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[T-weighted magnetic resonance imaging contrast agents and their theranostic nanoprobes].

作者信息

Zhou Huimin, Qiu Xiaozhong, Shen Zheyu

机构信息

Biomaterials Research Center, School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2020 Mar 30;40(3):427-444. doi: 10.12122/j.issn.1673-4254.2020.03.24.


DOI:10.12122/j.issn.1673-4254.2020.03.24
PMID:32376585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7167323/
Abstract

Magnetic resonance imaging (MRI) is an important imaging modality for clinical disease diagnosis, and nearly 50% of clinical MRI examinations require contrast agents to enhance the diagnostic sensitivity. This review provides a summary of the major MRI contrast agents and their classification, and the advantages and limits of the commercially available MRI contrast agents, and elaborates on the exceedingly small magnetic iron oxide nanoparticles (ES-MIONs), dotted core-shell iron and gadolinium hybrid nanoparticles (FeGd-HN) and exceedingly small gadolinium oxide nanoparticles (ES-GON). These nanoparticles can greatly improve the efficiency of T-weighted MRI due to their high value and low / ratio, and are expected to be translated into clinical contrast agents for T-weighted MRI. The authors also review the diagnostic and therapeutic integration system that combines MRI contrast agents with various tumor therapies, such as MRI-guided ferroptosis therapy, radiosensitization therapy, and photothermal therapy, which allow efficient treatment as well as real-time monitoring of tumors and serve as potential cancer therapy strategies. The possible future research directions in the field of MRI-based multifunctional diagnostic and therapeutic formulations are also discussed.

摘要

相似文献

[1]
[T-weighted magnetic resonance imaging contrast agents and their theranostic nanoprobes].

Nan Fang Yi Ke Da Xue Xue Bao. 2020-3-30

[2]
Multifunctional Theranostic Nanoparticles Based on Exceedingly Small Magnetic Iron Oxide Nanoparticles for T-Weighted Magnetic Resonance Imaging and Chemotherapy.

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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引用本文的文献

[1]
VHPKQHR Peptide Modified Ultrasmall Paramagnetic Iron Oxide Nanoparticles Targeting Rheumatoid Arthritis for T-Weighted Magnetic Resonance Imaging.

Front Bioeng Biotechnol. 2022-2-28

[2]
[Mn-doped Prussian blue nanoparticles for T1-T2 dual-mode magnetic resonance imaging and photothermal therapy ].

Nan Fang Yi Ke Da Xue Xue Bao. 2021-6-20

本文引用的文献

[1]
Silica-coated super-paramagnetic iron oxide nanoparticles (SPIONPs): a new type contrast agent of T magnetic resonance imaging (MRI).

J Mater Chem B. 2015-7-14

[2]
Small-sized gadolinium oxide based nanoparticles for high-efficiency theranostics of orthotopic glioblastoma.

Biomaterials. 2020-3

[3]
On-Demand Biodegradable Boron Nitride Nanoparticles for Treating Triple Negative Breast Cancer with Boron Neutron Capture Therapy.

ACS Nano. 2019-11-11

[4]
Exceedingly Small Gadolinium Oxide Nanoparticles with Remarkable Relaxivities for Magnetic Resonance Imaging of Tumors.

Small. 2019-8-25

[5]
ROS-Responsive Polymeric siRNA Nanomedicine Stabilized by Triple Interactions for the Robust Glioblastoma Combinational RNAi Therapy.

Adv Mater. 2019-7-26

[6]
Emerging blood-brain-barrier-crossing nanotechnology for brain cancer theranostics.

Chem Soc Rev. 2019-6-4

[7]
Scaffolds biomimicking macrophages for a glioblastoma NIR-Ib imaging guided photothermal therapeutic strategy by crossing Blood-Brain Barrier.

Biomaterials. 2019-5-6

[8]
Radiation-Induced Targeted Nanoparticle-Based Gene Delivery for Brain Tumor Therapy.

ACS Nano. 2019-3-27

[9]
Inducing a Transient Increase in Blood-Brain Barrier Permeability for Improved Liposomal Drug Therapy of Glioblastoma Multiforme.

ACS Nano. 2018-12-19

[10]
Apolipoprotein E Peptide-Directed Chimeric Polymersomes Mediate an Ultrahigh-Efficiency Targeted Protein Therapy for Glioblastoma.

ACS Nano. 2018-11-8

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