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Remarkable histopathological improvement of experimental toxoplasmosis after receiving spiramycin-chitosan nanoparticles formulation.
Allam, Amal Farahat; Hagras, Nancy Abd-Elkader; Farag, Hoda Fahmy; Osman, Mervat Mostafa; Shalaby, Thanaa Ibrahim; Kazem, Amani Hussein; Shehab, Amel Youssef; Mogahed, Nermine Mogahed Fawzy Hussein.
Afiliação
  • Allam AF; Department of Parasitology, Medical Research Institute, Alexandria University, 165 El Horreya Avenue, El Hadara, Alexandria, Egypt.
  • Hagras NA; Department of Medical Laboratory, Faculty of Applied Health Sciences Technology, Pharos University in Alexandria, Alexandria, Egypt.
  • Farag HF; Department of Parasitology, Medical Research Institute, Alexandria University, 165 El Horreya Avenue, El Hadara, Alexandria, Egypt.
  • Osman MM; Department of Parasitology, Medical Research Institute, Alexandria University, 165 El Horreya Avenue, El Hadara, Alexandria, Egypt.
  • Shalaby TI; Department of Medical Biophysics, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Kazem AH; Department of Pathology, Medical Research Institute, Alexandria University, Alexandria, Egypt.
  • Shehab AY; Department of Parasitology, Medical Research Institute, Alexandria University, 165 El Horreya Avenue, El Hadara, Alexandria, Egypt.
  • Mogahed NMFH; Department of Medical Parasitology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
J Parasit Dis ; 46(1): 166-177, 2022 Mar.
Article em En | MEDLINE | ID: mdl-35299902
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.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Idioma: En Revista: J Parasit Dis Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 2_ODS3 / 3_ND Base de dados: MEDLINE Idioma: En Revista: J Parasit Dis Ano de publicação: 2022 Tipo de documento: Article