Literature DB >> 27072712

Chemotherapeutic Approaches Against Trypanosoma evansi: Retrospective Analysis, Current Status and Future Outlook.

Nitu S Rathore, Anju Manuja1, Balvinder Kumar Manuja, Shalki Choudhary.   

Abstract

Trypanosoma evansi, the causative agent of surra, is pathogenic to a wide variety of wild and domestic animals, including equines, camels, goats, sheep, cattle, buffaloes, pigs, dogs, tigers, elephants etc. The infection is mainly restricted to animals but ability to infect human beings has also been reported due to the lack of efficient apolipoprotein L 1. The parasite is mechanically transmitted by blood-sucking flies such as Tabanus and Stomoxys species. The disease has a major economic impact in tropical countries. The control of trypanosomosis may be aimed either at the fly or against the parasite. Due to difficulties in large scale fly control, trypanocides have been widely used to control the disease. However, current chemotherapeutic agents are limited in number and usually associated with severe side effects. Moreover, current therapeutic agents are far from ideal. The emergence of drug resistant trypanosomes results in failure of prophylaxis and treatment of the disease. Retrospective and prospective studies on drug and delivery against T. evansi will provide an overview of the chemotherapeutic and prophylactic measures in vogue and suggest future strategies for combating this neglected disease. In this perspective, we have reviewed the currently used drugs available for prophylaxis and therapy, their mechanism of action and associated limitations. The options available for prophylaxis and therapy along with potential new molecules/therapeutic agents and novel approaches for delivery of the drugs to enhance their therapeutic value are presented in this review.

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Year:  2016        PMID: 27072712     DOI: 10.2174/1568026616666160413125802

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  2 in total

1.  β-Sitosterol could serve as a dual inhibitor of Trypanosoma congolense sialidase and phospholipase A2: in vitro kinetic analyses and molecular dynamic simulations.

Authors:  Suleiman Aminu; Ammar Usman Danazumi; Zainab Aliyu Alhafiz; Maria Wiktoria Gorna; Mohammed Auwal Ibrahim
Journal:  Mol Divers       Date:  2022-08-30       Impact factor: 3.364

2.  Biocompatibility and Targeting Efficiency of Encapsulated Quinapyramine Sulfate-Loaded Chitosan-Mannitol Nanoparticles in a Rabbit Model of Surra.

Authors:  Anju Manuja; Balvinder Kumar; Rajender Kumar; Meenu Chopra; Neeraj Dilbaghi; Sandeep Kumar; Suresh C Yadav
Journal:  Antimicrob Agents Chemother       Date:  2018-10-24       Impact factor: 5.191

  2 in total

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