A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors

Nanoparticle-based chemophotothermal therapy (CPT) is a promising treatment for multidrug resistant tumors. In this study, a drug nanococktail of DIR825@histone was developed by employing doxorubicin (DOX), NIR dye IR825 and human histones for interventional nucleus-targeted CPT of multidrug resista...

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Autores principales: Jianquan Guo, Dongsheng Tan, Chenmei Lou, Shiying Guo, Xing Jin, Haijing Qu, Lijia Jing, Sijin Li
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Lenguaje:EN
Publicado: KeAi Communications Co., Ltd. 2022
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Acceso en línea:https://doaj.org/article/cc4b0abac14d4b2c8edd406d42ac2b03
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spelling oai:doaj.org-article:cc4b0abac14d4b2c8edd406d42ac2b032021-11-10T04:30:36ZA tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors2452-199X10.1016/j.bioactmat.2021.07.018https://doaj.org/article/cc4b0abac14d4b2c8edd406d42ac2b032022-03-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2452199X21003492https://doaj.org/toc/2452-199XNanoparticle-based chemophotothermal therapy (CPT) is a promising treatment for multidrug resistant tumors. In this study, a drug nanococktail of DIR825@histone was developed by employing doxorubicin (DOX), NIR dye IR825 and human histones for interventional nucleus-targeted CPT of multidrug resistant tumors with an interventional laser. After localized intervention, DIR825@histone penetrated tumor tissues by transcytosis, efficiently entered tumor cells and targeted the cell nuclei. DIR825@histone also exhibited good photothermal performance and thermal-triggered drug release. Efficient multidrug resistant tumor inhibition was achieved by enhanced CPT sensitization and MDR reversion via nuclear targeting. Moreover, an interventional laser assisted DIR825@histone in inhibiting multidrug resistant tumors by promoting the sufficient delivery of laser energy inside the tumor while reducing skin injury. Therefore, DIR825@histone together with this interventional nucleus-targeted CPT strategy holds great promise for treating multidrug resistant tumors.Jianquan GuoDongsheng TanChenmei LouShiying GuoXing JinHaijing QuLijia JingSijin LiKeAi Communications Co., Ltd.articleHuman histonesChemotherapyPhotothermal therapyNuclear targetingLocalized interventionDrug resistant tumorMaterials of engineering and construction. Mechanics of materialsTA401-492Biology (General)QH301-705.5ENBioactive Materials, Vol 9, Iss , Pp 554-565 (2022)
institution DOAJ
collection DOAJ
language EN
topic Human histones
Chemotherapy
Photothermal therapy
Nuclear targeting
Localized intervention
Drug resistant tumor
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
spellingShingle Human histones
Chemotherapy
Photothermal therapy
Nuclear targeting
Localized intervention
Drug resistant tumor
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
Jianquan Guo
Dongsheng Tan
Chenmei Lou
Shiying Guo
Xing Jin
Haijing Qu
Lijia Jing
Sijin Li
A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
description Nanoparticle-based chemophotothermal therapy (CPT) is a promising treatment for multidrug resistant tumors. In this study, a drug nanococktail of DIR825@histone was developed by employing doxorubicin (DOX), NIR dye IR825 and human histones for interventional nucleus-targeted CPT of multidrug resistant tumors with an interventional laser. After localized intervention, DIR825@histone penetrated tumor tissues by transcytosis, efficiently entered tumor cells and targeted the cell nuclei. DIR825@histone also exhibited good photothermal performance and thermal-triggered drug release. Efficient multidrug resistant tumor inhibition was achieved by enhanced CPT sensitization and MDR reversion via nuclear targeting. Moreover, an interventional laser assisted DIR825@histone in inhibiting multidrug resistant tumors by promoting the sufficient delivery of laser energy inside the tumor while reducing skin injury. Therefore, DIR825@histone together with this interventional nucleus-targeted CPT strategy holds great promise for treating multidrug resistant tumors.
format article
author Jianquan Guo
Dongsheng Tan
Chenmei Lou
Shiying Guo
Xing Jin
Haijing Qu
Lijia Jing
Sijin Li
author_facet Jianquan Guo
Dongsheng Tan
Chenmei Lou
Shiying Guo
Xing Jin
Haijing Qu
Lijia Jing
Sijin Li
author_sort Jianquan Guo
title A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
title_short A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
title_full A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
title_fullStr A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
title_full_unstemmed A tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
title_sort tumor-penetrable drug nanococktail made from human histones for interventional nucleus-targeted chemophotothermal therapy of drug-resistant tumors
publisher KeAi Communications Co., Ltd.
publishDate 2022
url https://doaj.org/article/cc4b0abac14d4b2c8edd406d42ac2b03
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