Chemical characterization and anti‐hemolytic anemia potentials of tin nanoparticles synthesized by a green approach for bioremediation applications

Abstract

The therapeutic properties of tin nanoparticles have been proved in recent years. One of their probable effects is anti‐anemia. In this study, tin nanoparticles were synthesized and characterized in aqueous medium using Ziziphora clinopodioides Lam leaf aqueous extract as the reducing and stabilizing agent. We also assessed the antihemolytic anemia potential of tin nanoparticles (SnNPs) in an animal model of hemolytic anemia. Tin nanoparticles were characterized using many techniques including Fourier transform‐infrared and UV‐visible spectroscopy, X‐ray diffraction (XRD), energy dispersive X‐ray spectrometry, and field emission‐scanning electron microscopy (FE‐SEM). FE‐SEM images showed a uniform spherical morphology in size of 18.12 nm for the green synthesized nanoparticles. According to XRD analysis, SnNPs crystal size was17.94 nm. SnNPs had low cell viability dose‐dependently against human umbilical vein endothelial cell line. in vivo design, induction of hemolytic anemia was done by phenylhydrazine in 40 mice. Tin nanoparticles significantly (p ≤ 0.01) reduced the weight and volume of liver and spleen and the concentration of pro‐inflammatory cytokines, and increased the body weight, anti‐inflammatory cytokines concentration, total platelet, WBC, neutrophil, lymphocyte, eosinophil, monocyte, and basophil counts, and red blood cell parameters compared to the untreated mice. For the biochemical parameters, SnNPs significantly (p ≤ 0.01) increased the concentrations of GPx, CAT, and SOD in serum, liver, and spleen and decreased the concentration of GR in serum, liver, and spleen, and also erythropoietin, ferritin, and ferrous in serum as compared to the anemic mice. The 2,2‐diphenyl‐1‐picrylhydrazyl test showed similar antioxidant activities for SnNPs and butylated hydroxytoluene. The results demonstrate the excellent antihemolytic anemia, hematoprotective, cytotoxicity, and antioxidant potentials of SnNPs compared to other experimental groups.

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