Synthesis, characterization, and antiparasitic effects of zinc oxide nanoparticles-eugenol nanosuspension against Toxoplasma gondii infection

Kourosh Cheraghipour; Amal Khudair Khalaf; Kobra Moradpour; Masoomeh Zivdari; Marjan Beiranvand; Pegah Shakib; Hossein Mahmoudvand; Abdolrazagh Marzban

doi:10.1016/j.heliyon.2023.e19295

Synthesis, characterization, and antiparasitic effects of zinc oxide nanoparticles-eugenol nanosuspension against Toxoplasma gondii infection

Heliyon. 2023 Aug 19;9(8):e19295. doi: 10.1016/j.heliyon.2023.e19295. eCollection 2023 Aug.

Authors

Kourosh Cheraghipour¹, Amal Khudair Khalaf², Kobra Moradpour¹, Masoomeh Zivdari¹, Marjan Beiranvand¹, Pegah Shakib¹, Hossein Mahmoudvand³, Abdolrazagh Marzban¹

Affiliations

¹ Razi Herbal Medicines Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran.
² Department of Microbiology, College of Medicine, University of Thiqar, Iraq.
³ Hepatitis Research Center, Lorestan University of Medical Sciences, Khorramabad, Iran.

Abstract

Background: In this study, zinc oxide nanoparticles-coated with eugenol (ZnO@Eug) were synthesized and evaluated as a nanosuspension (NSus) formulation against Toxoplasma gondii in vitro and in vivo.

Methods: An anti-Toxoplasma activity assay for ZnO@Eug NSus was conducted in vitro, ex vivo, and in vivo. FTIR spectroscopy confirmed the formation of ZnO@Eug NSus by detecting several functional groups involved; EDX and SEM demonstrated the grain of ZnO-NPs embedded with Eug and compositional purity.

Results: Surface charge (ZP) and size distribution (DLS) of ZnO@Eug NSus were determined to be -22.7 mV and 109.6 nm, respectively. According to the release kinetics, approximately 60% of the ZnO-NPs and Eug were released in the first 45 min. In the cytotoxicity assay, ZnO-NPs, Eug, and ZnO@Eug NSus had IC₅₀ values of 71.85, 22.39, and 2.02 mg/mL, respectively. The therapeutic efficacy of ZnO@Eug against T. gondii was 56.3%, which was not significantly different from that of spiramycin (58.9%) (Positive-control). The tissue tachyzoites in the liver, spleen, and peritoneum were less than 50% in groups treated with Eug, spiramycin, and ZnO@Eug NSus compared to the control. ZnO@Eug-treated groups showed a survival rate of up to 13 days.

Conclusions: The ZnO@Eug NSus demonstrated antiparasitic activity against T. gondii with minimal toxic effects and high efficiency in increasing the survival of infected mice. The nanoformulations of ZnO-NPs incorporated with Eug could, in the future, be considered for treating toxoplasmosis in humans and animals if a detailed study was conducted to determine the precise dose and measure side effects.

Keywords: Antiparasitic activity; Eugenol; Toxoplasma gondii; Zinc oxid nanoparticles; ZnO@Eug NSus.