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Hyperthermia-triggered biomimetic bubble nanomachines

Nanoparticle-based drug delivery systems have gained much attention in the treatment of various malignant tumors during the past decades. However, limited tumor penetration of nanodrugs remains a significant hurdle for effective tumor therapy due to the existing biological barriers of tumoral microe...

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Autores principales: Gao, Junbin, Qin, Hanfeng, Wang, Fei, Liu, Lu, Tian, Hao, Wang, Hong, Wang, Shuanghu, Ou, Juanfeng, Ye, Yicheng, Peng, Fei, Tu, Yingfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421929/
https://www.ncbi.nlm.nih.gov/pubmed/37567901
http://dx.doi.org/10.1038/s41467-023-40474-9
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author Gao, Junbin
Qin, Hanfeng
Wang, Fei
Liu, Lu
Tian, Hao
Wang, Hong
Wang, Shuanghu
Ou, Juanfeng
Ye, Yicheng
Peng, Fei
Tu, Yingfeng
author_facet Gao, Junbin
Qin, Hanfeng
Wang, Fei
Liu, Lu
Tian, Hao
Wang, Hong
Wang, Shuanghu
Ou, Juanfeng
Ye, Yicheng
Peng, Fei
Tu, Yingfeng
author_sort Gao, Junbin
collection PubMed
description Nanoparticle-based drug delivery systems have gained much attention in the treatment of various malignant tumors during the past decades. However, limited tumor penetration of nanodrugs remains a significant hurdle for effective tumor therapy due to the existing biological barriers of tumoral microenvironment. Inspired by bubble machines, here we report the successful fabrication of biomimetic nanodevices capable of in-situ secreting cell-membrane-derived nanovesicles with smaller sizes under near infrared (NIR) laser irradiation for synergistic photothermal/photodynamic therapy. Porous Au nanocages (AuNC) are loaded with phase transitable perfluorohexane (PFO) and hemoglobin (Hb), followed by oxygen pre-saturation and indocyanine green (ICG) anchored 4T1 tumor cell membrane camouflage. Upon slight laser treatment, the loaded PFO undergoes phase transition due to surface plasmon resonance effect produced by AuNC framework, thus inducing the budding of outer cell membrane coating into small-scale nanovesicles based on the pore size of AuNC. Therefore, the hyperthermia-triggered generation of nanovesicles with smaller size, sufficient oxygen supply and anchored ICG results in enhanced tumor penetration for further self-sufficient oxygen-augmented photodynamic therapy and photothermal therapy. The as-developed biomimetic bubble nanomachines with temperature responsiveness show great promise as a potential nanoplatform for cancer treatment.
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spelling pubmed-104219292023-08-13 Hyperthermia-triggered biomimetic bubble nanomachines Gao, Junbin Qin, Hanfeng Wang, Fei Liu, Lu Tian, Hao Wang, Hong Wang, Shuanghu Ou, Juanfeng Ye, Yicheng Peng, Fei Tu, Yingfeng Nat Commun Article Nanoparticle-based drug delivery systems have gained much attention in the treatment of various malignant tumors during the past decades. However, limited tumor penetration of nanodrugs remains a significant hurdle for effective tumor therapy due to the existing biological barriers of tumoral microenvironment. Inspired by bubble machines, here we report the successful fabrication of biomimetic nanodevices capable of in-situ secreting cell-membrane-derived nanovesicles with smaller sizes under near infrared (NIR) laser irradiation for synergistic photothermal/photodynamic therapy. Porous Au nanocages (AuNC) are loaded with phase transitable perfluorohexane (PFO) and hemoglobin (Hb), followed by oxygen pre-saturation and indocyanine green (ICG) anchored 4T1 tumor cell membrane camouflage. Upon slight laser treatment, the loaded PFO undergoes phase transition due to surface plasmon resonance effect produced by AuNC framework, thus inducing the budding of outer cell membrane coating into small-scale nanovesicles based on the pore size of AuNC. Therefore, the hyperthermia-triggered generation of nanovesicles with smaller size, sufficient oxygen supply and anchored ICG results in enhanced tumor penetration for further self-sufficient oxygen-augmented photodynamic therapy and photothermal therapy. The as-developed biomimetic bubble nanomachines with temperature responsiveness show great promise as a potential nanoplatform for cancer treatment. Nature Publishing Group UK 2023-08-11 /pmc/articles/PMC10421929/ /pubmed/37567901 http://dx.doi.org/10.1038/s41467-023-40474-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gao, Junbin
Qin, Hanfeng
Wang, Fei
Liu, Lu
Tian, Hao
Wang, Hong
Wang, Shuanghu
Ou, Juanfeng
Ye, Yicheng
Peng, Fei
Tu, Yingfeng
Hyperthermia-triggered biomimetic bubble nanomachines
title Hyperthermia-triggered biomimetic bubble nanomachines
title_full Hyperthermia-triggered biomimetic bubble nanomachines
title_fullStr Hyperthermia-triggered biomimetic bubble nanomachines
title_full_unstemmed Hyperthermia-triggered biomimetic bubble nanomachines
title_short Hyperthermia-triggered biomimetic bubble nanomachines
title_sort hyperthermia-triggered biomimetic bubble nanomachines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421929/
https://www.ncbi.nlm.nih.gov/pubmed/37567901
http://dx.doi.org/10.1038/s41467-023-40474-9
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