Limited phase I study of morphine-3-glucuronide

被引:9
作者
Penson, RT
Joel, SP
Clark, S
Gloyne, A
Slevin, ML
机构
[1] Massachusetts Gen Hosp, Div Hematol Oncol, Boston, MA 02114 USA
[2] St Bartholomews Hosp, Dept Med Oncol, London EC1A 7BE, England
关键词
morphine; morphine-3-glucuronide; toxicity; pharmacokinetics;
D O I
10.1002/jps.1131.abs
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The toxicity of morphine-3-glucuronide (M3G) has been investigated in an open, uncontrolled, single-blinded, single dose study over a limited range of doses. Three cohorts each of three healthy volunteers received 7.5, 15, and 30 mg/70 kg intravenous (IV) M3G. Blood sampling was undertaken for the following 24 h. Subjective toxicity was recorded on visual analogue scales and plasma M3G concentrations measured by a specific HPLC assay. Virtually no effects and no change in cardiovascular or respiratory parameters were seen. The pharmacokinetics fitted a two-compartment model. The mean elimination half-life (+/-S.D.) of M3G was 1.66 (+/-0.47) h. Mean AUC standardized to a dose of 1 mg/70 kg was 228 (+/- 62) eta molL(-1).h. Mean M3G clearance was 169 (+/- 48) mLmin(-1) and the mean volume of distribution was 23.1 (+/-4.8) liters. At the doses investigated there were no clear neuroexcitatory effects, no opioid effects, and the pharmacokinetics were very similar to those of morphine-6-glucuronide (M6G). (C) 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association.
引用
收藏
页码:1810 / 1816
页数:7
相关论文
共 32 条