Pharmacokinetics of Single Intravenous and Oral Doses of Dolasetron Mesylate in Healthy Elderly Volunteers
| Autor: | Hélène Landriault, Ellen Dempsey, Stéphane Bourque, Jean Spénard |
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| Rok vydání: | 1996 |
| Předmět: |
Indoles
Metabolic Clearance Rate medicine.drug_class Metabolite Biological Availability Urine Pharmacology Statistics Nonparametric chemistry.chemical_compound Pharmacokinetics Oral administration medicine Humans Antiemetic Pharmacology (medical) Dolasetron Chromatography High Pressure Liquid Aged Volume of distribution Cross-Over Studies business.industry Primary metabolite chemistry Antiemetics business Quinolizines medicine.drug |
| Zdroj: | The Journal of Clinical Pharmacology. 36:903-910 |
| ISSN: | 0091-2700 |
| DOI: | 10.1002/j.1552-4604.1996.tb04757.x |
| Popis: | Dolasetron mesylate (MDL 73,147EF, Anzemet; Hoechst Marion Roussel, Laval, Canada) is a 5-HT3 receptor antagonist undergoing clinical evaluation for use as an antiemetic agent. The pharmacokinetics of dolasetron and its reduced metabolite (MDL 74,156) were studied after administration of single intravenous and oral doses of dolasetron mesylate 2.4 mg/kg in 18 healthy elderly subjects. Expressed as the dolasetron base, this dose was 1.8 mg/kg. Dolasetron was rapidly metabolized to the reduced metabolite, which appeared in plasma within 10 minutes after intravenous or oral administration. The mean half-life (t1/2) of dolasetron was 0.24 hours after intravenous administration and 0.50 hours after oral administration. The pharmacokinetic parameters of the reduced metabolite were similar after intravenous and oral administration. The apparent absolute bioavailability of the reduced metabolite was 89%, and it had an elimination t1/2 of approximately 7 hours and an apparent volume of distribution (Vd beta) of 4.69 L/kg. Dolasetron was not detected in urine. Metabolites were excreted in urine almost completely within 24 hours of administration. The primary metabolite detected in urine was the (+)-enantiomer of the reduced metabolite, which accounted for 25.35% (+/- 7.79%) and 18.88% (+/- 7.65%) of the intravenous and oral doses, respectively. Hydroxylated metabolites accounted for 5% or less of the total dose via either route. The pharmacokinetics of the reduced metabolite after single intravenous or oral doses in elderly volunteers were consistent with pharmacokinetics observed in both young healthy men and cancer patients receiving high-dose cisplatin chemotherapy. Dosage adjustments of dolasetron mesylate on the basis of age do not appear to be necessary. |
| Databáze: | OpenAIRE |
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