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Development of Core@Shell γ-Fe 2 O 3 @Mn x O y @SiO 2 Nanoparticles for Hyperthermia, Targeting, and Imaging Applications.

Authors :
Joshi R
Shelar SB
Srivastava M
Singh BP
Goel L
Ningthoujam RS
Source :
ACS applied bio materials [ACS Appl Bio Mater] 2022 Nov 21; Vol. 5 (11), pp. 5386-5393. Date of Electronic Publication: 2022 Nov 09.
Publication Year :
2022

Abstract

Monodispersed core@shell γ-Fe <subscript>2</subscript> O <subscript>3</subscript> @Mn <subscript> x </subscript> O <subscript> y </subscript> nanoparticles have been prepared through thermolysis of iron and manganese oleate. Further, these prepared nanoparticles are coated with biocompatible substances such as silica and polyethylene glycol. These particles are highly biocompatible for different cell lines such as normal and cancer cell lines. The nanoparticles are used as hyperthermia agents, and successful hyperthermia treatment in cancer cells is carried out. As compared to γ-Fe <subscript>2</subscript> O <subscript>3</subscript> @SiO <subscript>2</subscript> , γ-Fe <subscript>2</subscript> O <subscript>3</subscript> @Mn <subscript> x </subscript> O <subscript> y </subscript> @SiO <subscript>2</subscript> shows the enhanced killing of cancer cells through hyperthermia. In order to make them potential candidates for targeting to cancer cells, folic acid (FA) is tagged to the nanoparticles. Fluorescein isothiocyanate (FITC) is also tagged onto these nanoparticles for imaging. The developed γ-Fe <subscript>2</subscript> O <subscript>3</subscript> @Mn <subscript> x </subscript> O <subscript> y </subscript> @SiO <subscript>2</subscript> nanoparticle can act as a single entity for therapy through AC magnetic field, imaging through FITC and targeting through folic acid simultaneously. This is the first report on this material, which is highly biocompatible for hyperthermia, imaging, and targeting.

Details

Language :
English
ISSN :
2576-6422
Volume :
5
Issue :
11
Database :
MEDLINE
Journal :
ACS applied bio materials
Publication Type :
Academic Journal
Accession number :
36350576
Full Text :
https://doi.org/10.1021/acsabm.2c00758