Glitazone Pharmacokinetics
From Proteopedia
(Difference between revisions)
(New page: {| class="wikitable" border="1" width="40%" style="text-align:center" |- ! colspan="6" align="center"| Glitazone Pharmacokinetics Comparison at Equivalent Dosages <ref>doi: 10.1111/j....) |
|||
| Line 45: | Line 45: | ||
! Hepatic <br/>(CYP2C8) | ! Hepatic <br/>(CYP2C8) | ||
|} | |} | ||
| + | For References, See: [[Treatments:Glitazone Pharmacokinetics References|References]] | ||
Revision as of 08:46, 10 December 2010
| Glitazone Pharmacokinetics Comparison at Equivalent Dosages [1][2][3][4] | |||||
|---|---|---|---|---|---|
| Parameter | Pioglitazone (Actos) | Rosiglitazone (Avandia) | |||
| Tmax (hr) | 1.8 | 1 | |||
| Cmax (ng/ml) | 617 | 361 | |||
| Bioavailability (%) | 83 | 99 | |||
| Protein Binding (%) | 99 | 99 | |||
| T1/2 (hr) | 3-8 | 3-4 | |||
| AUC (ng/ml/hr) | 6244 | 2024 | |||
| IC50 (nM) | 360 | 10 | |||
| Equivalent Dosage (mg) | 30 | 4 | |||
| Metabolism | Hepatic (CYP2C8) | Hepatic (CYP2C8) | |||
For References, See: References
