{"title":"STUDY OF ACUTE TOXICITY AND ANTITUMOR ACTIVITY OF NEW COLCHAMETIN PREPARATION СOLCHAMETIN","authors":"Yuldashev Javlonabduraimovich, Ibragimov Shavkat Narzikulovich, Shakhanova Shakhnoza Shavkatovna, Esankulova Bustonoy Sobirovna","doi":"10.37547/ijmscr/volume03issue03-05","DOIUrl":null,"url":null,"abstract":"The aim of the study was to study acute toxicity in different methods of administration in mice and rats of a new antitumor preparation \"colchametin\" (K-2) and its antitumor activity on 2 strains of tumors Material and research methods. Acute toxicity of the preparation K-2 with a single intraperitoneal administration was carried out according to the Litchfield and Wilcoxon method in 60 white infertile mice weighing 202g. both sexes and 60 male and female rats weighing 14010g 5 animals in each group, a total of 120 mice and rats were used. The study of antithumor activity was performed on 12 non-fertile and 16 linear mice with transfused tumors S-180 and ACATON, which was injected with preparations on the 4th day after tumour was administered on day 4 after tumour transfusion 10 times. Evaluation of the results was carried out according to standard criteria: inhibition of tumor growth (SRW), body weight and spleen of animals. Differences at p < 0.05 were considered reliable. Results. Such data at single vnutribryushinny introduction are obtained to mice: the average lethal dose of LD50 makes 890 (-150+172) mg/kg, At oral introduction of medicine K-2 to mice of LD50 is equal to 3250 (-630+650) mg/kg, LD50 at single vnutribryushinny to rats of medicine K-2 LD50 makes 410 (-56+61) mg/kg, LD50 at single oral introduction to rats makes 3250 (-630+650) mg/kg, are defined also at all ways of introduction of LD10, LD16 and LD84 value The antitumor activity of the drug K-2 on the tumor strain of Sarcoma 180 was high - about 99/90%. On the ACATON tumor, the K-2 effect during intraperitoneal administration was lower and reached 76/75%, however, its effect on both tumors was accompanied by a decrease in hematopoietic indicators. Conclusions. The study of the acute toxicity of the substance of the preparation K-2 showed that this preparation belongs to class IV of low-toxic compounds. On 2 tumors, the effect of the new drug was high, but hematopoietic indicators were reduced.","PeriodicalId":297181,"journal":{"name":"International Journal of Medical Sciences And Clinical Research","volume":"96 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Medical Sciences And Clinical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37547/ijmscr/volume03issue03-05","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The aim of the study was to study acute toxicity in different methods of administration in mice and rats of a new antitumor preparation "colchametin" (K-2) and its antitumor activity on 2 strains of tumors Material and research methods. Acute toxicity of the preparation K-2 with a single intraperitoneal administration was carried out according to the Litchfield and Wilcoxon method in 60 white infertile mice weighing 202g. both sexes and 60 male and female rats weighing 14010g 5 animals in each group, a total of 120 mice and rats were used. The study of antithumor activity was performed on 12 non-fertile and 16 linear mice with transfused tumors S-180 and ACATON, which was injected with preparations on the 4th day after tumour was administered on day 4 after tumour transfusion 10 times. Evaluation of the results was carried out according to standard criteria: inhibition of tumor growth (SRW), body weight and spleen of animals. Differences at p < 0.05 were considered reliable. Results. Such data at single vnutribryushinny introduction are obtained to mice: the average lethal dose of LD50 makes 890 (-150+172) mg/kg, At oral introduction of medicine K-2 to mice of LD50 is equal to 3250 (-630+650) mg/kg, LD50 at single vnutribryushinny to rats of medicine K-2 LD50 makes 410 (-56+61) mg/kg, LD50 at single oral introduction to rats makes 3250 (-630+650) mg/kg, are defined also at all ways of introduction of LD10, LD16 and LD84 value The antitumor activity of the drug K-2 on the tumor strain of Sarcoma 180 was high - about 99/90%. On the ACATON tumor, the K-2 effect during intraperitoneal administration was lower and reached 76/75%, however, its effect on both tumors was accompanied by a decrease in hematopoietic indicators. Conclusions. The study of the acute toxicity of the substance of the preparation K-2 showed that this preparation belongs to class IV of low-toxic compounds. On 2 tumors, the effect of the new drug was high, but hematopoietic indicators were reduced.