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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...

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Autores principales: Li, Min, Li, Shuya, Zhou, Han, Tang, Xinfeng, Wu, Yi, Jiang, Wei, Tian, Zhigang, Zhou, Xuechang, Yang, Xianzhu, Wang, Yucai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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.
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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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