Vatin A E, Filatov P P
Antibiotiki. 1975 Jan;20(1):6-11.
The pharmacokinetics of C14-olivomycin after its single intravenous administration to mice with lymphosarcome (LIO-I) was studied. It was shown that according to the specific radioactivity the organs may be placed in the following order: I hour after the antibiotic administration-the blood, liver, spleen, thymus, tumor, muscle; 3 hour after the administration-the liver, spleen, thymus, blood, tumor, muscle. Accumulation of olivomycin in the mouse organs was mainly in direct dependence on the dose of the antibiotic administered. Chromatography of the substances extraceted with ethylacetate from the urine collected at various periods after C14-olivomycin administration showed the presence of a new radioactive product (Rf 0.35-0.37) in addition to the unchanged antibiotic (Rf 0.53). Bioautographic analysis of the chromatograms showed that the product of C14-olivomycin conversion preserved its biological activity. The analysis of the substances extracted with ethylacetate from the liver, spleen and tumors 3 hours after the antibiotic administration reveiled (except of the liver) the presence of a spot with Rf corresponding to that of the initial drug.
研究了C14-橄榄霉素单次静脉注射给患有淋巴肉瘤(LIO-I)的小鼠后的药代动力学。结果表明,根据比放射性,各器官可按以下顺序排列:抗生素给药后1小时——血液、肝脏、脾脏、胸腺、肿瘤、肌肉;给药后3小时——肝脏、脾脏、胸腺、血液、肿瘤、肌肉。橄榄霉素在小鼠器官中的蓄积主要直接取决于所给抗生素的剂量。对C14-橄榄霉素给药后不同时间段收集的尿液用乙酸乙酯萃取的物质进行色谱分析,结果显示除了未变化的抗生素(比移值0.53)外,还存在一种新的放射性产物(比移值0.35 - 0.37)。对色谱图的生物自显影分析表明,C14-橄榄霉素转化产物保留了其生物活性。抗生素给药3小时后,对从肝脏、脾脏和肿瘤中用乙酸乙酯萃取的物质进行分析发现(肝脏除外),存在一个比移值与初始药物相对应的斑点。