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NIR-Responsive Methotrexate-Modified Iron Selenide Nanorods for Synergistic Magnetic Hyperthermic, Photothermal, and Chemodynamic Therapy.

Authors :
Thirumurugan S
Muthiah KS
Lin YC
Dhawan U
Liu WC
Wang AN
Liu X
Hsiao M
Tseng CL
Chung RJ
Source :
ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 May 22; Vol. 16 (20), pp. 25622-25636. Date of Electronic Publication: 2024 May 13.
Publication Year :
2024

Abstract

Breast cancer is a malignant tumor with a high mortality rate among women. Therefore, it is necessary to develop novel therapies to effectively treat this disease. In this study, iron selenide nanorods (FeSe <subscript>2</subscript> NRs) were designed for use in magnetic hyperthermic, photothermal, and chemodynamic therapy (MHT/PTT/CDT) for breast cancer. To illustrate their efficacy, FeSe <subscript>2</subscript> NRs were modified with the chemotherapeutic agent methotrexate (MTX). MTX-modified FeSe <subscript>2</subscript> (FeSe <subscript>2</subscript> -MTX) exhibited excellent controlled drug release properties. Fe <superscript>2+</superscript> released from FeSe <subscript>2</subscript> NRs induced the release of <superscript>•</superscript> OH from H <subscript>2</subscript> O <subscript>2</subscript> via a Fenton/Fenton-like reaction, enhancing the efficacy of CDT. Under alternating magnetic field (AMF) stimulation and 808 nm laser irradiation, FeSe <subscript>2</subscript> -MTX exerted potent hyperthermic and photothermal effects by suppressing tumor growth in a breast cancer nude mouse model. In addition, FeSe <subscript>2</subscript> NRs can be used for magnetic resonance imaging in vivo by incorporating their superparamagnetic characteristics into a single nanomaterial. Overall, we presented a novel technique for the precise delivery of functional nanosystems to tumors that can enhance the efficacy of breast cancer treatment.

Details

Language :
English
ISSN :
1944-8252
Volume :
16
Issue :
20
Database :
MEDLINE
Journal :
ACS applied materials & interfaces
Publication Type :
Academic Journal
Accession number :
38739745
Full Text :
https://doi.org/10.1021/acsami.3c18450