A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer

Multienzyme-mimicking redox nanozymes, curated by defect engineering, in synergy with immunotherapy offer promising prospects for safe and efficient cancer therapy. However, the spatiotemporally precise immune response often gets challenged by off-target adverse effects and insufficient therapeutic...

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Main Authors: Jana, Deblin, He, Bing, Chen, Yun, Liu, Jiawei, Zhao, Yanli
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/170443
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1704432023-10-13T15:31:38Z A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer Jana, Deblin He, Bing Chen, Yun Liu, Jiawei Zhao, Yanli School of Chemistry, Chemical Engineering and Biotechnology Science::Chemistry Cancer Therapy Defect Engineering Multienzyme-mimicking redox nanozymes, curated by defect engineering, in synergy with immunotherapy offer promising prospects for safe and efficient cancer therapy. However, the spatiotemporally precise immune response often gets challenged by off-target adverse effects and insufficient therapeutic response. Herein, a tumor cell membrane coated redox nanozyme (CMO-R@4T1) is reported for combinational second near-infrared window (NIR-II) photothermal immunotherapy. CMO-R@4T1 consists of a Cu-doped MoOx (CMO) nanozyme as the core, which is cloaked with tumor-cell-derived fused membranes with immunostimulants immobilized in the membrane shell. In addition to the enhanced tumor accumulation, the nanozyme can cause oxidative damage to tumor cells by the production of reactive oxygen species and attenuation of the antioxidant mechanism. CMO-R@4T1 also mediates a photothermal effect under NIR-II photoirradiation to trigger tumor eradication and immunogenic cell death, where the liberated agonist elicits the immune activation. Such a controlled therapeutic paradigm potentiates systemic primary tumor ablation, inhibits cancer metastasis to distant tumor, and procures long-term immunological memory. Thereby, this study takes advantage of defect engineering to illustrate a generic strategy to prepare cell-membrane-camouflaged nanozymes for targeted photo-immunotherapy of cancer. Agency for Science, Technology and Research (A*STAR) National Research Foundation (NRF) Submitted/Accepted version This research was supported by the Singapore Agency for Science, Technology and Research (A*STAR) AME IRG grant (A20E5c0081) and the Singapore National Research Foundation Investigatorship (NRF-NRFI2018-03). 2023-09-12T05:28:57Z 2023-09-12T05:28:57Z 2022 Journal Article Jana, D., He, B., Chen, Y., Liu, J. & Zhao, Y. (2022). A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer. Advanced Materials. https://dx.doi.org/10.1002/adma.202206401 0935-9648 https://hdl.handle.net/10356/170443 10.1002/adma.202206401 36210733 2-s2.0-85141960519 en A20E5c0081 NRF-NRFI2018-03 Advanced Materials © 2022 Wiley-VCH GmbH. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1002/adma.202206401. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Chemistry
Cancer Therapy
Defect Engineering
spellingShingle Science::Chemistry
Cancer Therapy
Defect Engineering
Jana, Deblin
He, Bing
Chen, Yun
Liu, Jiawei
Zhao, Yanli
A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
description Multienzyme-mimicking redox nanozymes, curated by defect engineering, in synergy with immunotherapy offer promising prospects for safe and efficient cancer therapy. However, the spatiotemporally precise immune response often gets challenged by off-target adverse effects and insufficient therapeutic response. Herein, a tumor cell membrane coated redox nanozyme (CMO-R@4T1) is reported for combinational second near-infrared window (NIR-II) photothermal immunotherapy. CMO-R@4T1 consists of a Cu-doped MoOx (CMO) nanozyme as the core, which is cloaked with tumor-cell-derived fused membranes with immunostimulants immobilized in the membrane shell. In addition to the enhanced tumor accumulation, the nanozyme can cause oxidative damage to tumor cells by the production of reactive oxygen species and attenuation of the antioxidant mechanism. CMO-R@4T1 also mediates a photothermal effect under NIR-II photoirradiation to trigger tumor eradication and immunogenic cell death, where the liberated agonist elicits the immune activation. Such a controlled therapeutic paradigm potentiates systemic primary tumor ablation, inhibits cancer metastasis to distant tumor, and procures long-term immunological memory. Thereby, this study takes advantage of defect engineering to illustrate a generic strategy to prepare cell-membrane-camouflaged nanozymes for targeted photo-immunotherapy of cancer.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Jana, Deblin
He, Bing
Chen, Yun
Liu, Jiawei
Zhao, Yanli
format Article
author Jana, Deblin
He, Bing
Chen, Yun
Liu, Jiawei
Zhao, Yanli
author_sort Jana, Deblin
title A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
title_short A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
title_full A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
title_fullStr A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
title_full_unstemmed A defect-engineered nanozyme for targeted NIR-II photothermal immunotherapy of cancer
title_sort defect-engineered nanozyme for targeted nir-ii photothermal immunotherapy of cancer
publishDate 2023
url https://hdl.handle.net/10356/170443
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