# Evaluation of antibacterial and cytotoxic effects of silver oxide nanoparticles synthesized from Psidium Guajava

**Authors:** Abdullah Yousef, Salem S. Salem, Mohammad M. Torayah, Sara A. Saied, Rania Hamed Elbawab

PMC · DOI: 10.1038/s41598-025-24924-6 · 2025-11-25

## TL;DR

This study shows that silver oxide nanoparticles made from guava leaves are effective against drug-resistant bacteria and cancer cells, offering a green and sustainable alternative.

## Contribution

The paper introduces a green synthesis method for Ag₂O-NPs using guava leaf extract and demonstrates their dual antibacterial and anticancer potential.

## Key findings

- Ag₂O-NPs showed strong antibacterial activity against four drug-resistant bacterial strains with MIC values between 31.2 and 250 µg/mL.
- The nanoparticles exhibited selective cytotoxicity, significantly reducing HepG2 cancer cell viability with minimal impact on normal Vero cells.
- Characterization confirmed the successful synthesis of spherical Ag₂O-NPs with an average size of 25–30 nm using eco-friendly methods.

## Abstract

Growing concerns over the toxicity and environmental impact of traditional nanoparticle synthesis methods have driven the search for safer, more sustainable alternatives. At the same time, the rising prevalence of antibiotic-resistant bacteria and the ongoing challenges in effective cancer treatment emphasize the urgent need for new antimicrobial and anticancer solutions. The manufacture of silver oxide nanoparticles (Ag₂O-NPs) is investigated in this work using Psidium guajava (guava) leaves extract, focusing on their dual biological potential. The use of dangerous chemicals is reduced by this green synthesis technique by employing natural phytochemicals from guava leaves as stabilizing and reducing agents, making it more environmentally friendly compared to traditional chemical approaches. At 435 nm, the biosynthesized Ag₂O-NPs displayed a distinctive surface plasmon resonance (SPR) band. With a polydispersity index (PDI) of 0.368. Nanocrystalline, mostly spherical Ag₂O-NPs with an average size of 25 to 30 nm were successfully formed, according to thorough characterization utilizing FTIR, XRD, SEM, TEM, and EDX. These nanoparticles demonstrated strong antibacterial activity against four clinically relevant, drug-resistant bacterial strains: Pseudomonas aeruginosa ATCC 27853, Salmonella typhimurium ATCC 13311, Escherichia coli ATCC 25922, and Staphylococcus aureus ATCC 29213. Minimum inhibitory concentration (MIC) values ranged from 31.2 to 250 µg/mL, indicating a dose-dependent antibacterial action. Notably, P. aeruginosa and S. aureus showed the highest sensitivity. Cytotoxicity testing further revealed selective anticancer activity, with the Ag₂O-NPs significantly reducing the viability of HepG2 liver cancer cells (IC₅₀ = 73.93 ± 0.49 µg/mL), while displaying lower toxicity toward normal Vero cells (IC₅₀ = 158.1 ± 0.41 µg/mL). These findings suggest that green-synthesized Ag₂O-NPs hold considerable promise as both potent antibacterial agents and effective anticancer therapeutics.

The online version contains supplementary material available at 10.1038/s41598-025-24924-6.

## Linked entities

- **Chemicals:** silver oxide (PubChem CID 92152)
- **Diseases:** cancer (MONDO:0004992), liver cancer (MONDO:0002691)
- **Species:** Pseudomonas aeruginosa (taxon 287), Escherichia coli (taxon 562), Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** Cytotoxicity (MESH:D064420), cancer (MESH:D009369)
- **Chemicals:** Ag2O (MESH:C040225)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Escherichia coli (E. coli, species) [taxon 562], Pseudomonas aeruginosa (species) [taxon 287]
- **Cell lines:** HepG2 liver cancer — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), Vero — Chlorocebus sabaeus (Green monkey), Spontaneously immortalized cell line (CVCL_0059), ATCC 27853 — Homo sapiens (Human), Transformed cell line (CVCL_ZH96)

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12647600/full.md

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Source: https://tomesphere.com/paper/PMC12647600