| Literature DB >> 35299902 |
Amal Farahat Allam1, Nancy Abd-Elkader Hagras2, Hoda Fahmy Farag1, Mervat Mostafa Osman1, Thanaa Ibrahim Shalaby3, Amani Hussein Kazem4, Amel Youssef Shehab1, Nermine Mogahed Fawzy Hussein Mogahed5.
Abstract
The present study investigated the anti-Toxoplasma effect of chitosan nanoparticles [CS NPs], spiramycin, spiramycin co-administered with metronidazole and spiramycin-CS NPs formulation on the parasite burden and histopathological changes in the liver, spleen and brain in experimentally infected mice. Seventy male Swiss albino mice were classified into seven equal groups: healthy control (I), infected untreated control (II), infected group receiving CS NPs (III), spiramycin administered infected group (IV), infected group receiving spiramycin-metronidazole (V), infected receiving 400 mg/kg spiramycin-CS NPs (VI) and infected treated with spiramycin-loaded CS NPs 100 mg/kg (VII). All groups were inoculated intraperitoneally with 2500 T. gondii tachyzoites RH strain except the healthy control group. All groups were sacrificed on the 8th day after infection. Density of the parasite and histopathological examination of the liver, spleen and brain of all treated mice revealed reduction in the mean tachyzoites count as well as decreased inflammation, congestion and necrosis within tissue sections. Spiramycin-loaded NPs displayed the highest significant reduction in the pathological insult tailed by spiramycin-metronidazole and CS NPs. In conclusion, spiramycin-loaded CS NPs showed a promising synergistic combination in the treatment of the histopathology caused by toxoplasmosis. © Indian Society for Parasitology 2021.Entities:
Keywords: Chitosan nanoparticles; Spiramycin; Spiramycin-chitosan nanoparticles formulation; Spiramycin-metronidazole; Toxoplasma gondii
Year: 2021 PMID: 35299902 PMCID: PMC8901813 DOI: 10.1007/s12639-021-01431-9
Source DB: PubMed Journal: J Parasit Dis ISSN: 0971-7196