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J Clin Pharmacol ; 44(3): 293-304, 2004 Mar.
Article in English | MEDLINE | ID: mdl-14973306

ABSTRACT

Twelve methadone-maintained HIV-negative subjects were given saquinavir/ritonavir (SQV/rtv) 1600 mg/100 mg once daily for 14 days. Pharmacokinetic evaluations of total and unbound methadone enantiomers (R and S) were conducted before and after SQV/rtv. SQV/rtv was well tolerated, with no ACTG Grade 3-4 adverse events, no evidence of sedation, and no changes in methadone dose. For R-methadone (active isomer), C(max), AUC(0-24 h), and C(min) were unchanged, but percent unbound 4 hours after dosing was reduced by 12%. For S-methadone, no differences in pharmacokinetic parameters of total drug were seen, but unbound concentrations were reduced by 15% and 21% at 4 and 24 hours after dosing, respectively. SQV trough concentrations exceeded the anticipated EC(50) (50 ng/mL) in 10/12 subjects, persisting for at least 6 hours after the final dose in 4/6 subjects. Once-daily SQV/rtv in methadone-maintained subjects is safe and not associated with any clinically significant interaction with methadone during 14 days of concomitant administration.


Subject(s)
HIV Protease Inhibitors/pharmacology , Methadone/pharmacokinetics , Narcotics/pharmacokinetics , Ritonavir/pharmacology , Saquinavir/pharmacology , Adult , Chromatography, Liquid , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Interactions , HIV Protease Inhibitors/blood , Humans , Male , Mass Spectrometry , Metabolic Clearance Rate , Methadone/blood , Methadone/chemistry , Middle Aged , Narcotics/blood , Narcotics/chemistry , Ritonavir/blood , Saquinavir/blood , Stereoisomerism , Time Factors
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