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Synergistic Effects of Doxorubicin Loaded Silk Fibroin Nanoparticles and Cu-Tio2 Nanoparticles for Local Chemo-Sonodynamic Therapy Against Breast Cancer Publisher Pubmed



Maghsoudian S1, 2 ; Yektakasmaei MP3 ; Shaabani A4 ; Perseh S2 ; Fatahi Y1, 2 ; Nouri Z2, 5 ; Gholami M6 ; Sayyari N7 ; Hoseinzadeh HA8 ; Motasadizadeh H9 ; Dinarvand R1, 2, 10
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Authors Affiliations
  1. 1. Department of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Nanotechnology Research Centre, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Faculty of Veterinary Medicine, Islamic Azad University, Garmsar Branch, Garmsar, Iran
  4. 4. Department of Polymer and Materials Chemistry, Faculty of Chemistry and Petroleum Sciences, Shahid Beheshti University, Iran
  5. 5. Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  6. 6. Faculty of Pharmacy and Pharmaceutical Science Research Center, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. School of Medicine, Qom University of Medical Sciences, Qom, Iran
  8. 8. Department of Clinical Science, Faculty of Veterinary Medicine, Science and Research Branch, Islamic Azad University, Tehran, Iran
  9. 9. Medical Biomaterials Research Center, Tehran University of Medical Sciences, Tehran, Iran
  10. 10. Leicester School of Pharmacy, De Montfort University, Leicester, United Kingdom

Source: International Journal of Biological Macromolecules Published:2025


Abstract

A promising new approach to mitigate the adverse effects of chemotherapeutic drugs on healthy tissues involves combining sonodynamic therapy with topical chemotherapy to enhance the therapeutic efficacy of anticancer drugs. In this study, we introduce a multi-functional in situ chitosan hydrogel (CS) containing silk fibroin nanoparticles (SFNPs) loaded with doxorubicin (DOXSFNPs) and CuO/TiO2 nanoparticles (CTNPs) for combination therapy. The developed DOXSFNPs exhibited a size of 257 ± 6 nm, a zeta potential of −14.3 ± 1.8 mV, and a high loading capacity of 12.38 ± 1.73 %. The pH-dependent controlled release of DOX from DOXSF2/CS2 was observed to be more pronounced than that from DOX/CS2. MTT results indicated dose-dependent toxicity of CT/CS2 in response to ultrasaound radiation (US). Our findings revealed a 1.83-fold increase in reactive oxygen species (ROS) production with therapy, with the IC50 of CT3-DOXSF2/CS2-US showing a 58 % reduction compared to CT3/DOXSF2/CS2. In vivo outcomes and histopathological staining demonstrated that the CT3/DOXSF2/CS2-US treatment group exhibited the highest tumor growth inhibition rate, reaching approximately 83.65 %. These findings underscore the potential of this approach in minimizing the adverse effects of chemotherapy while maximizing therapeutic outcomes, offering a valuable contribution to the field of cancer therapy. © 2024 Elsevier B.V.
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