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The absorption and elimination of ICI 74917 in man.

机译:ICI 74917在人体中的吸收和消除。

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摘要

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.
机译:1在哮喘患者和正常志愿者中均研究了ICI 74,917的药代动力学。 2通过从气雾剂和支气管镜吸入,以及通过静脉内,口服和颊途径将The化的化合物给药至肺。测量血浆,尿液,粪便,痰液和呼出空气中的放射性。 3支气管镜给药后,可吸收剂量的63%被吸收;气雾剂给药后,从肺中吸收了8%,并且吞咽了50%以上。 5静脉研究表明,药物以2:1的比例排入胆汁和尿液。 5最小的口腔吸收,没有颊吸收。 6没有evidence交换或药物代谢的证据。 7所有途径给药后的平均终末半衰期为16.1小时。然而,大部分剂量被迅速排泄。 8气雾剂给药是ICI 74,917临床应用的首选方法。

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