Design, optimization, and in vitro evaluation of orally disintegrating tablets containing amlodipine besylate
- Vol.58(4), Oct-Dec
- Banagalore Association of Pharmaceutical Teachers of India (APTI) 2024
- 1205-1214p.
In this study, it was aimed to prepare orally disintegrating tablet formulations of amlodipine besylate by applying the experimental design. Materials and Methods:
A face-centered, central composite 32 full factorial design was applied to evaluate the effects of filler ratio (MAN: MCC; X1) and super disintegrant percentage (SSG; X2) on the critical tablet characteristics such as tensile strength (Y1), disintegration time (Y2) and dissolution rate (5th min) (Y3).