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Highly effective suppression of herpes simplex virus type 1 by titanium dioxide nanoparticles
Abdulhussain Kadhim Jwaziri1, Pegah Khales2, Zahra Salavatiha3
1Department of Microbiology, College of Medicine, University of Kerbala, Karbala, Iraq.
Virology
|March 29, 2026
Summary
Titanium dioxide (TiO2) nanoparticles show significant antiviral activity against Herpes simplex virus type 1 (HSV-1) in cell cultures. These TiO2 nanoparticles demonstrate good biocompatibility, offering a promising new avenue for antiviral therapy.
Area of Science:
- Nanotechnology
- Virology
- Biocompatibility
Background:
- Herpes simplex virus type 1 (HSV-1) presents a significant clinical challenge due to drug resistance and infection recurrence.
- Novel antiviral agents are crucial for managing HSV-1 infections.
- Titanium dioxide (TiO2) nanoparticles are explored for their potential antiviral properties, owing to their photocatalytic activity, low toxicity, and biocompatibility.
Purpose of the Study:
- To investigate the antiviral efficacy of TiO2 nanoparticles against HSV-1.
- To evaluate the biocompatibility of TiO2 nanoparticles on Vero cells.
Main Methods:
- Characterization of TiO2 nanoparticles using X-ray diffraction, FTIR spectroscopy, zeta potential, and SEM.
- Cytotoxicity assessment on Vero cells via neutral red assay.
- Evaluation of antiviral activity through virucidal and post-treatment assays, with viral load quantified by real-time PCR.
Main Results:
- TiO2 nanoparticles exhibited no cytotoxicity at concentrations up to 1200 μg/mL.
- Significant HSV-1 inhibition was observed: 95.1% at 400 μg/mL, 98% at 800 μg/mL, and 98.8% at 1200 μg/mL in virucidal tests.
- Post-treatment tests showed even higher inhibition rates, reaching 99.9% at 1200 μg/mL.
Conclusions:
- TiO2 nanoparticles demonstrate potent in vitro antiviral efficacy against HSV-1 in Vero cells.
- The nanoparticles exhibit favorable biocompatibility at concentrations effective for antiviral activity.
- Further in vivo studies are warranted to elucidate the antiviral mechanisms of TiO2 nanoparticles.
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