Table 1.
Control | Acute ritonavir | Steady-state Ritonavir |
|
---|---|---|---|
IV alfentanil | |||
Maximum miosis (mm) | 5.4 ± 0.5 | 4.8 ± 0.8 | |
Maximum miosis/dose (mm/mg) | 5.0 ± 0.7 | 13.8 ± 3.8 a | |
AUEC0-∞/dose (mm•hr/mg) | 8.4 ± 3.3 | 24.5 ± 17.3 a | |
AUEC0-∞/dose ratio (ritonavir/control) | 3.1 (1.6, 6.1) | ||
CLIV, miosis (mg•mm−1•hre−1•kg−1) | 2.3 ± 2.3 | 1.0 ± 0.9 a | |
Effect t1/2 (hr) | 0.9 ± 0.4 | 1.4 ± 0.8 a | |
Oral alfentanil | |||
Maximum miosis (mm) | 3.3 ± 0.7 | 2.7 ± 0.9 | 2.4± 1.0 |
Maximum miosis/dose (mm/mg) | 1.1 ± 0.2 | 8.9 ± 3.5 a | 8.0 ± 3.7 a |
AUEC0-∞/dose (mm•hr/mg) | 3.0 ± 1.4 | 62.3 ± 46.1 a | 28.2± 14.6 b |
AUE0-∞/dose ratio (ritonavir/control) | 18.0 (10.9, 25.4) | 7.3 (4.2, 12.8) | |
CL/F miosis/F (mg•mm−1•hr−1•kg−1) | 5.8 ± 3.6 | 0.34 ± 0.20 a | 0.65 ± 0.67 a |
Effect t1/2 (hr) | 1.8 ± 1.0 | 6.5 ± 4.1 a | 2.9 ± 1.4 a |
Subjects received 15 and 5 μg/kg IV ALF at the control and ritonavir sessions, respectively, and 43 and 4.3 μg/kg oral ALF at the control and ritonavir sessions, respectively. Maximum miosis and AUC are shown normalized to dose. All other variables are not dose adjusted. Results (n=11) are the arithmetic mean ± SD, except the AUC0-∞/dose ratio (ritonavir/control), which is the geometric mean (90% CI). b Subjects received 6.0 mg IV and 11.2 mg oral methadone HCl at all sessions. Results are the mean ± SD (n=11) except the AUC0-∞/dose ratio (ritonavir/control), which is the geometric mean (90% CI).
Significantly different from control (p<0.05)
Significantly different from acute ritonavir (p<0.05)