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Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration
Unpredictable outbreaks due to respiratory viral infections emphasize the need for new drug delivery strategies to the entire respiratory tract. As viral attack is not limited to a specific anatomic region, antiviral therapy that targets both the upper and lower respiratory tract would be most effec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958263/ https://www.ncbi.nlm.nih.gov/pubmed/35358643 http://dx.doi.org/10.1016/j.ijpharm.2022.121704 |
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author | Seow, Han Cong Liao, Qiuying Lau, Andy T.Y. Leung, Susan W.S. Yuan, Shuofeng Lam, Jenny K.W. |
author_facet | Seow, Han Cong Liao, Qiuying Lau, Andy T.Y. Leung, Susan W.S. Yuan, Shuofeng Lam, Jenny K.W. |
author_sort | Seow, Han Cong |
collection | PubMed |
description | Unpredictable outbreaks due to respiratory viral infections emphasize the need for new drug delivery strategies to the entire respiratory tract. As viral attack is not limited to a specific anatomic region, antiviral therapy that targets both the upper and lower respiratory tract would be most effective. This study aimed to formulate tamibarotene, a retinoid derivative previously reported to display broad-spectrum antiviral activity against influenza and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), as a novel dual particle size powder formulation that targets both the nasal cavity and the lung by a single route of intranasal administration. Spray freeze drying (SFD) and spray drying (SD) techniques were employed to prepare tamibarotene powder formulations, and cyclodextrin was used as the sole excipient to enhance drug solubility. With the employment of appropriate atomizing nozzles, particles of size above 10 μm and below 5 μm could be produced for nasal and lung deposition, respectively. The aerosol performance of the powder was evaluated using Next Generation Impactor (NGI) coupled with a glass expansion chamber and the powder was dispersed with a nasal powder device. By blending powder of two different particle sizes, a single powder formulation with dual aerosol deposition characteristic in both the nasal and pulmonary regions was produced. The aerosol deposition fractions in the nasal cavity and pulmonary region could be modulated by varying the powder mixing ratio. All dry powder formulations exhibited spherical structures, amorphous characteristics and improved dissolution profile as compared to the unformulated tamibarotene. Overall, a novel dual targeting powder formulation of tamibarotene exhibiting customizable aerosol deposition profile was developed. This exceptional formulation strategy can be adopted to deliver other antimicrobial agents to the upper and lower airways for the prevention and treatment of human respiratory infections. |
format | Online Article Text |
id | pubmed-8958263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89582632022-03-28 Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration Seow, Han Cong Liao, Qiuying Lau, Andy T.Y. Leung, Susan W.S. Yuan, Shuofeng Lam, Jenny K.W. Int J Pharm Article Unpredictable outbreaks due to respiratory viral infections emphasize the need for new drug delivery strategies to the entire respiratory tract. As viral attack is not limited to a specific anatomic region, antiviral therapy that targets both the upper and lower respiratory tract would be most effective. This study aimed to formulate tamibarotene, a retinoid derivative previously reported to display broad-spectrum antiviral activity against influenza and severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), as a novel dual particle size powder formulation that targets both the nasal cavity and the lung by a single route of intranasal administration. Spray freeze drying (SFD) and spray drying (SD) techniques were employed to prepare tamibarotene powder formulations, and cyclodextrin was used as the sole excipient to enhance drug solubility. With the employment of appropriate atomizing nozzles, particles of size above 10 μm and below 5 μm could be produced for nasal and lung deposition, respectively. The aerosol performance of the powder was evaluated using Next Generation Impactor (NGI) coupled with a glass expansion chamber and the powder was dispersed with a nasal powder device. By blending powder of two different particle sizes, a single powder formulation with dual aerosol deposition characteristic in both the nasal and pulmonary regions was produced. The aerosol deposition fractions in the nasal cavity and pulmonary region could be modulated by varying the powder mixing ratio. All dry powder formulations exhibited spherical structures, amorphous characteristics and improved dissolution profile as compared to the unformulated tamibarotene. Overall, a novel dual targeting powder formulation of tamibarotene exhibiting customizable aerosol deposition profile was developed. This exceptional formulation strategy can be adopted to deliver other antimicrobial agents to the upper and lower airways for the prevention and treatment of human respiratory infections. The Author(s). Published by Elsevier B.V. 2022-05-10 2022-03-28 /pmc/articles/PMC8958263/ /pubmed/35358643 http://dx.doi.org/10.1016/j.ijpharm.2022.121704 Text en © 2022 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Seow, Han Cong Liao, Qiuying Lau, Andy T.Y. Leung, Susan W.S. Yuan, Shuofeng Lam, Jenny K.W. Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title | Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title_full | Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title_fullStr | Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title_full_unstemmed | Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title_short | Dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
title_sort | dual targeting powder formulation of antiviral agent for customizable nasal and lung deposition profile through single intranasal administration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958263/ https://www.ncbi.nlm.nih.gov/pubmed/35358643 http://dx.doi.org/10.1016/j.ijpharm.2022.121704 |
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