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~3H-咯萘啶在小鼠体内的分布和排泄

DISTRIBUTION AND EXCRETION OF ~3H-PYRONARIDINE IN MICE

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【作者】 冯正吴祖帆王翠英江善根

【Author】 Z Feng, ZF Wu, CY Wang and AG Jiang~* (Institute of Parasitic Diseases, Chinese Academy of Preventive Medicine, Shanghai; ~*Shanghai Institute of Nuclear Research, Academia Sinica Shanghai)

【机构】 中国预防医学科学院寄生虫病研究所中国科学院上海原子核研究所 上海上海上海

【摘要】 <正> 咯萘啶(PND)是一种疟原虫红内期裂殖体杀灭剂,与氯喹无交叉抗性,对恶性疟和间日疟均有显著疗效。用家兔的初步实验表明,PND原药在尿中的排泄量仅约为剂量的2%。我们已报告该药在体内分布较广。文献报道PND对鼠疟原虫红内期裂殖体有长效作用。为进一步了解该药的体内过程,对~3H-PND在小鼠体内的分布和排泄进行了研究。

【Abstract】 The distribution of ~3H in selected tissues was studied after intragastric (ig) or intraperitoneal (ip) administration of ~3H-pyronaridine 30 mg/kg to mice. The major sites of distribution of pyronaridine (PND)-derived radioactivity were the liver, small intestine and its-content, large intestine and its content, kidneys, lungs and stomach. Twenty four hours after ig, 18% of the dose was found in the liver, 12% in residual carcasses, and 54% was excreted via the urine and feces. In the case of ip, 20% of the dose was present in the liver, 20% in residual carcasses ard about 40% was excreted in the urine and feces. About 20% of the dose was detected in the urine, and 34~40% was recovered from the feces during the period of 0~96 h. After then, ~3H was excreted slowly. The total urinary excretion during 12 days after ig and ip was 20.83 and 24.07% of the dose, and the total fecal excretion, 40.44 and 41.24%, respectively. The slow excretion may explain the fact that pyronardine showed a residual blood schizontocidal activity in mice infected with Plasmodium yoelii.

【关键词】 抗疟药咯萘啶
【Key words】 Antimalarial drugPyronaridine
  • 【文献出处】 药学学报 ,Acta Pharmaceutica Sinica , 编辑部邮箱 ,1988年08期
  • 【被引频次】2
  • 【下载频次】25
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