Antiviral Potential Efficacy of Green-Synthesized Silver and Titanium Dioxide Nanoparticles Against Rotavirus, Cytomegalovirus, and Human Papillomavirus
Authors:
- Mohamed Z. Sayed-AhmedMohamed Z. Sayed-Ahmed
- Mohamed A. RizkMRMohamed A. Rizk
- Soheir A. A. HagrasSHSoheir A. A. Hagras
- Moaddey AlfarhanMAMoaddey Alfarhan
- Ayed A. AlshamraniAAAyed A. Alshamrani
- Ahmed H. AlbariqiAAAhmed H. Albariqi
- Amal A. MohamedAMAmal A. Mohamed
- Mostafa A. Abdel-MaksoudMAMostafa A. Abdel-Maksoud
- Wahidah H. Al-QahtaniWAWahidah H. Al-Qahtani
- Bushra Hafeez KianiBKBushra Hafeez Kiani
- Atef S. ElgebalyAEAtef S. Elgebaly
Open Access
- 31 March 2026
- journal article
- research article
- Published by MDPI AG in Pharmaceuticals
- Vol. 19 (4) , 556
Abstract
Background: Viral infections represent a major challenge in modern medicine, including diseases caused by human papillomavirus (HPV), cytomegalovirus (CMV), and rotavirus, which are among the most prevalent viral pathogens. The rapid transmission and high mutation rates of these viruses contribute to substantial health burdens and socio economic consequences. Silver nanoparticles (Ag NPs) and titanium dioxide nanoparticles (TiO2-NPs) are effective antiviral agents. The major objective of this investigation was to measure the antiviral activity of titanium dioxide nanoparticles (TiO2-NPs) and green-produced silver nanoparticles (Ag NPs) against rotavirus, HPV, and CMV. Methods: UV-Vis spectroscopy, transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) were used to characterize the nanoparticles. Cytotoxicity and antiviral activity were evaluated using a crystal violet assay in infected cell cultures. Results: The main findings indicate that both Ag NPs and TiO2-NPs exhibited pronounced antiviral activity against HPV, CMV, and rotavirus. Ag NPs exhibited strong antiviral activity, with lower IC50 values against HPV and CMV; however, this effect was associated with lower cytotoxic concentration (CC50) and selectivity index (SI) values, indicating higher cytotoxicity. In contrast, TiO2-NPs demonstrated a favorable safety profile, as indicated by higher CC50 value particularly against CMV (863.90 µg/mL) and rotavirus (386.84 µg/mL)—and low cytotoxicity toward host cells—highlighting their strong antiviral selectivity and therapeutic potential. Conclusions: Overall, these findings suggest that, while Ag-NPs possess strong antiviral efficacy, TiO2 NPs offer a more balanced combination of antiviral effectiveness and biosafety and may therefore be more promising candidates for antiviral applications.Keywords
Funding Information
- Deanship of Scientific Research, Vice Presidency for Graduate Studies and Scientific Research, King Faisal University, (KFU261595)
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