Pharmacological activity and targeted delivery of supramolecular fenbendazole obtained by mechanochemical technology with various components

Author:

Varlamova A. I.1,Arkhipov I. A.1,Abramov V. E.1,Arisov M. V.1,Khalikov S. S.2,Dushkin A. V.3

Affiliation:

1. All-Russian Scientific Research Institute for Fundamental and Applied Parasitology of Animals and Plant – a branch of the Federal State Budget Scientific Institution "Federal Scientific Centre VIEV"

2. A. N. Nesmeyanov Institute of Organoelement Compounds RAS

3. Institute of Solid-State Chemistry and Mechanochemistry, Siberian Branch of the Russian Academy of Sciences

Abstract

The purpose of the research is studying the influence of various components on the targeted delivery of fenbendazole and evaluation of their efficacy in mice experimentally infected with Trichinella spiralis.Materials and methods. The experiment used 80 white mice experimentally infected with T. spiralis, at a dose of 200 larvae per animal. Each group of 10 animals was administered intragastrically solid dispersion of fenbendazole (SDF) with polyvinyl pyrrolidone (PVP), arabinogalactan (AG), disodium salt of glycyrrhizinic acid (Na2 GA), sodium dioctyl sulfosuccinate (SDS), licorice extract (LE) and hydroxyethyl starch (HES) at a single dose of 2.0 mg/kg of active substance as compared with the fenbendazole substance at the same dose. The control group did not receive the drug. The anthelmintic efficacy was studied by the results of necropsy of the small intestine of mice on the second day after drugs administration. The concentration of fenbendazole and its metabolites in the small intestine was determined by high-performance liquid chromatography with tandem mass spectrometry detection.Results and discussion. SDF with PVP, AG, Na2 GA, SDS, LE and HES showed 98.0, 94.9, 96.6, 100, 86.0 and 81.0% efficacy against intestinal nematode T. spiralis at a dose of 2.0 mg/kg of AS (fenbendazole). The maximum concentration of fenbendazole and its metabolites – sulfone and sulfoxide - was determined in the small intestine wall of animals on the second day after SDF with SDS administration and amounted to 3117.8, 614.6 and 2998.6 ng/g respectively. After fenbendazole substance administration, the drug and its metabolites were found in trace quantity. 

Publisher

Institute of Fundamental and Applied Parasitology of Animals and Plants

Reference23 articles.

1. Arkhipov I. A. Anthelmintics: pharmacology and application. М., 2009; 409. (In Russ.)

2. Arkhipov I. A., Khalikov S. S., Dushkin A. V., Varlamova A. I., Musaev M. B., Polyakov N. E., Chistyachenko Yu. S., Sadov K. M., Khalikov M. S. Supramolecular complexes of anthelmintic benzimidazole-based drugs. Obtaining and properties. M.: New authors, 2017; 91. (In Russ.)

3. Astafiev B. A., Yarotsky L. S., Lebedeva M. N. Experimental models of parasitoses in biology and medicine. М., 1989; 279. (In Russ.)

4. Varlamova A. I., Limova Yu. V., Sadov K. M., Sadova A. K., Belova E. E., Radionov A. V., Khalikov S. S., Chistyachenko Yu. S., Dushkin A. V., Skira V. N., Arkhipov I. A. Efficacy of the supramolecular complex of fenbendazole against nematodiases of sheep. Rossiyskiy parazitologicheskiy zhurnal = Russian Journal of Parasitology. 2016; 35 (1): 76-81. (In Russ.)

5. Varlamova A. I. Anthelmintic efficacy of the supramolecular complex of fenbendazole against nematodoses of young cattle. Veterinariya = Journal of Veterinary Medicine. 2017; 1: 32-35. (In Russ.)

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