A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy

Detalhes bibliográficos
Autor(a) principal: Chen, Xu
Data de Publicação: 2024
Outros Autores: Mendes, Bárbara B., Zhuang, Yunhui, Conniot, João, Mercado Argandona, Sergio, Melle, Francesca, Sousa, Diana P., Perl, David, Chivu, Alexandru, Patra, Hirak K., Shepard, William, Conde, João, Fairen-Jimenez, David
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/162426
Resumo: Funding Information: This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 Research and Innovation Programme (NanoMOFdeli), ERC-2016-COG 726380, and the EPSRC (EP/S009000/1). This work was supported by the FCT PhD Scholarship (2020.06638.BD, Diana P. Sousa) and the European Research Council Starting Grant ERC-StG-2019-848325 (2019–2024, João Conde, João Conniot, and Bárbara Mendes). The Talos F200X G2 TEM was supported through an EPSRC Underpinning Multi-User Equipment Grant (EP/P030467/1). The authors thank the staff of PROXIMA-2A (Soleil Synchrotron, France) for assistance and acknowledge the beamtime under the in-house research proposal 99220022 and standard proposal 20220874. They also thank Dr. Karin Mueller and Dr. Filomena Gallo from the Cambridge Advanced Imaging Centre, Department of Physiology and Neuroscience, University of Cambridge, for assistance in performing TEM imaging on the stained cells. The authors thank Histopathology Unit at Gulbenkian Science Institute for quantitative pathology evaluation and Histological Facility at Nova Medical School for technical assistance in sample preparation. TOC and a,b were created with BioRender.com. Publisher Copyright: © 2024 The Authors. Published by American Chemical Society
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spelling A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic TherapyCatalysisChemistry(all)BiochemistryColloid and Surface ChemistrySDG 3 - Good Health and Well-beingFunding Information: This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 Research and Innovation Programme (NanoMOFdeli), ERC-2016-COG 726380, and the EPSRC (EP/S009000/1). This work was supported by the FCT PhD Scholarship (2020.06638.BD, Diana P. Sousa) and the European Research Council Starting Grant ERC-StG-2019-848325 (2019–2024, João Conde, João Conniot, and Bárbara Mendes). The Talos F200X G2 TEM was supported through an EPSRC Underpinning Multi-User Equipment Grant (EP/P030467/1). The authors thank the staff of PROXIMA-2A (Soleil Synchrotron, France) for assistance and acknowledge the beamtime under the in-house research proposal 99220022 and standard proposal 20220874. They also thank Dr. Karin Mueller and Dr. Filomena Gallo from the Cambridge Advanced Imaging Centre, Department of Physiology and Neuroscience, University of Cambridge, for assistance in performing TEM imaging on the stained cells. The authors thank Histopathology Unit at Gulbenkian Science Institute for quantitative pathology evaluation and Histological Facility at Nova Medical School for technical assistance in sample preparation. TOC and a,b were created with BioRender.com. Publisher Copyright: © 2024 The Authors. Published by American Chemical SocietyPhotodynamic therapy (PDT), an emergent noninvasive cancer treatment, is largely dependent on the presence of efficient photosensitizers (PSs) and a sufficient oxygen supply. However, the therapeutic efficacy of PSs is greatly compromised by poor solubility, aggregation tendency, and oxygen depletion within solid tumors during PDT in hypoxic microenvironments. Despite the potential of PS-based metal-organic frameworks (MOFs), addressing hypoxia remains challenging. Boron dipyrromethene (BODIPY) chromophores, with excellent photostability, have exhibited great potential in PDT and bioimaging. However, their practical application suffers from limited chemical stability under harsh MOF synthesis conditions. Herein, we report the synthesis of the first example of a Zr-based MOF, namely, 69-L2, exclusively constructed from the BODIPY-derived ligands via a single-crystal to single-crystal post-synthetic exchange, where a direct solvothermal method is not applicable. To increase the PDT performance in hypoxia, we modify 69-L2 with fluorinated phosphate-functionalized methoxy poly(ethylene glycol). The resulting 69-L2@F is an oxygen carrier, enabling tumor oxygenation and simultaneously acting as a PS for reactive oxygen species (ROS) generation under LED irradiation. We demonstrate that 69-L2@F has an enhanced PDT effect in triple-negative breast cancer MDA-MB-231 cells under both normoxia and hypoxia. Following positive results, we evaluated the in vivo activity of 69-L2@F with a hydrogel, enabling local therapy in a triple-negative breast cancer mice model and achieving exceptional antitumor efficacy in only 2 days. We envision BODIPY-based Zr-MOFs to provide a solution for hypoxia relief and maximize efficacy during in vivo PDT, offering new insights into the design of promising MOF-based PSs for hypoxic tumors.NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)Centre for Toxicogenomics and Human Health (ToxOmics)RUNChen, XuMendes, Bárbara B.Zhuang, YunhuiConniot, JoãoMercado Argandona, SergioMelle, FrancescaSousa, Diana P.Perl, DavidChivu, AlexandruPatra, Hirak K.Shepard, WilliamConde, JoãoFairen-Jimenez, David2024-01-17T22:37:33Z2024-012024-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/162426eng0002-7863PURE: 81713768https://doi.org/10.1021/jacs.3c12416info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T05:45:21Zoai:run.unl.pt:10362/162426Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:58:54.292491Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
title A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
spellingShingle A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
Chen, Xu
Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry
SDG 3 - Good Health and Well-being
title_short A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
title_full A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
title_fullStr A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
title_full_unstemmed A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
title_sort A Fluorinated BODIPY-Based Zirconium Metal-Organic Framework for In Vivo Enhanced Photodynamic Therapy
author Chen, Xu
author_facet Chen, Xu
Mendes, Bárbara B.
Zhuang, Yunhui
Conniot, João
Mercado Argandona, Sergio
Melle, Francesca
Sousa, Diana P.
Perl, David
Chivu, Alexandru
Patra, Hirak K.
Shepard, William
Conde, João
Fairen-Jimenez, David
author_role author
author2 Mendes, Bárbara B.
Zhuang, Yunhui
Conniot, João
Mercado Argandona, Sergio
Melle, Francesca
Sousa, Diana P.
Perl, David
Chivu, Alexandru
Patra, Hirak K.
Shepard, William
Conde, João
Fairen-Jimenez, David
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv NOVA Medical School|Faculdade de Ciências Médicas (NMS|FCM)
Centre for Toxicogenomics and Human Health (ToxOmics)
RUN
dc.contributor.author.fl_str_mv Chen, Xu
Mendes, Bárbara B.
Zhuang, Yunhui
Conniot, João
Mercado Argandona, Sergio
Melle, Francesca
Sousa, Diana P.
Perl, David
Chivu, Alexandru
Patra, Hirak K.
Shepard, William
Conde, João
Fairen-Jimenez, David
dc.subject.por.fl_str_mv Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry
SDG 3 - Good Health and Well-being
topic Catalysis
Chemistry(all)
Biochemistry
Colloid and Surface Chemistry
SDG 3 - Good Health and Well-being
description Funding Information: This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 Research and Innovation Programme (NanoMOFdeli), ERC-2016-COG 726380, and the EPSRC (EP/S009000/1). This work was supported by the FCT PhD Scholarship (2020.06638.BD, Diana P. Sousa) and the European Research Council Starting Grant ERC-StG-2019-848325 (2019–2024, João Conde, João Conniot, and Bárbara Mendes). The Talos F200X G2 TEM was supported through an EPSRC Underpinning Multi-User Equipment Grant (EP/P030467/1). The authors thank the staff of PROXIMA-2A (Soleil Synchrotron, France) for assistance and acknowledge the beamtime under the in-house research proposal 99220022 and standard proposal 20220874. They also thank Dr. Karin Mueller and Dr. Filomena Gallo from the Cambridge Advanced Imaging Centre, Department of Physiology and Neuroscience, University of Cambridge, for assistance in performing TEM imaging on the stained cells. The authors thank Histopathology Unit at Gulbenkian Science Institute for quantitative pathology evaluation and Histological Facility at Nova Medical School for technical assistance in sample preparation. TOC and a,b were created with BioRender.com. Publisher Copyright: © 2024 The Authors. Published by American Chemical Society
publishDate 2024
dc.date.none.fl_str_mv 2024-01-17T22:37:33Z
2024-01
2024-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10362/162426
url http://hdl.handle.net/10362/162426
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0002-7863
PURE: 81713768
https://doi.org/10.1021/jacs.3c12416
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eu_rights_str_mv openAccess
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