharmacology
Date 2020 May 27
PMID 32451773
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The objective of this study was to explore different internal flow passages in the patient interface region of a new air-jet-based dry powder inhaler (DPI) in order to minimize device and extrathoracic aerosol depositional losses using computational fluid dynamics (CFD) simulations. The best-performing flow passages were used for oral and nose-to-lung (N2L) aerosol delivery in pediatric extrathoracic airway geometries consistent with a 5-year-old child. Aerosol delivery conditions were based on a previously developed and tested air-jet DPI device and included a base flow rate of 13.3 LPM (delivered from a small ventilation bag) and an inhaled air volume of 750 mL. Initial CFD models of the system clearly established that deposition on either the back of the throat or nasal cannula bifurcation was strongly correlated with the maximum velocity exiting the flow passage. Of all designs tested, the combination of a 3D rod array and rapid expansion of the flow passage side walls was found to dramatically reduce interface and device deposition and improve lung delivery of the aerosol. For oral aerosol administration, the optimal flow passage compared with a base case reduced device, mouthpiece, and mouth-throat deposition efficiencies by factors of 8-, 3-, and 2-fold, respectively. For N2L aerosol administration, the optimal flow pathway compared with a base case reduced device, nasal cannula, and nose-throat deposition by 16-, 6-, and 1.3-fold, respectively. In conclusion, a new patient interface design including a 3D rod array and rapid expansion dramatically improved transmission efficiency of a dry powder aerosol.

Citing Articles

Development of an Infant Air-Jet Dry Powder Aerosol Delivery System (iDP-ADS) Including a New Multifunctional Bifurcating Two-Prong Nasal Interface.

Strickler S, Farkas D, Momin M, Vargas L, Aladwani G, Hindle M Pharm Res. 2025; 42(2):365-384.

PMID: 39930310 PMC: 11880044. DOI: 10.1007/s11095-024-03814-y.


Characterization of Pediatric Extrathoracic Aerosol Deposition with Air-Jet Dry Powder Inhalers.

Thomas M, Bass K, Farkas D, Longest W J Aerosol Sci. 2025; 183.

PMID: 39830599 PMC: 11737425. DOI: 10.1016/j.jaerosci.2024.106474.


Leveraging Numerical Simulation Technology to Advance Drug Preparation: A Comprehensive Review of Application Scenarios and Cases.

Gu Q, Wu H, Sui X, Zhang X, Liu Y, Feng W Pharmaceutics. 2024; 16(10).

PMID: 39458634 PMC: 11511050. DOI: 10.3390/pharmaceutics16101304.


Dry powder inhaler design and particle technology in enhancing Pulmonary drug deposition: challenges and future strategies.

Islam N, Suwandecha T, Srichana T Daru. 2024; 32(2):761-779.

PMID: 38861247 PMC: 11555000. DOI: 10.1007/s40199-024-00520-3.


Development of an effective two-equation turbulence modeling approach for simulating aerosol deposition across a range of turbulence levels.

Jubaer H, Thomas M, Farkas D, Kolanjiyil A, Momin M, Hindle M J Aerosol Sci. 2024; 175:106262.

PMID: 38164243 PMC: 10698304. DOI: 10.1016/j.jaerosci.2023.106262.


References
1.
Bass K, Farkas D, Longest W . Optimizing Aerosolization Using Computational Fluid Dynamics in a Pediatric Air-Jet Dry Powder Inhaler. AAPS PharmSciTech. 2019; 20(8):329. PMC: 7324282. DOI: 10.1208/s12249-019-1535-4. View

2.
Longest P, Son Y, Holbrook L, Hindle M . Aerodynamic factors responsible for the deaggregation of carrier-free drug powders to form micrometer and submicrometer aerosols. Pharm Res. 2013; 30(6):1608-27. PMC: 3703624. DOI: 10.1007/s11095-013-1001-z. View

3.
Hindle M, Longest P . Quantitative analysis and design of a spray aerosol inhaler. Part 2: improvements in mouthpiece performance. J Aerosol Med Pulm Drug Deliv. 2012; 26(5):237-47. DOI: 10.1089/jamp.2012.0995. View

4.
Walenga R, Tian G, Hindle M, Yelverton J, Dodson K, Longest P . Variability in Nose-to-Lung Aerosol Delivery. J Aerosol Sci. 2014; 78:11-29. PMC: 4187112. DOI: 10.1016/j.jaerosci.2014.08.003. View

5.
Hansen S, Rau M, Krogh Johansen H, Ciofu O, Jelsbak L, Yang L . Evolution and diversification of Pseudomonas aeruginosa in the paranasal sinuses of cystic fibrosis children have implications for chronic lung infection. ISME J. 2011; 6(1):31-45. PMC: 3246239. DOI: 10.1038/ismej.2011.83. View