Literature DB >> 11745739

Limited phase I study of morphine-3-glucuronide.

R T Penson1, S P Joel, S Clark, A Gloyne, M L Slevin.   

Abstract

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) etamolL(-1) x 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). Copyright 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association

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Year:  2001        PMID: 11745739     DOI: 10.1002/jps.1131

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  17 in total

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4.  Morphine metabolite pharmacokinetics during venoarterial extra corporeal membrane oxygenation in neonates.

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5.  Cyclosporine-inhibitable blood-brain barrier drug transport influences clinical morphine pharmacodynamics.

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6.  Heroin-using drivers: importance of morphine and morphine-6-glucuronide on late clinical impairment.

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7.  The pharmacokinetics of codeine and its metabolites in Blacks with sickle cell disease.

Authors:  Stacy S Shord; Larisa H Cavallari; Weihua Gao; Hyun-Young Jeong; Kelly Deyo; Shitalben R Patel; Joseph R Camp; Susan M Labott; Robert E Molokie
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8.  Differential in vitro inhibition of M3G and M6G formation from morphine by (R)- and (S)-methadone and structurally related opioids.

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9.  Pharmacokinetic modelling of morphine, morphine-3-glucuronide and morphine-6-glucuronide in plasma and cerebrospinal fluid of neurosurgical patients after short-term infusion of morphine.

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10.  A novel metabolic pathway of morphine: formation of morphine glucosides in cancer patients.

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Journal:  Br J Clin Pharmacol       Date:  2003-06       Impact factor: 4.335

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