“…The particles in contact with the fluid starts to dissolve. At the same time the fluid enters the tablet through the pores and its network resulting in the disintegration of the tablet into smaller pieces and this stage is effectively controlled by the concentration of pores [ 242 , 243 , 244 , 245 , 246 , 293 , 345 , 346 , 347 ]. By extracting the information of the pore network and its permeability from a SEM image, Zhang et al [ 348 ] has shown that one can estimate the drug release rate by computational fluid dynamic simulation.…”