Thymoquinone-Loaded Zinc Nanoparticles Mitigate Inflammation and Inhibit Glioblastoma Progression: A Novel Therapeutic Approach
Sofia Sebastian1, Taniya Mary Martin2, Meenakshi Sundaram Kishore Kumar2★★ Corresponding author
- 1Department of Oral and Maxillofacial Pathology and Microbiology, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, Tamil Nadu, INDIA.
- 2Department of Anatomy, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, Tamil Nadu, INDIA.
CORRESPONDENCE
Meenakshi Sundaram Kishore Kumar
Department of Anatomy, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, Tamil Nadu, INDIA.
Received: 19-02-2025; Revised: 29-04-2025; Accepted: 02-06-2025.
Volume 17, Issue 3 · pp. 850–858 · PUBLISHED Jul-Sep 2025 · DOI: 10.5530/pres.20252143
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ABSTRACT
Background Glioblastoma is the most aggressive and lethal primary brain tumour, characterized by rapid proliferation, high invasiveness, and resistance to conventional therapies. Chronic inflammation plays a crucial role in its progression, with pro-inflammatory cytokines contributing to tumour growth and therapy resistance. Nanotechnology based approaches, such as Thymoquinone derived Zinc Nanoparticles (TQ-ZnNPs) offer a promising strategy to enhance drug bioavailability and target inflammation driven glioblastoma more effectively. Objectives Thymoquinone, a naturally occurring substance with anti-inflammatory and anticancer qualities, has drawbacks such as low bioavailability and solubility. To overcome these, TQ-ZnNPs were synthesized using nanotechnology. Materials and Methods TQ-ZnNPs were synthesized using a green nanotechnology approach and characterized for their physicochemical properties through techniques like, Scanning Electron Microscopy (SEM), Fourier-Transform Infrared spectroscopy (FTIR), X-ray Diffraction (XRD) and Ultraviolet-visible (UV-vis) spectroscopy examination to verify their optical and structural characteristics. Glioblastoma cells were treated with Lipopolysaccharide to induce inflammation, followed by exposure to TQ-ZnNPs to assess their anti-inflammatory and anti-cancer effects. RT-PCR method was used to assess gene expression. Results TQ-ZnNPs exhibited enhanced stability and bioavailability, significantly reducing oxidative stress and suppressing pro-inflammatory cytokine expression in glioblastoma cells. They effectively inhibited cell proliferation and induced apoptosis, suggesting potent anti-inflammatory and anti-cancer properties. These findings highlight the therapeutic potential of TQ-ZnNPs in targeting inflammation driven glioblastoma. Conclusion TQ-ZnNPs demonstrate significant anti-inflammatory and anti-cancer potential, making them a promising nanotherapeutic approach for combating inflammation driven glioblastoma.
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Sebastian, S., Martin, T. M., & Kumar, M. S. K. (2025). Thymoquinone-Loaded Zinc Nanoparticles Mitigate Inflammation and Inhibit Glioblastoma Progression: A Novel Therapeutic Approach. Pharmacognosy Research, 17(3), 850–858. https://doi.org/10.5530/pres.20252143
