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ICI 74,917在人体中的吸收与消除。

The absorption and elimination of ICI 74,917 in man.

作者信息

Pickup M E, Johnson A J, May C S, Paterson J W, Harrison M P

出版信息

Br J Clin Pharmacol. 1977 Jun;4(3):357-66. doi: 10.1111/j.1365-2125.1977.tb00724.x.

Abstract

1 The pharmacokinetics of ICI 74,917 were studied in both asthmatic patients and normal volunteers. 2 The tritiated compound was administered to the lungs by inhalation from an aerosol and a bronchoscope, and by intravenous, oral and buccal routes. Radioactivity was measured in plasma, urine, faeces, sputum and exhaled air. 3 After bronchoscopic administration 63% of the available dose was absorbed; after aerosol administration 8% was absorbed from the lung and more than 50% swallowed. 5 Intravenous studies indicated that the drug is excreted in the bile and urine in the ratio 2:1. 5 Minimal oral and no buccal absorption occurred. 6 There was no evidence of tritium exchange or drug metabolism. 7 The mean terminal half-life following administration by all route was 16.1 hours. However, the majority of the dose was rapidly excreted. 8 Aerosol administration is the method of choice for the clinical use of ICI 74,917.

摘要
  1. 对ICI 74,917在哮喘患者和正常志愿者体内的药代动力学进行了研究。2. 用氚标记的化合物通过气雾剂和支气管镜经吸入方式给药至肺部,同时也采用静脉、口服和颊部给药途径。对血浆、尿液、粪便、痰液和呼出气体中的放射性进行了测量。3. 经支气管镜给药后,63%的可用剂量被吸收;经气雾剂给药后,8%从肺部吸收,超过50%被吞咽。5. 静脉给药研究表明,该药物经胆汁和尿液排泄的比例为2:1。5. 口服吸收极少,颊部无吸收。6. 没有氚交换或药物代谢的证据。7. 所有给药途径后的平均终末半衰期为16.1小时。然而,大部分剂量迅速排泄。8. 气雾剂给药是ICI 74,917临床应用的首选方法。

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