# Effect of pH and (Y, Ag) co-doping on the antibacterial and toxicity properties of ZrO2 nanoparticles

**Authors:** Mehedi Hasan Jasim, Md. Iqbal Hossain, Yasfir Mahmud, A. K. M. Ahsanul Habib, Moumita Tasnim Meem

PMC · DOI: 10.1039/d5na00649j · Nanoscale Advances · 2025-09-30

## TL;DR

This study shows that Y–Ag co-doped ZrO2 nanoparticles have better antibacterial properties at higher pH and doping levels, while remaining less toxic at lower pH, making them promising for antimicrobial uses.

## Contribution

The novel contribution is the investigation of pH and Y–Ag co-doping effects on the antibacterial and toxicity properties of ZrO2 nanoparticles.

## Key findings

- Y–Ag co-doped ZrO2 nanoparticles showed superior antibacterial activity at pH 11 and 3% doping concentration.
- Toxicity increased with higher doping concentration but remained low at lower pH.
- The material is suitable for antimicrobial coatings, packaging, and textiles.

## Abstract

Nowadays, the effective bacterial inhibition and minimal toxicity properties of ZrO2 nanoparticles are creating opportunities in various applications, including biomedical, dental, antimicrobial coatings, packaging, anticancer and pesticide applications. Therefore, researchers are employing various approaches to enhance the antibacterial activity and reduce the toxicity of ZrO2 nanoparticles. In this study, undoped or pure ZrO2 nanoparticles were synthesized at different pH levels (1, 3, 7, and 11) and Y and Ag were codoped in different doping concentrations (1%, 2%, and 3%). A sucrose-assisted sol–gel method was used to synthesis both undoped and codoped ZrO2 nanoparticles. The main objective of this research was to analyze the effect of pH and codoping on the antibacterial and toxicity properties of ZrO2 nanoparticles. The synthesized particles were extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared (FTIR) spectroscopy. XRD analysis confirmed the existence of ZrO2 nanoparticles with a tetragonal structure at low pH (1 and 3), a monoclinic structure at higher pH (7 and 11) and a multiphase structure after codoping. The crystallite size of undoped ZrO2 particles increased with pH, from 8 nm at pH 1 to 20 nm at pH 11, indicating enhanced crystallinity at higher pH levels. Also, the crystallite size was 12.05, 14.81, and 11.95 nm at 1%, 2%, and 3% doping concentrations, respectively. SEM analysis revealed that the average particle size increased with increasing pH from 31.956 nm to 63.653 nm. The particle size was 34.90 nm, 48.66 nm, and 40.23 nm for 1%, 2% and 3% doped samples, respectively. The shape of the particles was irregular and mostly spherical, rod-like, and platelet-like with agglomeration. The EDX data determined the elemental composition of the particles, which indicated the successful doping with Y and Ag. The FTIR data revealed the existence of O–H, Zr–O, and other metal–oxygen vibrations in the synthesized materials. The antibacterial activity of undoped and codoped ZrO2 nanoparticles was evaluated against Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) using the disk diffusion method. The result showed that a superior antibacterial activity was observed at pH 11 for undoped particles and 3% Y–Ag codoped particles. The toxicity of the undoped and codoped ZrO2 nanoparticles was inspected using the brine shrimp lethality assay, which showed that the material was less cytotoxic at lower pH (1 and 3), and the toxicity increased with increasing doping concentration. Increasing pH and doping concentration both enhanced the antibacterial and cytotoxic activities, making the material suitable for antimicrobial coatings, packaging, and textiles, with potential for pesticide or anticancer applications pending further evaluation.

Y–Ag co-doped ZrO2 nanoparticles show enhanced anti-bacterial activity with increasing pH and doping, while their toxicity remains low at acidic pH, highlighting potential for eco-friendly anti-microbial applications.

## Linked entities

- **Chemicals:** Y (PubChem CID 23993), Ag (PubChem CID 23954), sucrose (PubChem CID 5988)

## Full-text entities

- **Diseases:** cytotoxic (MESH:D064420)
- **Chemicals:** H (MESH:D006859), sucrose (MESH:D013395), Y (MESH:D015019), Ag (MESH:D012834), Y-Ag (-), Zr (MESH:D015040), metal (MESH:D008670), O (MESH:D010100), ZrO2 (MESH:C028541)
- **Species:** Staphylococcus aureus (species) [taxon 1280], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

20 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12529584/full.md

## References

63 references — full list in the complete paper: https://tomesphere.com/paper/PMC12529584/full.md

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Source: https://tomesphere.com/paper/PMC12529584