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Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy
The efficacy of nano-mediated drug delivery has been impeded by multiple biological barriers such as the mononuclear phagocyte system (MPS), as well as vascular and interstitial barriers. To overcome the abovementioned obstacles, we report a nano-pathogenoid (NPN) system that can in situ hitchhike c...
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/PMC7048836/ https://www.ncbi.nlm.nih.gov/pubmed/32111847 http://dx.doi.org/10.1038/s41467-020-14963-0 |
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author | Li, Min Li, Shuya Zhou, Han Tang, Xinfeng Wu, Yi Jiang, Wei Tian, Zhigang Zhou, Xuechang Yang, Xianzhu Wang, Yucai |
author_facet | Li, Min Li, Shuya Zhou, Han Tang, Xinfeng Wu, Yi Jiang, Wei Tian, Zhigang Zhou, Xuechang Yang, Xianzhu Wang, Yucai |
author_sort | Li, Min |
collection | PubMed |
description | The efficacy of nano-mediated drug delivery has been impeded by multiple biological barriers such as the mononuclear phagocyte system (MPS), as well as vascular and interstitial barriers. To overcome the abovementioned obstacles, we report a nano-pathogenoid (NPN) system that can in situ hitchhike circulating neutrophils and supplement photothermal therapy (PTT). Cloaked with bacteria-secreted outer membrane vesicles inheriting pathogen-associated molecular patterns of native bacteria, NPNs are effectively recognized and internalized by neutrophils. The neutrophils migrate towards inflamed tumors, extravasate across the blood vessels, and penetrate through the tumors. Then NPNs are rapidly released from neutrophils in response to inflammatory stimuli and subsequently taken up by tumor cells to exert anticancer effects. Strikingly, due to the excellent targeting efficacy, cisplatin-loaded NPNs combined with PTT completely eradicate tumors in all treated mice. Such a nano-platform represents an efficient and generalizable strategy towards in situ cell hitchhiking as well as enhanced tumor targeted delivery. |
format | Online Article Text |
id | pubmed-7048836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70488362020-03-02 Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy Li, Min Li, Shuya Zhou, Han Tang, Xinfeng Wu, Yi Jiang, Wei Tian, Zhigang Zhou, Xuechang Yang, Xianzhu Wang, Yucai Nat Commun Article The efficacy of nano-mediated drug delivery has been impeded by multiple biological barriers such as the mononuclear phagocyte system (MPS), as well as vascular and interstitial barriers. To overcome the abovementioned obstacles, we report a nano-pathogenoid (NPN) system that can in situ hitchhike circulating neutrophils and supplement photothermal therapy (PTT). Cloaked with bacteria-secreted outer membrane vesicles inheriting pathogen-associated molecular patterns of native bacteria, NPNs are effectively recognized and internalized by neutrophils. The neutrophils migrate towards inflamed tumors, extravasate across the blood vessels, and penetrate through the tumors. Then NPNs are rapidly released from neutrophils in response to inflammatory stimuli and subsequently taken up by tumor cells to exert anticancer effects. Strikingly, due to the excellent targeting efficacy, cisplatin-loaded NPNs combined with PTT completely eradicate tumors in all treated mice. Such a nano-platform represents an efficient and generalizable strategy towards in situ cell hitchhiking as well as enhanced tumor targeted delivery. Nature Publishing Group UK 2020-02-28 /pmc/articles/PMC7048836/ /pubmed/32111847 http://dx.doi.org/10.1038/s41467-020-14963-0 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 Li, Min Li, Shuya Zhou, Han Tang, Xinfeng Wu, Yi Jiang, Wei Tian, Zhigang Zhou, Xuechang Yang, Xianzhu Wang, Yucai Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title | Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title_full | Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title_fullStr | Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title_full_unstemmed | Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title_short | Chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
title_sort | chemotaxis-driven delivery of nano-pathogenoids for complete eradication of tumors post-phototherapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048836/ https://www.ncbi.nlm.nih.gov/pubmed/32111847 http://dx.doi.org/10.1038/s41467-020-14963-0 |
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