Innovative anthelmintic based on mechanochemical technology and their efficacy against parasitic infection of sheeps

Authors

  • Victor A Marchenko Department of Gorno-Altay Research Institute of Agriculture, Federal Altai Scientific Center of Agrobiotechnology, Barnaul, Russia.
  • Salavat S Khalikov Laboratory for Physiologically Active Organofluorine Compounds, Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Science, Moscow, Russia.
  • Yury A Vasilenko Department of Gorno-Altay Research Institute of Agriculture, Federal Altai Scientific Center of Agrobiotechnology, Barnaul, Russia.
  • Mikhail M Ilyin Laboratory for Physiologically Active Organofluorine Compounds, Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Science, Moscow, Russia.
  • Irina A Kravchenko Faculty of Veterinary Medicine, Altai State Agricultural University, Barnaul, Russia.

Keywords:

Fenbendazole; ivermectin; triclabendazole; parasitocidal activity; solid dispersions

Abstract

Objective: Solubility and bioavailability are crucial for maximizing the activity of an antiparasitic drug. This study aimed to develop a combined preparation for antiparasitic medicines using iver­mectin (Iver), fenbendazole (FBZ), and triclabendazole (TBZ), considering their solubility, bioavail­ability, and activity.  Materials and Methods: Innovative preparations in solid dispersions (SD) were obtained using the joint mechanical processing of drug substances with polyvinylpyrrolidone (PVP) in an LE-101 roller mill. The preparations’ efficacy was studied in 140 sheep spontaneously infected with gastroin­testinal Strongylata, Dicrococelium dendriticum, Moniezia expansa, and Melophagus ovinus. The preparations were given individually to the sheep in the form of an aqueous suspension orally. Their effectiveness was evaluated using intravital and postmortem parasitological examinations.  Results: The results confirmed the increase in solubility of substances by 13–29 times. The exper­iments have shown the high efficacy of SD composition of FBZ/Iver/PVP (1/1/9) containing FBZ (at 3.0 mg/kg b/w) and Iver (at 0.2 mg/kg b/w) when used against gastrointestinal Strongylates and M. expansa (95.8% and 100%, respectively), to a lesser extent against M. ovinus (38.5%). The SD composition of TBZ/Iver/PVP (1/1/9) of TBZ (at 3.0 mg/kg b/w) and Iver (at 0.2 mg/kg b/w) showed a high efficacy against gastrointestinal Strongylata and D. dendriticum (96.8% and 100%, respectively) and less activity against M. ovinus (61.6%).  Conclusion: The high parasiticidal activity of SD based on FBZ, TBZ, and Iver in comparison with initial substances is explained by the formation of inclusion complexes of these substances with PVP when SD is dissolved in water and the synergistic effect of the active substances of the prepa­rations. The resulting complexes have increased solubility in water and bioavailability. The use of such an SD suggests a significant reduction in the dosages of FBZ and TBZ without losing parasit­icidal activity.

J. Adv. Vet. Anim. Res., 7(4): 718-725, Dec 2020

http://doi.org/10.5455/javar.2020.g473

Downloads

Download data is not yet available.
Abstract
27
PDF
15

Downloads

Published

2020-12-03

How to Cite

Marchenko, V. A., Khalikov, S. S., Vasilenko, Y. A., Ilyin, M. M., & Kravchenko, I. A. (2020). Innovative anthelmintic based on mechanochemical technology and their efficacy against parasitic infection of sheeps. Journal of Advanced Veterinary and Animal Research, 7(4), 718–725. Retrieved from https://banglajol.info/index.php/JAVAR/article/view/75901

Issue

Vol. 7 No. 4 (2020)

Section

Original Articles

License

Copyright (c) 2020 Victor A Marchenko, Salavat S Khalikov, Yury A Vasilenko, Mikhail M Ilyin, Irina A Kravchenko

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Authors who publish with this journal agree to the following terms:

Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.

Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgement of its initial publication in this journal.

Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).