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Published on: September 27, 2024
Zinc oxide nanoparticles from drug delivery to immunomodulation: progress and challenges
Marzia Conte1, Veronica Vighetto1, Valentina Cauda1
1Department of Applied Science and Technology, Politecnico di Torino, Turin, Italy.
Zinc oxide nanoparticles (ZnO NPs) show promise in cancer therapy by delivering drugs and boosting the immune system. Further research is needed for clinical use.
Area of Science:
- Nanomedicine
- Biomedical Engineering
- Oncology
Background:
- Zinc oxide nanoparticles (ZnO NPs) are increasingly recognized for their potential in diverse biomedical applications.
- Their unique properties make them suitable for advanced cancer treatment strategies.
- This review focuses on the application of ZnO NPs in cancer therapy.
Purpose of the Study:
- To critically review the main uses of ZnO NPs in cancer therapy.
- To highlight their roles in drug delivery, stimuli-responsive systems, and immunomodulatory treatments.
- To discuss their potential for targeting tumor tissues.
Main Methods:
- Analysis of ZnO NP properties, including dissolution in acidic tumor microenvironments and generation of radical oxygen species.
- Review of engineered multimodal nanoplatforms combining ZnO NPs with chemotherapy, immunotherapy, photodynamic, and sonodynamic therapies.
- Evaluation of ZnO NP immunomodulatory capabilities, including T-cell activation and dendritic cell maturation.
Main Results:
- ZnO NPs induce cancer cell apoptosis through metabolic dysregulation in the tumor microenvironment.
- Multimodal nanoplatforms with ZnO NPs achieve synergistic antitumor effects, addressing limitations of current therapies.
- ZnO NPs possess strong immunomodulatory capabilities, potentially reversing 'cold' tumor microenvironments.
Conclusions:
- ZnO NPs present revolutionary therapeutic prospects for novel anti-cancer treatments.
- Their ability to enhance drug delivery, create stimuli-responsive systems, and modulate the immune response is significant.
- Addressing challenges in long-term stability and controlled degradability is crucial for clinical translation.
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