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Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite
Cu-BTC framework has received a considerable attention in recent years as a drug carrier candidate for cancer treatment due to its unique structural properties and promising biocompatibility. However, its intrinsic deficiency for medical imaging potentially limits its bioapplications; To address thi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114589/ https://www.ncbi.nlm.nih.gov/pubmed/37091862 http://dx.doi.org/10.3389/fmolb.2023.1071376 |
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author | Gharehdaghi, Zahra Naghib, Seyed Morteza Rahimi, Rahmatollah Bakhshi, Atin Kefayat, Amirhosein shamaeizadeh, Armin Molaabasi, Fatemeh |
author_facet | Gharehdaghi, Zahra Naghib, Seyed Morteza Rahimi, Rahmatollah Bakhshi, Atin Kefayat, Amirhosein shamaeizadeh, Armin Molaabasi, Fatemeh |
author_sort | Gharehdaghi, Zahra |
collection | PubMed |
description | Cu-BTC framework has received a considerable attention in recent years as a drug carrier candidate for cancer treatment due to its unique structural properties and promising biocompatibility. However, its intrinsic deficiency for medical imaging potentially limits its bioapplications; To address this subject, a magnetic nano/microscale MOF has been successfully fabricated by introducing Fe(3)O(4) nanoparticles as an imaging agent into the porous isoreticular MOF [Cu(3)(BTC)(2)] as a drug carrier. The synthesized magnetic MOFs exhibits a high loading capacity (40.5%) toward the model anticancer DOX with an excellent pH-responsive drug release. The proposed nanocomposite not only possesses large surface area, high magnetic response, large mesopore volume, high transverse relaxivity (r (2)) and good stability but also exhibits superior biocompatibility, specific tumor cellular uptake, and significant cancer cell viability inhibitory effect without any targeting agent. It is expected that the synthesized magnetic nano/microcomposite may be used for clinical purposes and can also serve as a platform for photoactive antibacterial therapy ae well as pH/GSH/photo-triple-responsive nanocarrier. |
format | Online Article Text |
id | pubmed-10114589 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101145892023-04-20 Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite Gharehdaghi, Zahra Naghib, Seyed Morteza Rahimi, Rahmatollah Bakhshi, Atin Kefayat, Amirhosein shamaeizadeh, Armin Molaabasi, Fatemeh Front Mol Biosci Molecular Biosciences Cu-BTC framework has received a considerable attention in recent years as a drug carrier candidate for cancer treatment due to its unique structural properties and promising biocompatibility. However, its intrinsic deficiency for medical imaging potentially limits its bioapplications; To address this subject, a magnetic nano/microscale MOF has been successfully fabricated by introducing Fe(3)O(4) nanoparticles as an imaging agent into the porous isoreticular MOF [Cu(3)(BTC)(2)] as a drug carrier. The synthesized magnetic MOFs exhibits a high loading capacity (40.5%) toward the model anticancer DOX with an excellent pH-responsive drug release. The proposed nanocomposite not only possesses large surface area, high magnetic response, large mesopore volume, high transverse relaxivity (r (2)) and good stability but also exhibits superior biocompatibility, specific tumor cellular uptake, and significant cancer cell viability inhibitory effect without any targeting agent. It is expected that the synthesized magnetic nano/microcomposite may be used for clinical purposes and can also serve as a platform for photoactive antibacterial therapy ae well as pH/GSH/photo-triple-responsive nanocarrier. Frontiers Media S.A. 2023-04-04 /pmc/articles/PMC10114589/ /pubmed/37091862 http://dx.doi.org/10.3389/fmolb.2023.1071376 Text en Copyright © 2023 Gharehdaghi, Naghib, Rahimi, Bakhshi, Kefayat, shamaeizadeh and Molaabasi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Molecular Biosciences Gharehdaghi, Zahra Naghib, Seyed Morteza Rahimi, Rahmatollah Bakhshi, Atin Kefayat, Amirhosein shamaeizadeh, Armin Molaabasi, Fatemeh Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title | Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title_full | Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title_fullStr | Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title_full_unstemmed | Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title_short | Highly improved pH-Responsive anticancer drug delivery and T2-Weighted MRI imaging by magnetic MOF CuBTC-based nano/microcomposite |
title_sort | highly improved ph-responsive anticancer drug delivery and t2-weighted mri imaging by magnetic mof cubtc-based nano/microcomposite |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10114589/ https://www.ncbi.nlm.nih.gov/pubmed/37091862 http://dx.doi.org/10.3389/fmolb.2023.1071376 |
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