British Journal of Anaesthesia, 1988, Vol. 61, No. 5 569-574
© 1988 The Board of Management and Trustees of the British Journal of Anaesthesia
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RELATIVE BIOAVAILABILITY OF CONTROLLED RELEASE MORPHINE TABLETS (MST CONTINUS) IN CANCER PATIENTS
Continuing Care Unit, Royal Marsden Hospital Fulham Road, London SW3 6JJ
Department of Clinical Pharmacology, St Bartholomew's Hospital Medical College London
Department of Biochemistry, University of Surrey Guildford, Surrey
Correspondence to G. W. Hanks.
The bioavailability of oral controlled release morphine tablets (MST, Napp Laboratories) and oral morphine sulphate in aqueous solution (MSS) was compared in 10 patients with advanced cancer. Serum samples were analysed for morphine, morphine-3-glucuronide (M3G) and morphine-6-glucuronide (M6G) using a specific HPLC assay. The relative bioavailability of morphine with MST was significantly less than that with MSS (mean 80%, range 50110%) although there was no difference between the formulations in the relative availability of M3G and M6G. There was no significant difference between the formulations in the serum concentration of morphine at 12 h. The mean ratios morphine: M6G: M3G (comparing areas under the serum concentration-time curves) were 1:9:56. There was a highly significant linear relationship between the dose administered and AUC for morphine, M3G and M6G after MSS; and for morphine after MST. Median tmax for morphine was 0.5 h with MSS and 2.5h with MST; for M3G 1.5h with MSS and 3.0h with MST; and for M6G 1.5h with MSS and 3.25h with MST. A secondary peak of unconjugated morphine, which may represent enterohepatic circulation, was seen in several patients 24h after administration of elixir and 46 h after administration of MST.
*Institut Gustave-Roussy, rue Camille Desmoulins, 94805 Villejuif Cedex, France.
**Leeds General Infirmary, Leeds LS1 3EX.
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