Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783487323301740544
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
work_keys_str_mv AT evangelopoulosmichael biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT yazdiimank biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT acciardostefania biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT palombaroberto biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT giordanofederica biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT pastoanna biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT sushnithamanuela biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT martinezjonathano biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT basunupur biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT torresarmando biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT hmaidansarah biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT parodialessandro biomimeticcellularvectorsforenhancingdrugdeliverytothelungs
AT tasciottiennio biomimeticcellularvectorsforenhancingdrugdeliverytothelungs