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Biomimetic cellular vectors for enhancing drug delivery to the lungs
Despite recent advances in drug delivery, the targeted treatment of unhealthy cells or tissues continues to remain a priority. In cancer (much like other pathologies), delivery vectors are designed to exploit physical and biological features of unhealthy tissues that are not always homogenous across...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957529/ https://www.ncbi.nlm.nih.gov/pubmed/31932600 http://dx.doi.org/10.1038/s41598-019-55909-x |
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author | Evangelopoulos, Michael Yazdi, Iman K. Acciardo, Stefania Palomba, Roberto Giordano, Federica Pasto, Anna Sushnitha, Manuela Martinez, Jonathan O. Basu, Nupur Torres, Armando Hmaidan, Sarah Parodi, Alessandro Tasciotti, Ennio |
author_facet | Evangelopoulos, Michael Yazdi, Iman K. Acciardo, Stefania Palomba, Roberto Giordano, Federica Pasto, Anna Sushnitha, Manuela Martinez, Jonathan O. Basu, Nupur Torres, Armando Hmaidan, Sarah Parodi, Alessandro Tasciotti, Ennio |
author_sort | Evangelopoulos, Michael |
collection | PubMed |
description | Despite recent advances in drug delivery, the targeted treatment of unhealthy cells or tissues continues to remain a priority. In cancer (much like other pathologies), delivery vectors are designed to exploit physical and biological features of unhealthy tissues that are not always homogenous across the disease. In some cases, shifting the target from unhealthy tissues to the whole organ can represent an advantage. Specifically, the natural organ-specific retention of nanotherapeutics following intravenous administration as seen in the lung, liver, and spleen can be strategically exploited to enhance drug delivery. Herein, we outline the development of a cell-based delivery system using macrophages as a delivery vehicle. When loaded with a chemotherapeutic payload (i.e., doxorubicin), these cellular vectors (CELVEC) were shown to provide continued release within the lung. This study provides proof-of-concept evidence of an alternative class of biomimetic delivery vectors that capitalize on cell size to provide therapeutic advantages for pulmonary treatments. |
format | Online Article Text |
id | pubmed-6957529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69575292020-01-16 Biomimetic cellular vectors for enhancing drug delivery to the lungs Evangelopoulos, Michael Yazdi, Iman K. Acciardo, Stefania Palomba, Roberto Giordano, Federica Pasto, Anna Sushnitha, Manuela Martinez, Jonathan O. Basu, Nupur Torres, Armando Hmaidan, Sarah Parodi, Alessandro Tasciotti, Ennio Sci Rep Article Despite recent advances in drug delivery, the targeted treatment of unhealthy cells or tissues continues to remain a priority. In cancer (much like other pathologies), delivery vectors are designed to exploit physical and biological features of unhealthy tissues that are not always homogenous across the disease. In some cases, shifting the target from unhealthy tissues to the whole organ can represent an advantage. Specifically, the natural organ-specific retention of nanotherapeutics following intravenous administration as seen in the lung, liver, and spleen can be strategically exploited to enhance drug delivery. Herein, we outline the development of a cell-based delivery system using macrophages as a delivery vehicle. When loaded with a chemotherapeutic payload (i.e., doxorubicin), these cellular vectors (CELVEC) were shown to provide continued release within the lung. This study provides proof-of-concept evidence of an alternative class of biomimetic delivery vectors that capitalize on cell size to provide therapeutic advantages for pulmonary treatments. Nature Publishing Group UK 2020-01-13 /pmc/articles/PMC6957529/ /pubmed/31932600 http://dx.doi.org/10.1038/s41598-019-55909-x Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Evangelopoulos, Michael Yazdi, Iman K. Acciardo, Stefania Palomba, Roberto Giordano, Federica Pasto, Anna Sushnitha, Manuela Martinez, Jonathan O. Basu, Nupur Torres, Armando Hmaidan, Sarah Parodi, Alessandro Tasciotti, Ennio Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title | Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title_full | Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title_fullStr | Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title_full_unstemmed | Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title_short | Biomimetic cellular vectors for enhancing drug delivery to the lungs |
title_sort | biomimetic cellular vectors for enhancing drug delivery to the lungs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957529/ https://www.ncbi.nlm.nih.gov/pubmed/31932600 http://dx.doi.org/10.1038/s41598-019-55909-x |
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