Abstract |
Toxoplasma gondii (T. gondii) is a highly prevalent parasite that has no gold standard treatment due to the poor action or the numerous side effects. Focused sulfonamide-1,2,3-triazole hybrids 3a-c were wisely designed and synthesized via copper catalyzed 1,3-dipolar cycloaddition approach between prop-2-yn-1-alcohol 1 and sulfa drug azides 2a-c. The newly synthesized click products were fully characterized using different spectroscopic experiments and were loaded onto chitosan nanoparticles to form novel nanoformulations for further anti-Toxoplasma investigation. The current study proved the anti-Toxoplasma effectiveness of all examined compounds in experimentally infected mice. Relative to sulfadiazine, the synthesized sulfonamide-1,2,3-triazole (3c) nanoformulae demonstrated the most promising result for toxoplasmosis treatment as it resulted in 100% survival, 100% parasite reduction along with the remarkable histopathological improvement in all the studied organs.
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Authors | Faizah S Aljohani, Nadjet Rezki, Mohamed R Aouad, Bassma H Elwakil, Mohamed Hagar, Eman Sheta, Nermine Mogahed Fawzy Hussein Mogahed, Sanaa K Bardaweel, Nancy Abd-Elkader Hagras |
Journal | International journal of molecular sciences
(Int J Mol Sci)
Vol. 23
Issue 8
(Apr 11 2022)
ISSN: 1422-0067 [Electronic] Switzerland |
PMID | 35457059
(Publication Type: Journal Article)
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Chemical References |
- Antiparasitic Agents
- Sulfonamides
- Triazoles
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Topics |
- Animals
- Antiparasitic Agents
(pharmacology)
- Mice
- Sulfonamides
(pharmacology)
- Toxoplasma
- Toxoplasmosis
- Triazoles
(chemistry)
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