Preview

Russian Journal of Parasitology

Advanced search

Subchronic toxicity of a drug based on D-cyphenothrin, pyriproxyfen and piperonyl butoxide

https://doi.org/10.31016/1998-8435-2024-18-4-419-426

Abstract

The purpose of the research is to study the effects of a combined drug based on D-cyphenothrin, pyriproxyfen and piperonyl butoxide on the body of rats with repeated dermal application in a subchronic experiment.
Materials and methods. The drug subchronic toxicity was studied in the vivarium of the VNIIP – FSC VIEV on 30 male rats divided into one control and two experimental groups of 10 animals each. The drug was applied daily for 7 days to the experimental rats at doses of 1/10 and 1/20 of the maximum possible dose for dermal application determined in an acute experiment when studying LD50. On the first day and at 10 days after the last application of the drug, half of the animals from each group were euthanized and blood samples were taken to determine morphological and biochemical parameters. A macroscopic examination of the organs was carried out; their mass was determined, and mass coefficients were calculated.
Results and discussion. The drug based on D-cyphenothrin, pyriproxyfen and piperonyl butoxide applied dermally for 7 days in doses of 1/10 of LD50 (3071 mg/kg) and 1/20 of LD50 (1535.5 mg/kg) had no negative effect on the rats' organism, or its physiological state, and caused no changes in the morphological or biochemical blood parameters, as well as the mass coefficients of the internal organs. Doses of 3071 and 1535.5 mg/kg were inactive (safe). The threshold and toxic doses could not be determined

About the Authors

M. V. Arisov
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” (VNIIP – FSC VIEV)
Russian Federation

Mikhail V. Arisov, Doctor of Veterinary Sciences, Professor of the Russian Academy of Sciences, Head of the Laboratory of Ectoparasitosis, Head

Researcher ID: B-7834-2018, Scopus ID: 57207942094

Moscow



D. S. Poselov
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” (VNIIP – FSC VIEV)
Russian Federation

Dmitry S. Poselov, Candidate of Veterinary Sciences, Senior Researcher 

Researcher ID: U-6241-2018 

Moscow



E. V. Poselova
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” (VNIIP – FSC VIEV)
Russian Federation

Ekaterina V. Poselova, Candidate of Veterinary Sciences, Senior Researcher 

Researcher ID: AAI-4469-2021 

Moscow



A. A. Stepanov
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” (VNIIP – FSC VIEV)
Russian Federation

Alexey A. Stepanov, Candidate of Veterinary Sciences 

Researcher ID: U-8135-2018 

Moscow



T. S. Novik
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” (VNIIP – FSC VIEV)
Russian Federation

Novik Tamara S., Doctor of Biological Sciences, Professor of the Laboratory of Experimental Therapy 

Researcher ID: U-6372-2018, Scopus ID: 6601960888 

Moscow



References

1. Biryukova N. P., Rusakov S.V., Napalkova V.V. General principles of preclinical safety evaluation of pharmacological drugs for veterinary use. Veterinarnyy vrach = Veterinary Doctor. 2018; 1: 3-9. (In Russ.)

2. Burmistrova M. I., Vasilevich F. I., Deltsov A. A. Effects of the insectoacaricidal drug Delcid 7.5® on the rabbits’ organism. Veterinariya i kormleniye = Veterinary medicine and feeding. 2021; 2: 10- 12. (In Russ.) https://doi.org/10.30917/ATTVK-1814-9588-2021-2-2

3. Vasiliev A. N. High-quality preclinical research is a necessary stage in new drug development and introduction into clinical practice. Antibiotiki i khimioterapiya = Antibiotics and chemotherapy. 2012; 57 (1-2): 41-49. (In Russ.)

4. Vasiliev A. N., Niyazov R. R., Gavrishina E. V., Dranitsyna M. A., Kulichev D. A. Problems of planning and performing preclinical studies in the Russian Federation. Remedium = Remedium. 2017; 9: 6-19. (In Russ.) https://doi.org/10.21518/1561-5936-2017-9-6-18

5. Islamov R. A. Methodology for an experiment using laboratory animals. Vestnik Kazakhskogo natsional'nogo meditsinskogo universiteta = Bulletin of the Kazakh National Medical University. 2016; 1: 522-525. (In Russ.)

6. Lipatov V. A., Kryukov A. A., Severinov D. A., Saakyan A. R. Ethical and legal aspects of in vivo experimental biomedical research, part I. Rossiyskiy mediko-biologicheskiy vestnik imeni akademika I. P. Pavlova = I. P. Pavlov Russian Medical Biological Herald. 2019; 27 (1): 80-92. (In Russ.) https://doi.org/10.23888/PAVLOVJ201927180-92

7. Lipatov V. A., Severinov D. A., Kryukov A. A., Saakyan A. R. Ethical and legal aspects of in vivo experimental biomedical research.Part II. Rossiyskiy mediko-biologicheskiy vestnik imeni akademika I. P. Pavlova = I. P. Pavlov Russian Medical Biological Herald. 2019; 27 (2): 245-257. (In Russ.) https://doi.org/10.23888/PAVLOVJ2019272245-257

8. Makhvatova N. V. Acute and subchronic toxicity of multicomponent antiparasitic drugs Insacar Total C Plus and Insacar Total K Plus. Rossiyskiy parazitologicheskiy zhurnal = Russian Journal of Parasitology. 2022; 16 (2): 193–202. (In Russ.). https://doi.org/10.31016/1998-8435-2022-16-2-193-202

9. Mironov A. N., Bunyatyan N. D., Vasiliev A. N., Verstakova O. L., Zhuravleva M. V., Lepakhin V. K., Korobov N. V., Merkulov V. A., Orekhov S. N., Sakaeva I. V., Uteshev D. B., Yavorsky A. N. Guidelines for drug preclinical studies. Part 1. M.: Grif i K, 2012; 944. (In Russ.)

10. Tochieva O. N., Arisov M. V. Toxicological evaluation of combination drugs based on imidacloprid, moxidectin and pyriproxyfen. Rossiyskiy parazitologicheskiy zhurnal = Russian Journal of Parasitology. 2024; 18 (3): 301–307. (In Russ.). https://doi.org/10.31016/1998-8435-2024-18-3-301-307

11. Tyurenkov I. N., Lomkina E. M., Kurkin D. V., Bakulin D. A., Volotova E. V. Ethical aspects of preclinical studies. Vedomosti Nauchnogo tsentra ekspertizy sredstv meditsinskogo primeneniya. Regulyatornyye issledovaniya i ekspertiza lekarstvennykh sredstv = Bulletin of the Scientific Center for Expert Evaluation of Medicinal Products. Regulatory studies and expert evaluation of medicinal products. 2015; 3: 36-41. (In Russ.)

12. Khabriev R. U. Guidelines for experimental (preclinical) study of new pharmacological substances. M.: Medicine, 2005; 832. (In Russ.)

13. Regulation (EU) No 528/2012 concerning the making available on the market and use of biocidal products. Evaluation of active substances. Assessment Report. Cyphenothrin Product-type 18 (insecticides, acaricides and products to control other arthropods). Greece, 2018; 87.


Review

For citations:


Arisov M.V., Poselov D.S., Poselova E.V., Stepanov A.A., Novik T.S. Subchronic toxicity of a drug based on D-cyphenothrin, pyriproxyfen and piperonyl butoxide. Russian Journal of Parasitology. 2024;18(4):419-426. (In Russ.) https://doi.org/10.31016/1998-8435-2024-18-4-419-426

Views: 1060


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


ISSN 1998-8435 (Print)
ISSN 2541-7843 (Online)