4.5 Article

Advancement of the Infant Air-Jet Dry Powder Inhaler (DPI): Evaluation of Different Positive-Pressure Air Sources and Flow Rates

期刊

PHARMACEUTICAL RESEARCH
卷 38, 期 9, 页码 1615-1632

出版社

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-021-03094-w

关键词

high efficiency aerosolization; infant DPI; inline DPI; nose-to-lung aerosol delivery; positive pressure DPI; trans-nasal aerosol delivery

资金

  1. Eunice Kennedy Shriver National Institute of Child Health & Human Development of the National Institutes of Health [R01HD087339]
  2. National Heart, Lung and Blood Institute of the National Institutes of Health [R01HL139673]

向作者/读者索取更多资源

This study aimed to improve the delivery of dry powder aerosol formulations to infants' lungs using an infant air-jet platform. Different air sources, flow rates, and pulmonary mechanics were explored, with the D1-Single air-jet DPI showing improved performance across various air sources. Lowering the flow rate increased lung delivery efficiency, unaffected by downstream pulmonary mechanics.
Purpose In order to improve the delivery of dry powder aerosol formulations to the lungs of infants, this study implemented an infant air-jet platform and explored the effects of different air sources, flow rates, and pulmonary mechanics on aerosolization performance and aerosol delivery through a preterm nose-throat (NT) in vitro model. Methods The infant air-jet platform was actuated with a positive-pressure air source that delivered the aerosol and provided a full inhalation breath. Three different air sources were developed to provide highly controllable positive-pressure air actuations (using actuation volumes of similar to 10 mL for the preterm model). While providing different flow waveform shapes, the three air sources were calibrated to produce the same flow rate magnitude (Q90: 90th percentile of flow rate). Multiple air-jet DPI designs were coupled with the air sources and evaluated with a model spray-dried excipient enhanced growth formulation. Results Compared to other designs, the D1-Single air-jet DPI provided improved performance with low variability across all three air sources. With the tested D1-Single air-jet and Timer air source, reducing the flow rate from 4 to 1.7 L/min marginally decreased the aerosol size and significantly increased the lung delivery efficiency above 50% of the loaded dose. These results were not impacted by the presence of downstream pulmonary mechanics (resistance and compliance model). Conclusions The selected design was capable of providing an estimated >50% lung delivery efficiency of a model spray-dried formulation and was not influenced by the air source, thereby enabling greater flexibility for platform deployment in different environments.

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