Hello everyone,
I wanted to know when we perform in vitro drug release experiments and fit them into various mathematical models:
1. How do we choose the best model based on the graph or the R-square value or something else?
2. the n value is supposed to be calculated only for the Korsmeyer-Peppas model or for all the models?
I am getting confused. Please help me understand.
Thanking you in advance.