Pharmacokinetics of codeine and its metabolites in Caucasian healthy volunteers: comparisons between extensive and poor hydroxylators of debrisoquine.
- 1 June 1991
- journal article
- research article
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 31 (6), 635-642
- https://doi.org/10.1111/j.1365-2125.1991.tb05585.x
Abstract
1. The kinetics of codeine and seven of its metabolites codeine‐6‐ glucuronide (C6G), norcodeine (NC), NC‐glucuronide (NCG), morphine (M), M‐3 (M3G) and 6‐glucuronides (M6G), and normorphine (NM) were investigated after a single oral dose of 50 mg codeine phosphate in 14 healthy Caucasian subjects including eight extensive (EM) and six poor (PM) hydroxylators of debrisoquine. The plasma and urine concentrations of codeine and the metabolites were measured by h.p.l.c. 2. The mean area under the curve (AUC), half‐life and total plasma clearance of codeine were 1020 +/‐ 340 nmol l‐1 h, 2.58 +/‐ 0.57 h and 2.02 +/‐ 0.73 l h‐1 kg‐1, respectively. There were no significant differences between EM and PM in these aspects. 3. PM had significantly lower AUC of M3G, the active metabolites M6G, NM and M (P less than 0.0001), and lower partial metabolic clearance by O‐demethylation (P less than 0.0001). In contrast, the PM had higher AUC of NC (P less than 0.05) than the EM. There was no difference between PM and EM in the AUC of C6G and NCG, nor in the partial clearances by N‐demethylation and glucuronidation. 4. Among EM, the AUC of C6G was 15 times higher than that of codeine, which in turn was 50 times higher than that of M. The AUCs of M6G and NM were about 6 and 10 times higher than that of M, respectively. The partial clearance by glucuronidation was about 8 and 12 times higher than those by N‐ and O‐demethylations, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)Keywords
This publication has 36 references indexed in Scilit:
- Morphine-6-glucuronide: Analgesic effects and receptor binding profile in ratsLife Sciences, 1988
- POLYMORPHIC O-DEMETHYLATION OF CODEINEThe Lancet, 1988
- Bioactivation of the narcotic drug codeine in human liver is mediated by the polymorphic monooxygenase catalyzing debrisoquine 4-hydroxylation (cytochrome P-450 dbl/bufI)Biochemical and Biophysical Research Communications, 1988
- ANALGESIC ACTIVITY OF MORPHINE-6-GLUCURONIDEThe Lancet, 1988
- Pharmacokinetics of Codeine After Single-and Multiple-Oral-Dose Administration to Normal VolunteersThe Journal of Clinical Pharmacology, 1987
- POTENTIAL ANALGESIC CONTRIBUTION FROM MORPHINE-6-GLUCURONIDE IN CSFThe Lancet, 1987
- Oral Administration of Codeine in the Presence of Ethanol: A Pharmacokinetic Study in ManBasic & Clinical Pharmacology & Toxicology, 1987
- High-Dose Morphine and Methadone in Cancer PatientsClinical Pharmacokinetics, 1986
- MORPHINE-6-GLUCURONIDE, AN IMPORTANT METABOLITEThe Lancet, 1985
- Patient-controlled Analgesic Therapy, Part IVClinical Pharmacokinetics, 1982