Table 2.
Symbol | Meaning | Value (min–1) |
---|---|---|
K10 | Elimination rate constant from the periocular site | 0.072 |
K12 | Absorption rate constant for cornea | 2.11e-7 |
K20 | Elimination rate constant from the cornea | 0.065 |
The finalized model (Fig. 1E) for corneal pharmacokinetics of celecoxib after periocular administration in rats was used as the model, and curve fitting was performed to obtain the parameter estimates. Since the drug was administered as a solution, the drug dissolution/release step in the model was not included.