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Dissolution data were fitted to various kinetic models.
Weibull function fit well the dissolution data of MRICD.
In contrast to a previous report, the variability of the glibenclamide dissolution data was significantly lower.
The optimized conditions resulted in dissolution data that were close to the predicted values.
Good agreement was achieved between experimental dissolution data and the modeling results.
Lack of dissolution information (e.g., missing information on dissolution media volume, individual dissolution data, multimedia dissolution, etc).
At present, percolation thresholds in HPMC matrices have been estimated solely through the mathematical modelling of dissolution data.
The change in water composition along the column was monitored to provide both differential and integral dissolution data.
Both steady-state and transient dissolution data from dissolution experiments conducted at various effluent flow rates were used in the model calibration.
Figure 9 shows the Zn2+ dissolution data (displayed as percentage of the total nZnO concentration in each solution as a function of time).
The dissolution data were fitted into zero-order, first-order, Higuchi and Korsemeyer-Peppas models to identify the pharmacokinetics and mechanism of drug release.
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