Comparison of biosynthetic zinc oxide nanoparticle and glucantime cytotoxic effects on Leishmania major (MRHO/IR/75/ER)

Author:

Saleh Fatemeh1ORCID,Kheirandish Farnaz23,Abbasi Mohammad1,Ahmadpour Fatemeh4,Veiskarami Saeed5,Mirderikvand Atefe1

Affiliation:

1. Razi Herbal Medicines Research Center Lorestan University of Medical Sciences Khorramabad Iran

2. Department of Medical Parasitology and Mycology, Faculty of Medicine Lorestan University of Medical Sciences Khorramabad Iran

3. Department of Medical Biotechnology, Faculty of Medicine Lorestan University of Medical Sciences Khorramabad Iran

4. Nutritional Health Research Center Lorestan University of Medical Sciences Khorramabad Iran

5. Department of Animal Science Lorestan Agricultural and Natural Resources Research and Education Center Khorramabad Iran

Abstract

AbstractCurrently, zinc oxide (ZnO) particles are used in nanotechnology to destroy a wide range of microorganisms. Although pentavalent antimony compounds are used as antileishmanial drugs, they are associated with several limitations and side effects. Therefore, it is always desirable to try to find new and effective treatments. The aim of this research is to determine the antileishmanial effect of ZnO particles in comparison to the Antimoan Meglumine compound on promastigotes and amastigotes of Leishmania major (MRHO/IR/75/ER). After the extraction and purification of macrophages from the peritoneal cavity of C57BL/6 mice, L. major parasites were cultured in Roswell Park Memorial Institute‐1640 culture medium containing fetal bovine serum (FBS) 10% and antibiotic. In this experimental study, the effect of different concentrations of nanoparticles was investigated using the 3‐[4,5‐dimethylthiazol‐2‐yl]‐2,5‐diphenyl‐tetrazolium bromide (MTT) colorimetric method, in comparison to the glucantime on promastigotes, amastigotes and healthy macrophages in the culture medium. The amount of light absorption of the obtained color from the regeneration of tetrazolium salt to the product color of formazan by the parasite was measured by an enzyme‐linked immunosorbent assay (ELISA) reader, and the IC50 value was calculated. IC50 after 24 h of incubation was calculated as IC50 = 358.6 µg/mL. The results showed, that the efficacy of ZnO nanoparticles was favorable and dose‐dependent. The concentration of 500 µg/mL of ZnO nanoparticles induced 84.67% apoptosis after 72. Also, the toxicity of nanoparticles was less than the drug. Nanoparticles exert their cytotoxic effects by inducing apoptosis. They can be suitable candidates in the pharmaceutical industry in the future.

Publisher

Wiley

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