新型秋黄素制剂的急性毒性及抗肿瘤活性研究Сolchametin

Yuldashev Javlonabduraimovich, Ibragimov Shavkat Narzikulovich, Shakhanova Shakhnoza Shavkatovna, Esankulova Bustonoy Sobirovna
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引用次数: 0

摘要

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
STUDY OF ACUTE TOXICITY AND ANTITUMOR ACTIVITY OF NEW COLCHAMETIN PREPARATION СOLCHAMETIN
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.
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