α二酮和米那克龙的药代动力学。

J W Sear, C Prys-Roberts
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引用次数: 0

摘要

对20例患者连续输注Althesin (alphaxalone: alphadolone acetate)和新型水溶性类固醇静脉麻醉剂minaxolone补充氧化亚氮氧麻醉。在输注期间和停止后的血液样本中估计血浆药物浓度。两组(阿司松:n = 11,米纳洛酮:n = 9)均未见血浆内药物蓄积的迹象。输注后血浆药物浓度的衰减可拟合为双指数方程,表明类固醇按开放的双室药代动力学模型分布。服用米纳洛酮后恢复时间较长可能与其水溶性有关,也与药物分布体积较大有关。气相色谱:质谱分析血液和尿液样本的研究证实,Althesin和minaloxone都在体内进行生物转化。肝与葡萄糖醛酸结合在亲脂剂Althesin的排泄中起重要作用。
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Alphadione and minaxolone pharmacokinetics.

Althesin (alphaxalone: alphadolone acetate) and the new water-soluble steroid intravenous anaesthetic agent minaxolone have been administered by continuous infusion to supplement nitrous oxide: oxygen anaesthesia in 20 patients. Plasma drug concentrations were estimated in blood samples taken during and following cessation of the infusion. In both group (Althesin: n = 11, minaxolone: n = 9), there was no evidence of drug accumulation within the plasma. The decay in the plasma drug concentrations after the infusion could be fitted to a bi-exponential equation, indicating that the steroids were distributed according to an open two-compartment pharmacokinetic model. The prolonged recovery following minaxolone may be related to its water-solubility, and to a larger volume of distribution of the drug. Studies gas chromatography: mass spectrometry to analyse samples of blood and urine have confirmed than Althesin and minaloxone both undergo biotransformation in the body. Hepatic conjugation to glucuronic acid is of importance in the excretion of the lipophilic agent, Althesin.

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