Literature DB >> 1149487

Meptazinol (Wy 22811), a new analgesic: preliminary pharmacokinetic data.

M T Rosseel, M G Bogaert, F M Belpaire.   

Abstract

The authors report on the pharmacokinetic profile of a new analgesic, meptazinol, from studies of plasma and urine levels after intravenous injection in 4 healthy volunteers. Conjugated product is formed very soon after injection and its concentration changes little over the period studied compared with the unchanged product where a fast, then a relatively slow phase of decline can easily be distinguished, suggesting a two compartment open system model. Meptazinol is predominantly eliminated in this conjugated form by urinary excretion of the metabolites. Excretion is very rapid in the first few hours after dosing and elimination is almost completed after 24 hours.

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Year:  1975        PMID: 1149487     DOI: 10.1185/03007997509113668

Source DB:  PubMed          Journal:  Curr Med Res Opin        ISSN: 0300-7995            Impact factor:   2.580


  5 in total

1.  Studies on the absorption and disposition of meptazinol following rectal administration.

Authors:  R A Franklin; P J Southgate; A J Coleman
Journal:  Br J Clin Pharmacol       Date:  1977-04       Impact factor: 4.335

2.  Preliminary studies on the disposition of meptazinol in the neonate.

Authors:  R A Franklin; T Frost; P J Robson; M B Jackson
Journal:  Br J Clin Pharmacol       Date:  1981-07       Impact factor: 4.335

3.  Pharmacokinetics of meptazinol in man following repeated intramuscular administration.

Authors:  G Davies; A J Sinclair; S J Warrington; R Franklin; T Frost; A Latham; P J Robson
Journal:  Eur J Clin Pharmacol       Date:  1982       Impact factor: 2.953

Review 4.  Meptazinol. A review of its pharmacodynamic and pharmacokinetic properties and therapeutic efficacy.

Authors:  B Holmes; A Ward
Journal:  Drugs       Date:  1985-10       Impact factor: 9.546

5.  The disposition of meptazinol after single and multiple intravenous administration to pregnant and non-pregnant women.

Authors:  G R Murray; D Evans; T Lind; R A Franklin; D F Graham
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

  5 in total

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