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Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation
Local delivery of biotherapeutics to the lung holds great promise for treatment of lung diseases, but development of physically stable, biologically active dry powder formulations of large molecules for inhalation has remained a challenge. Here, spray drying was used to manufacture a dry powder pulm...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408070/ https://www.ncbi.nlm.nih.gov/pubmed/34467438 http://dx.doi.org/10.1208/s12249-021-02095-7 |
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author | Shepard, Kimberly B. Vodak, David T. Kuehl, Philip J. Revelli, David Zhou, Yue Pluntze, Amanda M. Adam, Molly S. Oddo, Julia C. Switala, Lauren Cape, Jonathan L. Baumann, John M. Banks, Michael |
author_facet | Shepard, Kimberly B. Vodak, David T. Kuehl, Philip J. Revelli, David Zhou, Yue Pluntze, Amanda M. Adam, Molly S. Oddo, Julia C. Switala, Lauren Cape, Jonathan L. Baumann, John M. Banks, Michael |
author_sort | Shepard, Kimberly B. |
collection | PubMed |
description | Local delivery of biotherapeutics to the lung holds great promise for treatment of lung diseases, but development of physically stable, biologically active dry powder formulations of large molecules for inhalation has remained a challenge. Here, spray drying was used to manufacture a dry powder pulmonary formulation of bevacizumab, a monoclonal antibody approved to treat non-small cell lung cancer (NSCLC) by intravenous infusion. By reformulating bevacizumab for local delivery, reduced side effects, lower doses, and improved patient compliance are possible. The formulation had aerosol properties suitable for delivery to the deep lung, as well as good physical stability at ambient temperature for at least 6 months. Bevacizumab’s anti-VEGF bioactivity was not impacted by the manufacturing process. The formulation was efficacious in an in vivo rat model for NSCLC at a 10-fold decrease in dose relative to the intravenous control. |
format | Online Article Text |
id | pubmed-8408070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-84080702021-09-09 Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation Shepard, Kimberly B. Vodak, David T. Kuehl, Philip J. Revelli, David Zhou, Yue Pluntze, Amanda M. Adam, Molly S. Oddo, Julia C. Switala, Lauren Cape, Jonathan L. Baumann, John M. Banks, Michael AAPS PharmSciTech Research Article Local delivery of biotherapeutics to the lung holds great promise for treatment of lung diseases, but development of physically stable, biologically active dry powder formulations of large molecules for inhalation has remained a challenge. Here, spray drying was used to manufacture a dry powder pulmonary formulation of bevacizumab, a monoclonal antibody approved to treat non-small cell lung cancer (NSCLC) by intravenous infusion. By reformulating bevacizumab for local delivery, reduced side effects, lower doses, and improved patient compliance are possible. The formulation had aerosol properties suitable for delivery to the deep lung, as well as good physical stability at ambient temperature for at least 6 months. Bevacizumab’s anti-VEGF bioactivity was not impacted by the manufacturing process. The formulation was efficacious in an in vivo rat model for NSCLC at a 10-fold decrease in dose relative to the intravenous control. Springer International Publishing 2021-08-31 /pmc/articles/PMC8408070/ /pubmed/34467438 http://dx.doi.org/10.1208/s12249-021-02095-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Shepard, Kimberly B. Vodak, David T. Kuehl, Philip J. Revelli, David Zhou, Yue Pluntze, Amanda M. Adam, Molly S. Oddo, Julia C. Switala, Lauren Cape, Jonathan L. Baumann, John M. Banks, Michael Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title | Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title_full | Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title_fullStr | Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title_full_unstemmed | Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title_short | Local Treatment of Non-small Cell Lung Cancer with a Spray-Dried Bevacizumab Formulation |
title_sort | local treatment of non-small cell lung cancer with a spray-dried bevacizumab formulation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8408070/ https://www.ncbi.nlm.nih.gov/pubmed/34467438 http://dx.doi.org/10.1208/s12249-021-02095-7 |
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