4.6. Evaluation of the Prepared Tablets Weight uniformity, hardness, friability, and disintegration time were all evaluated according to the USP 32 for the tablet dosage form. A dissolution test was performed using USP apparatus type II (Paddle Apparatus, Erweka® DT600 dissolution test system (...
To minimise the crossover effect of residual taste, participants were instructed to wait 10 min from completing the evaluation of one test sample and commencing on the next test sample. After tasting each sample, participants were asked to rate how much they liked the sample and their ...