Glucosamine Conjugated Gadolinium (III) Oxide Nanoparticles as a Novel Targeted Contrast Agent for Cancer Diagnosis in MRI

Glucose transporter (Glut), a cellular transmembrane receptor, has a key role in the metabolism of cell glucose and is also associated with various human carcinomas. In this study, we evaluated a magnetic resonance (MR) imaging contrast agent for tumor detection based on paramagnetic gadolinium oxid...

Full description

Saved in:
Bibliographic Details
Published inJournal of biomedical physics and engineering Vol. 10; no. 1; pp. 25 - 38
Main Authors T, Mortezazadeh, E, Gholibegloo, N, Riyahi Alam, S, Haghgoo, A E, Musa, M, Khoobi
Format Journal Article
LanguageEnglish
Published Iran Shiraz University of Medical Sciences 01.02.2020
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Glucose transporter (Glut), a cellular transmembrane receptor, has a key role in the metabolism of cell glucose and is also associated with various human carcinomas. In this study, we evaluated a magnetic resonance (MR) imaging contrast agent for tumor detection based on paramagnetic gadolinium oxide (Gd O ) coated polycyclodextrin (PCD) and modified with glucose (Gd O @PCD-Glu) for the targeting of overexpressed glucose receptors. In this experimental study, 3T magnetic resonance imaging (MRI) scanner was used to assess the specific interactions between Glut1-overexpressing tumor cells (MDA-MB-231) and Gd O @PCD-Glu NPs. Furthermore, the capacity of transporting Gd O @PCD-Glu NPs to tumor cells was evaluated. It was found that the acquired MRI T signal intensity of MDA-MB-231 cells that were treated with the Gd O @PCD-Glu NPs increased significantly. Based on the results obtained, Gd O @PCD-Glu NPs can be applied in targeting Glut1-overexpressing tumor cells in vivo, as well as an MRI-targeted tumor agent to enhance tumor diagnosis. Results have shown that glucose-shell of magnetic nanoparticles has a key role in diagnosing cancer cells of high metabolic activity.
ISSN:2251-7200
2251-7200
DOI:10.31661/jbpe.v0i0.1018