STUDY OF THE COMBINED EFFECT OF DOXORUBICIN-LOADED SUPERPARAMAGNETIC NANOPARTICLES AND NON-IONISING ELECTROMAGNETIC
V B Orel1, A A Chumak2, V E Orel1
1National Cancer Institute, 33/43 Yulii Zdanovskoi Str., Kyiv, 03022, Ukraine National Technical University of Ukraine «Igor Sikorsky Kyiv Polytechnic Institute», 16/2 Yangel St., 03056 Kyiv, Ukraine.
This study shows that doxorubicin-loaded superparamagnetic nanoparticles combined with electromagnetic irradiation effectively inhibit Walker256 carcinosarcoma growth. The treatment also reduced tumor heterogeneity and altered the redox state in tumors and blood.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Superparamagnetic nanoparticles offer targeted drug delivery.
- Electromagnetic irradiation can enhance therapeutic effects.
- Walker256 carcinosarcoma is a model for experimental cancer research.
Purpose of the Study:
- To investigate the combined efficacy of doxorubicin-loaded superparamagnetic nanoparticles and electromagnetic irradiation against Walker256 carcinosarcoma.
- To evaluate the impact of this magnetochemical technology on tumor growth, heterogeneity, and redox state.
Main Methods:
- Walker256 carcinosarcoma was induced in rats.
- Animals received doxorubicin-loaded superparamagnetic Fe3O4 nanoparticles and were exposed to static magnetic and electromagnetic fields.
- Tumor structural changes were assessed using MRI and texture analysis.
- Redox markers (free iron, ceruloplasmin, superoxide radical, nitric oxide) were measured using electron paramagnetic resonance spectroscopy.
Main Results:
- Combined treatment reduced tumor volume by 44-64% compared to controls.
- Texture analysis revealed decreased intratumoral heterogeneity.
- Electron paramagnetic resonance spectroscopy showed altered levels of superoxide radical, nitric oxide, and free iron in tumors and blood.
Conclusions:
- Doxorubicin-loaded superparamagnetic nanoparticles combined with electromagnetic irradiation effectively inhibit Walker256 carcinosarcoma growth.
- This approach reduces intratumoral heterogeneity.
- The treatment induces significant changes in the tumor and blood redox state.
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