STUDY OF ACUTE TOXICITY AND ANTITUMOR ACTIVITY OF NEW COLCHAMETIN PREPARATION СOLCHAMETIN

Yuldashev Javlonabduraimovich, Ibragimov Shavkat Narzikulovich, Shakhanova Shakhnoza Shavkatovna, Esankulova Bustonoy Sobirovna
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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 202g. both sexes and 60 male and female rats weighing 14010g 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.
新型秋黄素制剂的急性毒性及抗肿瘤活性研究Сolchametin
研究了一种新型抗肿瘤制剂“秋黄素”(K-2)在不同给药方式下对小鼠和大鼠的急性毒性及其对2种肿瘤菌株的抗肿瘤活性。根据Litchfield和Wilcoxon方法,对体重202g的白色不育小鼠60只进行了单次腹腔给药的急性毒性试验。雌雄大鼠各60只,体重14010g,每组5只,小鼠、大鼠共120只。12只非生育小鼠和16只直系小鼠输注肿瘤S-180和ACATON,在肿瘤输注10次后第4天注射该制剂,研究其抗肿瘤活性。按照抑制肿瘤生长(SRW)、动物体重和脾脏的标准进行评价。p < 0.05被认为是可靠的。结果。对小鼠进行单次营养诱导,获得了上述数据:LD50使的平均致死剂量890毫克/公斤(-150 + 172),在口腔医学介绍K-2老鼠的LD50等于3250毫克/公斤(-630 + 650),在单一vnutribryushinny LD50老鼠药K-2 LD50使410(-56 + 61)毫克/公斤,LD50单一口头介绍老鼠使3250毫克/公斤(-630 + 650),定义同样的方法引入LD10, LD16 LD84价值的抗肿瘤活性药物的肿瘤株K-2 99/90%肉瘤180高。对于ACATON肿瘤,腹腔给药时K-2效应较低,达到76/75%,但对两种肿瘤的作用均伴有造血指标的降低。结论。对制剂K-2所含物质的急性毒性研究表明,该制剂属于ⅳ类低毒化合物。在2例肿瘤中,新药疗效高,但造血指标降低。
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