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Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice

A challenge in the development of dry powder formulations for inhalation is the poor reproducibility of their administration to small laboratory animals. The currently used devices for the pulmonary administration of dry powder formulations to small rodents often function sub-optimally as they use t...

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Autores principales: Heida, Rick, Hagedoorn, Paul, van Meel, Melle C., Prins, Jurrie E. R., Simonis, Frederike S., Akkerman, Renate, Huckriede, Anke L. W., Frijlink, Henderik W., de Boer, Anne H., Hinrichs, Wouter L. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385055/
https://www.ncbi.nlm.nih.gov/pubmed/37514034
http://dx.doi.org/10.3390/pharmaceutics15071847
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author Heida, Rick
Hagedoorn, Paul
van Meel, Melle C.
Prins, Jurrie E. R.
Simonis, Frederike S.
Akkerman, Renate
Huckriede, Anke L. W.
Frijlink, Henderik W.
de Boer, Anne H.
Hinrichs, Wouter L. J.
author_facet Heida, Rick
Hagedoorn, Paul
van Meel, Melle C.
Prins, Jurrie E. R.
Simonis, Frederike S.
Akkerman, Renate
Huckriede, Anke L. W.
Frijlink, Henderik W.
de Boer, Anne H.
Hinrichs, Wouter L. J.
author_sort Heida, Rick
collection PubMed
description A challenge in the development of dry powder formulations for inhalation is the poor reproducibility of their administration to small laboratory animals. The currently used devices for the pulmonary administration of dry powder formulations to small rodents often function sub-optimally as they use the same puff of air for both powder dispersion and aerosol delivery. As a result, either the air volume and flow rate are too low for complete powder deagglomeration or they are too high for effective aerosol delivery to the lungs of the animal. Therefore, novel and better devices are desired. We here present an aerosol generator designed to administer a pre-generated aerosol to the lungs of mice. By mapping the complex relationship between the airflow rate, delivery time and emitted dose, we were able to control the amount of powder being delivered from the aerosol generator. The emitted aerosol had a size range favorable for lung deposition and could be measured reproducibly. Nevertheless, in vivo fluorescent imaging still revealed considerable differences between the mice in terms of the dose deposited and the distribution of powder over the lungs, suggesting that a certain biological variation in lung deposition is inevitable.
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spelling pubmed-103850552023-07-30 Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice Heida, Rick Hagedoorn, Paul van Meel, Melle C. Prins, Jurrie E. R. Simonis, Frederike S. Akkerman, Renate Huckriede, Anke L. W. Frijlink, Henderik W. de Boer, Anne H. Hinrichs, Wouter L. J. Pharmaceutics Article A challenge in the development of dry powder formulations for inhalation is the poor reproducibility of their administration to small laboratory animals. The currently used devices for the pulmonary administration of dry powder formulations to small rodents often function sub-optimally as they use the same puff of air for both powder dispersion and aerosol delivery. As a result, either the air volume and flow rate are too low for complete powder deagglomeration or they are too high for effective aerosol delivery to the lungs of the animal. Therefore, novel and better devices are desired. We here present an aerosol generator designed to administer a pre-generated aerosol to the lungs of mice. By mapping the complex relationship between the airflow rate, delivery time and emitted dose, we were able to control the amount of powder being delivered from the aerosol generator. The emitted aerosol had a size range favorable for lung deposition and could be measured reproducibly. Nevertheless, in vivo fluorescent imaging still revealed considerable differences between the mice in terms of the dose deposited and the distribution of powder over the lungs, suggesting that a certain biological variation in lung deposition is inevitable. MDPI 2023-06-28 /pmc/articles/PMC10385055/ /pubmed/37514034 http://dx.doi.org/10.3390/pharmaceutics15071847 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Heida, Rick
Hagedoorn, Paul
van Meel, Melle C.
Prins, Jurrie E. R.
Simonis, Frederike S.
Akkerman, Renate
Huckriede, Anke L. W.
Frijlink, Henderik W.
de Boer, Anne H.
Hinrichs, Wouter L. J.
Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title_full Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title_fullStr Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title_full_unstemmed Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title_short Performance Testing of a Homemade Aerosol Generator for Pulmonary Administration of Dry Powder Formulations to Mice
title_sort performance testing of a homemade aerosol generator for pulmonary administration of dry powder formulations to mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10385055/
https://www.ncbi.nlm.nih.gov/pubmed/37514034
http://dx.doi.org/10.3390/pharmaceutics15071847
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