Cargando…

A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer

Metal–organic frameworks (MOFs), such as MIL-53(Fe), have considerable potential as drug carriers in cancer treatment due to their notable characteristics, including controllable particle sizes, high catalytic activity, biocompatibility and large porosity, and are widely used in a broad range of dru...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Anxia, Yang, Xiaoxin, Chen, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695691/
https://www.ncbi.nlm.nih.gov/pubmed/35423581
http://dx.doi.org/10.1039/d0ra09915e
_version_ 1784619633993580544
author Li, Anxia
Yang, Xiaoxin
Chen, Juan
author_facet Li, Anxia
Yang, Xiaoxin
Chen, Juan
author_sort Li, Anxia
collection PubMed
description Metal–organic frameworks (MOFs), such as MIL-53(Fe), have considerable potential as drug carriers in cancer treatment due to their notable characteristics, including controllable particle sizes, high catalytic activity, biocompatibility and large porosity, and are widely used in a broad range of drugs. In this study, a new approach for the synthesis of MIL-53(Fe) nanocrystals with controlled sizes has been developed using a non-ionic surfactant PVP as the conditioning and stabilizing agent, respectively. During the nucleation of MIL-53(Fe), the PVP droplet, as a nano-reactor, controlled the growth of the crystal nucleus. The size and aspect ratio (length/width) of nanocrystals increased with an increase in PVP in the synthetic mixture. The MIL-53(Fe) nanocrystals showed a homogeneous morphology, with approximately 190 nm in length and 100 nm in width. MIL-53(Fe) not only was used to load the anticancer drug doxorubicin (DOX) but also generated hydroxyl radicals (˙OH) via a Fenton-like reaction for ROS-mediated/chemo-therapy of cancer cells. The approach was expected to synthesize numerous types of nano-size iron(iii)-based MOFs, such as MIL-53, 89, 88A, 88B and 101. The MIL-53(Fe) nanocrystals hold great promise as a candidate to improve the controlled release of drugs and treatment effect for cancer therapy.
format Online
Article
Text
id pubmed-8695691
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-86956912022-04-13 A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer Li, Anxia Yang, Xiaoxin Chen, Juan RSC Adv Chemistry Metal–organic frameworks (MOFs), such as MIL-53(Fe), have considerable potential as drug carriers in cancer treatment due to their notable characteristics, including controllable particle sizes, high catalytic activity, biocompatibility and large porosity, and are widely used in a broad range of drugs. In this study, a new approach for the synthesis of MIL-53(Fe) nanocrystals with controlled sizes has been developed using a non-ionic surfactant PVP as the conditioning and stabilizing agent, respectively. During the nucleation of MIL-53(Fe), the PVP droplet, as a nano-reactor, controlled the growth of the crystal nucleus. The size and aspect ratio (length/width) of nanocrystals increased with an increase in PVP in the synthetic mixture. The MIL-53(Fe) nanocrystals showed a homogeneous morphology, with approximately 190 nm in length and 100 nm in width. MIL-53(Fe) not only was used to load the anticancer drug doxorubicin (DOX) but also generated hydroxyl radicals (˙OH) via a Fenton-like reaction for ROS-mediated/chemo-therapy of cancer cells. The approach was expected to synthesize numerous types of nano-size iron(iii)-based MOFs, such as MIL-53, 89, 88A, 88B and 101. The MIL-53(Fe) nanocrystals hold great promise as a candidate to improve the controlled release of drugs and treatment effect for cancer therapy. The Royal Society of Chemistry 2021-03-11 /pmc/articles/PMC8695691/ /pubmed/35423581 http://dx.doi.org/10.1039/d0ra09915e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Anxia
Yang, Xiaoxin
Chen, Juan
A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title_full A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title_fullStr A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title_full_unstemmed A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title_short A novel route to size-controlled MIL-53(Fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
title_sort novel route to size-controlled mil-53(fe) metal–organic frameworks for combined chemodynamic therapy and chemotherapy for cancer
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695691/
https://www.ncbi.nlm.nih.gov/pubmed/35423581
http://dx.doi.org/10.1039/d0ra09915e
work_keys_str_mv AT lianxia anovelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer
AT yangxiaoxin anovelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer
AT chenjuan anovelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer
AT lianxia novelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer
AT yangxiaoxin novelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer
AT chenjuan novelroutetosizecontrolledmil53femetalorganicframeworksforcombinedchemodynamictherapyandchemotherapyforcancer