Glitazone Pharmacokinetics
From Proteopedia
(Difference between revisions)
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! Hepatic <br/>(CYP2C8) | ! Hepatic <br/>(CYP2C8) | ||
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| - | For References, See: [[Treatments:Glitazone Pharmacokinetics References|References]] | + | For Pharmacokinetic Data References, See: [[Treatments:Glitazone Pharmacokinetics References|References]] |
Current revision
| Glitazone Pharmacokinetics Comparison at Equivalent Dosages | |||||
|---|---|---|---|---|---|
| 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 Pharmacokinetic Data References, See: References
