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Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy

Metal–organic framework (MOF)‐based drug delivery systems have demonstrated values in oncotherapy. Current research endeavors are centralized on the functionality enrichment of featured MOF materials with designed versatility for synergistic multimodal treatments. Here, inspired by the multifarious...

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Autores principales: Zhang, Qingfei, Kuang, Gaizhen, Wang, Hanbing, Zhao, Yuanjin, Wei, Jia, Shang, Luoran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667824/
https://www.ncbi.nlm.nih.gov/pubmed/37852943
http://dx.doi.org/10.1002/advs.202303818
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author Zhang, Qingfei
Kuang, Gaizhen
Wang, Hanbing
Zhao, Yuanjin
Wei, Jia
Shang, Luoran
author_facet Zhang, Qingfei
Kuang, Gaizhen
Wang, Hanbing
Zhao, Yuanjin
Wei, Jia
Shang, Luoran
author_sort Zhang, Qingfei
collection PubMed
description Metal–organic framework (MOF)‐based drug delivery systems have demonstrated values in oncotherapy. Current research endeavors are centralized on the functionality enrichment of featured MOF materials with designed versatility for synergistic multimodal treatments. Here, inspired by the multifarious biological functions including ferroptosis pattern, porphyrins, and cancer cell membrane (CCM) camouflage technique, novel multi‐biomimetic MOF nanocarriers from microfluidics are prepared. The Fe(3+), meso‐tetra(4‐carboxyphenyl)porphine and oxaliplatin prodrug are incorporated into one MOF nano‐system (named FeTPt), which is further cloaked by CCM to obtain a “Trojan Horse”‐like vehicle (FeTPt@CCM). Owing to the functionalization with CCM, FeTPt@CCM can target and accumulate at the tumor site via homologous binding. After being internalized by cancer cells, FeTPt@CCM can be activated by a Fenton‐like reaction as well as a redox reaction between Fe(3+) and glutathione and hydrogen peroxide to generate hydroxyl radical and oxygen. Thus, the nano‐platform effectively initiates ferroptosis and improves photodynamic therapy performance. Along with the Pt‐drug chemotherapy, the nano‐platform exhibits synergistic multimodal actions for inhibiting cancer cell proliferation in vitro and suppressing tumor growth in vivo. These features indicate that such a versatile biomimetic MOF delivery system from microfluidics has great potential for synergistic cancer treatment.
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spelling pubmed-106678242023-10-18 Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy Zhang, Qingfei Kuang, Gaizhen Wang, Hanbing Zhao, Yuanjin Wei, Jia Shang, Luoran Adv Sci (Weinh) Research Articles Metal–organic framework (MOF)‐based drug delivery systems have demonstrated values in oncotherapy. Current research endeavors are centralized on the functionality enrichment of featured MOF materials with designed versatility for synergistic multimodal treatments. Here, inspired by the multifarious biological functions including ferroptosis pattern, porphyrins, and cancer cell membrane (CCM) camouflage technique, novel multi‐biomimetic MOF nanocarriers from microfluidics are prepared. The Fe(3+), meso‐tetra(4‐carboxyphenyl)porphine and oxaliplatin prodrug are incorporated into one MOF nano‐system (named FeTPt), which is further cloaked by CCM to obtain a “Trojan Horse”‐like vehicle (FeTPt@CCM). Owing to the functionalization with CCM, FeTPt@CCM can target and accumulate at the tumor site via homologous binding. After being internalized by cancer cells, FeTPt@CCM can be activated by a Fenton‐like reaction as well as a redox reaction between Fe(3+) and glutathione and hydrogen peroxide to generate hydroxyl radical and oxygen. Thus, the nano‐platform effectively initiates ferroptosis and improves photodynamic therapy performance. Along with the Pt‐drug chemotherapy, the nano‐platform exhibits synergistic multimodal actions for inhibiting cancer cell proliferation in vitro and suppressing tumor growth in vivo. These features indicate that such a versatile biomimetic MOF delivery system from microfluidics has great potential for synergistic cancer treatment. John Wiley and Sons Inc. 2023-10-18 /pmc/articles/PMC10667824/ /pubmed/37852943 http://dx.doi.org/10.1002/advs.202303818 Text en © 2023 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Qingfei
Kuang, Gaizhen
Wang, Hanbing
Zhao, Yuanjin
Wei, Jia
Shang, Luoran
Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title_full Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title_fullStr Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title_full_unstemmed Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title_short Multi‐Bioinspired MOF Delivery Systems from Microfluidics for Tumor Multimodal Therapy
title_sort multi‐bioinspired mof delivery systems from microfluidics for tumor multimodal therapy
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667824/
https://www.ncbi.nlm.nih.gov/pubmed/37852943
http://dx.doi.org/10.1002/advs.202303818
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