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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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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. |
format | Online Article Text |
id | pubmed-10667824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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