Table 2.
Model | Equation |
---|---|
Dissolution efficiency | DE = (∫0 t y · dt/y 100 · t) × 100% |
First-order | %D = 100(1 − e −kt) |
Biexponential | %D = 100[1 − (Ae −αt + Be −βt)] |
Zero-order | %D = kt |
Weibull | %D = 100[1 − e −(t/TD)b] |
Legend: %D: dissolved percentage, b: shape parameter, TD: time interval necessary to release 63.2% of the drug, k, α and β: kinetics constants, t: dissolution time, A and B: initial drug concentrations that contribute for the two dissolution stages.