Acute oral and cutaneous toxicities of Cyflunit- flock tested on laboratory animals

Russian Journal of Parasitology, 2016, V.35, Iss.1
Received  26.11.2015
Accepted   19.01.2016
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ACUTE ORAL AND CUTANEOUS TOXICITIES OF CYFLUNIT- FLOCK TESTED ON LABORATORY ANIMALS

 

Glukhareva E.V.
All-Russian Scientific Research Institute of Fundamental and Applied Parasitology of Animals and Plants named after K.I. Skryabin, 117218, Moscow, 28 B. Cheremushkinskaya St., e-mail: vigis@ncport.ru

 

Abstract

Objective of research:  to determine the toxicological properties of the preparation Cyflunit- Flock under acute experimental conditions at oral and subcutaneous administration routes to laboratory animals.

Materials and methods:  White outbred mice and white outbred rats of both genders were used for testing. Each dose of the preparation was tested on groups of males and females to identify the eventual sex differences in drug-responsiveness. In experiment on mice, animals were divided into 5 groups of 10 animals each. The medicine was given orally at the doses of 4350, 8700, 13050, 17400 and 21750 mg a.i./kg. In experiment on rats, 4 experimental male and 4 female groups were formed  (6 animals in each). The drug was given orally at the doses of 17400 and  21750, 26100 and  30450  mg a.i./kg.   While studying the acute cutaneous toxicity, Cyflunit- Flock was applied at the doses 870, 1740, 4350 and 8700 mg a.i./kg in 4 experimental groups of male and 4 groups of female rats of 6 animals each. Observations of general health status, behavior of animals, intoxication symptoms and eventual death of animals were conducted within 14 days.

Results and discussion:   LD50 of Cyflunit-Flock at oral administration to mice of both genders was 12180 mg/kg, at oral administration to male rats - 22475 mg/kg, to female rats - 23925 mg/kg. At cutaneous use of the preparation in rats, LD50 was more than 8700 mg/kg.
According to the standard hygienic classification, the preparation belongs to the 4th hazard  class (low-hazard substances)

Keywords:  toxicity, LD50, Cyflunit- Flock, cyfluthrin, mice, rats.

References

1. Rukovodstvo po eksperimental'nomu (doklinicheskomu) izucheniyu novyh farmakologicheskih veshhestv [Handbook for experimental (pre-clinical) studies of new pharmaceutical substances]. M., Medizina, 2005. 832 p. (in Russian)

2. Mironov A. N., Bunatyan N. D. et al. Rukovodstvo po provedeniju doklinicheskih issledovaniy lekarstvennyh sredstv. Chast' pervaya [Handbook for conducting preclinical studies of new pharmaceutical substances]. M. 944 p. (in Russian)

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© 2015 The Author(s). Published by All-Russian Scientific Research Institute of  Fundamental and Applied Parasitology of Animals and Plants named after K.I. Skryabin. 
This is an open access article under the Agreement of 02.07.2014 (Russian Science Citation Index (RSCI)) and the Agreemnt of 12/06/2014 (CABI org / Human Sciences section)