Mechanism-based PK/PD Modeling of the Respiratory Depressant Effect of Buprenorphine and Fentanyl in Healthy Volunteers
Autor: | Meindert Danhof, Raymonda Romberg, Ashraf Yassen, Erik Olofsen, Albert Dahan, Luc J. Teppema, Elise Sarton |
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Rok vydání: | 2007 |
Předmět: |
Adult
Male Agonist Metabolic Clearance Rate medicine.drug_class Pharmacology Models Biological Fentanyl Double-Blind Method Pharmacokinetics medicine Humans Pharmacology (medical) Respiratory system PK/PD models Chemistry Half-life Buprenorphine Analgesics Opioid Anesthesia Pharmacodynamics Female Respiratory Insufficiency Half-Life medicine.drug |
Zdroj: | Clinical Pharmacology & Therapeutics. 81:50-58 |
ISSN: | 1532-6535 0009-9236 |
DOI: | 10.1038/sj.clpt.6100025 |
Popis: | The objective of this study was to characterize the pharmacokinetic/pharmacodynamic (PK/PD) relationship of buprenorphine and fentanyl for the respiratory depressant effect in healthy volunteers. Data on the time course of the ventilatory response at a fixed P(ET)CO(2) of 50 mm Hg and P(ET)O(2) of 110 mm Hg following intravenous administration of buprenorphine and fentanyl were obtained from two phase I studies (50 volunteers received buprenorphine: 0.05-0.6 mg/70 kg and 24 volunteers received fentanyl: 0.075-0.5 mg/70 kg). The PK/PD correlations were analyzed using nonlinear mixed effects modeling. A two- and three-compartment pharmacokinetic model characterized the time course of fentanyl and buprenorphine concentration, respectively. Three structurally different PK/PD models were evaluated for their appropriateness to describe the time course of respiratory depression: (1) a biophase distribution model with a fractional sigmoid E(max) pharmacodynamic model, (2) a receptor association/dissociation model with a linear transduction function, and (3) a combined biophase distribution-receptor association/dissociation model with a linear transduction function. The results show that for fentanyl hysteresis is entirely determined by the biophase distribution kinetics, whereas for buprenorphine hysteresis is caused by a combination of biophase distribution kinetics and receptor association/dissociation kinetics. The half-time values of biophase equilibration (t(1/2, k(eo))) were 16.4 and 75.3 min for fentanyl and buprenorphine, respectively. In addition, for buprenorphine, the value of k(on) was 0.246 ml/ng/min and the value of k(off) was 0.0102 min(-1). The concentration-effect relationship of buprenorphine was characterized by a ceiling effect at higher concentrations (intrinsic activity alpha=0.56, 95% confidence interval (CI): 0.50-0.62), whereas fentanyl displayed full respiratory depressant effect (alpha=0.91, 95% CI: 0.19-1.62). |
Databáze: | OpenAIRE |
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