Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy

Sonodynamic therapy can trigger immunogenic cell death to augment immunotherapy, benefiting from its superior spatiotemporal selectivity and non-invasiveness. However, the practical applications of sonosensitizers are hindered by their low efficacy in killing cancer cells and activating immune respo...

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Main Authors: Cheng, Yu, Zhong, Wenbin, Chen, Yun, Tan, Brynne Shu Ni, Zhao, Yue, Guo, Jingjing, Ma, Mengmeng, Zhao, Yanli
Other Authors: School of Chemistry, Chemical Engineering and Biotechnology
Format: Article
Language:English
Published: 2024
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Online Access:https://hdl.handle.net/10356/181216
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1812162024-11-18T02:41:01Z Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy Cheng, Yu Zhong, Wenbin Chen, Yun Tan, Brynne Shu Ni Zhao, Yue Guo, Jingjing Ma, Mengmeng Zhao, Yanli School of Chemistry, Chemical Engineering and Biotechnology Engineering Bimetal-biligand frameworks Cancer treatment Sonodynamic therapy can trigger immunogenic cell death to augment immunotherapy, benefiting from its superior spatiotemporal selectivity and non-invasiveness. However, the practical applications of sonosensitizers are hindered by their low efficacy in killing cancer cells and activating immune responses. Here, two US Food and Drug Administration-approved drug ligands (ferricyanide and nitroprusside) and two types of metals (copper/iron) are selected to construct a bimetal-biligand framework (Cu[PBA-NO]). Through elaborate regulation of multiple metal/ligand coordination, the systemically administered Cu[PBA-NO] nanoagent shows sono-catalytic and NO release ability under ultrasound irradiation, which can be used for effective sono-immunotherapy. Moreover, Cu[PBA-NO] can downregulate intracellular glutathione levels that would destroy intracellular redox homeostasis and facilitate reactive oxygen species accumulation. The released tumor-associated antigens subsequently facilitate dendritic cell maturation within the tumor-draining lymph node, effectively initiating a T cell-mediated immune response and thereby bolstering the capacity to identify and combat cancer cells. This study paves a new avenue for the efficient cancer sono-immunotherapy. The authors acknowledge the support from the National Research Foundation Singapore under Its Competitive Research Programme (NRF-CRP26-2021-0002). 2024-11-18T02:41:01Z 2024-11-18T02:41:01Z 2024 Journal Article Cheng, Y., Zhong, W., Chen, Y., Tan, B. S. N., Zhao, Y., Guo, J., Ma, M. & Zhao, Y. (2024). Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy. Advanced Materials, 36(45), e2408242-. https://dx.doi.org/10.1002/adma.202408242 0935-9648 https://hdl.handle.net/10356/181216 10.1002/adma.202408242 39225414 2-s2.0-85202959029 45 36 e2408242 en NRF-CRP26-2021-0002 Advanced Materials © 2024 Wiley-VCH GmbH. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering
Bimetal-biligand frameworks
Cancer treatment
spellingShingle Engineering
Bimetal-biligand frameworks
Cancer treatment
Cheng, Yu
Zhong, Wenbin
Chen, Yun
Tan, Brynne Shu Ni
Zhao, Yue
Guo, Jingjing
Ma, Mengmeng
Zhao, Yanli
Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
description Sonodynamic therapy can trigger immunogenic cell death to augment immunotherapy, benefiting from its superior spatiotemporal selectivity and non-invasiveness. However, the practical applications of sonosensitizers are hindered by their low efficacy in killing cancer cells and activating immune responses. Here, two US Food and Drug Administration-approved drug ligands (ferricyanide and nitroprusside) and two types of metals (copper/iron) are selected to construct a bimetal-biligand framework (Cu[PBA-NO]). Through elaborate regulation of multiple metal/ligand coordination, the systemically administered Cu[PBA-NO] nanoagent shows sono-catalytic and NO release ability under ultrasound irradiation, which can be used for effective sono-immunotherapy. Moreover, Cu[PBA-NO] can downregulate intracellular glutathione levels that would destroy intracellular redox homeostasis and facilitate reactive oxygen species accumulation. The released tumor-associated antigens subsequently facilitate dendritic cell maturation within the tumor-draining lymph node, effectively initiating a T cell-mediated immune response and thereby bolstering the capacity to identify and combat cancer cells. This study paves a new avenue for the efficient cancer sono-immunotherapy.
author2 School of Chemistry, Chemical Engineering and Biotechnology
author_facet School of Chemistry, Chemical Engineering and Biotechnology
Cheng, Yu
Zhong, Wenbin
Chen, Yun
Tan, Brynne Shu Ni
Zhao, Yue
Guo, Jingjing
Ma, Mengmeng
Zhao, Yanli
format Article
author Cheng, Yu
Zhong, Wenbin
Chen, Yun
Tan, Brynne Shu Ni
Zhao, Yue
Guo, Jingjing
Ma, Mengmeng
Zhao, Yanli
author_sort Cheng, Yu
title Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
title_short Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
title_full Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
title_fullStr Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
title_full_unstemmed Bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
title_sort bimetal-biligand frameworks for spatiotemporal nitric oxide-enhanced sono-immunotherapy
publishDate 2024
url https://hdl.handle.net/10356/181216
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