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Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo
Surface charge plays a fundamental role in determining the fate of a nanoparticle, and any encapsulated contents, in vivo. Herein, we describe, and visualise in real time, light-triggered switching of liposome surface charge, from neutral to cationic, in situ and in vivo (embryonic zebrafish). Prior...
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/PMC7371701/ https://www.ncbi.nlm.nih.gov/pubmed/32686667 http://dx.doi.org/10.1038/s41467-020-17360-9 |
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author | Arias-Alpizar, Gabriela Kong, Li Vlieg, Redmar C. Rabe, Alexander Papadopoulou, Panagiota Meijer, Michael S. Bonnet, Sylvestre Vogel, Stefan van Noort, John Kros, Alexander Campbell, Frederick |
author_facet | Arias-Alpizar, Gabriela Kong, Li Vlieg, Redmar C. Rabe, Alexander Papadopoulou, Panagiota Meijer, Michael S. Bonnet, Sylvestre Vogel, Stefan van Noort, John Kros, Alexander Campbell, Frederick |
author_sort | Arias-Alpizar, Gabriela |
collection | PubMed |
description | Surface charge plays a fundamental role in determining the fate of a nanoparticle, and any encapsulated contents, in vivo. Herein, we describe, and visualise in real time, light-triggered switching of liposome surface charge, from neutral to cationic, in situ and in vivo (embryonic zebrafish). Prior to light activation, intravenously administered liposomes, composed of just two lipid reagents, freely circulate and successfully evade innate immune cells present in the fish. Upon in situ irradiation and surface charge switching, however, liposomes rapidly adsorb to, and are taken up by, endothelial cells and/or are phagocytosed by blood resident macrophages. Coupling complete external control of nanoparticle targeting together with the intracellular delivery of encapsulated (and membrane impermeable) cargos, these compositionally simple liposomes are proof that advanced nanoparticle function in vivo does not require increased design complexity but rather a thorough understanding of the fundamental nano-bio interactions involved. |
format | Online Article Text |
id | pubmed-7371701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73717012020-07-22 Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo Arias-Alpizar, Gabriela Kong, Li Vlieg, Redmar C. Rabe, Alexander Papadopoulou, Panagiota Meijer, Michael S. Bonnet, Sylvestre Vogel, Stefan van Noort, John Kros, Alexander Campbell, Frederick Nat Commun Article Surface charge plays a fundamental role in determining the fate of a nanoparticle, and any encapsulated contents, in vivo. Herein, we describe, and visualise in real time, light-triggered switching of liposome surface charge, from neutral to cationic, in situ and in vivo (embryonic zebrafish). Prior to light activation, intravenously administered liposomes, composed of just two lipid reagents, freely circulate and successfully evade innate immune cells present in the fish. Upon in situ irradiation and surface charge switching, however, liposomes rapidly adsorb to, and are taken up by, endothelial cells and/or are phagocytosed by blood resident macrophages. Coupling complete external control of nanoparticle targeting together with the intracellular delivery of encapsulated (and membrane impermeable) cargos, these compositionally simple liposomes are proof that advanced nanoparticle function in vivo does not require increased design complexity but rather a thorough understanding of the fundamental nano-bio interactions involved. Nature Publishing Group UK 2020-07-20 /pmc/articles/PMC7371701/ /pubmed/32686667 http://dx.doi.org/10.1038/s41467-020-17360-9 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 Arias-Alpizar, Gabriela Kong, Li Vlieg, Redmar C. Rabe, Alexander Papadopoulou, Panagiota Meijer, Michael S. Bonnet, Sylvestre Vogel, Stefan van Noort, John Kros, Alexander Campbell, Frederick Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title | Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title_full | Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title_fullStr | Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title_full_unstemmed | Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title_short | Light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
title_sort | light-triggered switching of liposome surface charge directs delivery of membrane impermeable payloads in vivo |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7371701/ https://www.ncbi.nlm.nih.gov/pubmed/32686667 http://dx.doi.org/10.1038/s41467-020-17360-9 |
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