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3-脱氮鸟嘌呤的临床药代动力学

Clinical pharmacokinetics of 3-deazaguanine.

作者信息

Pendyala L, Creaven P J, Whitfield L R

机构信息

Dept. of Medicine, Roswell Park Cancer Institute, Buffalo, NY 14263.

出版信息

Cancer Chemother Pharmacol. 1991;29(1):33-6. doi: 10.1007/BF00686333.

Abstract

3-Deazaguanine (3DG), an antipurine antimetabolite, has recently completed a phase I clinical trial at this Institute. The drug was given on a daily x 5 schedule by i.v. infusion over 0.25-2.16 h. The pharmacokinetics of 3DG during 16 courses were studied in 12 patients at doses of 200-800 mg/m2. 3DG in plasma was measured by an isocratic reverse-phase high-performance liquid chromatographic (HPLC) procedure carried out on IBM phenyl columns at 40 degrees C using 10 mM phosphate buffer (pH 7) as the mobile phase and detection at 300 nm. Plasma decay of 3DG was biexponential in all patients. The AUC correlated linearly with dose at 200-600 mg/m2 but deviated from linearity at doses greater than 600 mg/m2. The drug was cleared rapidly from plasma; at doses of 200-600 mg/m2, the mean plasma clearance was 61.64 +/- 9.97 l/h and the mean terminal-phase elimination half-life was 1.6 +/- 0.6 h. The steady-state volume of distribution (98.9 +/- 29.1 l) and distribution coefficient (1.24 +/- 0.39 l/kg) indicated extensive tissue distribution for the drug. No statistically significant difference was observed between the pharmacokinetics of 3DG on day 1 and that on day 4 as evaluated in three patients for whom complete plasma data were available on both days.

摘要

3-去氮鸟嘌呤(3DG),一种抗嘌呤抗代谢物,最近在本研究所完成了一项I期临床试验。该药物采用每日静脉输注5天的给药方案,输注时间为0.25至2.16小时。在12名患者中,以200 - 800mg/m²的剂量研究了16个疗程中3DG的药代动力学。血浆中的3DG通过等度反相高效液相色谱(HPLC)法测定,该方法在40℃的IBM苯基柱上进行,使用10mM磷酸盐缓冲液(pH 7)作为流动相,并在300nm处进行检测。所有患者中3DG的血浆衰减均为双指数形式。在200 - 600mg/m²剂量下,AUC与剂量呈线性相关,但在剂量大于600mg/m²时偏离线性。药物从血浆中迅速清除;在200 - 600mg/m²剂量下,平均血浆清除率为61.64±9.97l/h,平均终末相消除半衰期为1.6±0.6小时。稳态分布容积(98.9±29.1l)和分布系数(1.24±0.39l/kg)表明该药物在组织中分布广泛。在3名两天均有完整血浆数据的患者中评估发现,3DG在第1天和第4天的药代动力学之间未观察到统计学上的显著差异。

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