In terms of the release of active ingredients Kollidon CL as a
disintegrant was the best compared to EFA and NSD in the tablets,
whereas in terms of erosion tablet formulations with EFA and NSD
were better than that of KCL. No antioxidant release was observed for
up to 80 min of dissolution. This may be attributed to the low amount
of antioxidant in the tablet compared to the total amount of dissolution
media. According to Kim and Fasihi, [26], drug release and matrix erosion operate simultaneously and an increase in release rate at a later
time period was evident in the case of some formulations, which may
be attributed to the heterogeneous nature of the matrix. This might
also be the argument in response to late antioxidant release from fruit
tablets during dissolution since fruit tablets are a heterogeneous matrix.