Tailoring or modulation of drug release from delivery systems comprises
a major area of research in pharmaceutical field where the primary
objective is to either sustain drug release or to design orodispersible
tablets. This objective can be successfully achieved by use of a class
of natural excipients - gums and mucilages. These polysaccharidic
plant-derived biopolymers because of their unique swellability in
aqueous medium can exert a retardant effect on drug release or can act
as superdisintegrant, depending on the concentration used in the
formulation. Mechanism of drug release from hydrophilic matrices
consisting of gums and mucilages is based on solvent penetration-induced
polymer relaxation, diffusion of entrapped drug followed by degradation
or erosion of the matrix. The degree and time-scale of swelling
contributes significantly to the kinetics of drug release. Drug
diffusion from polysaccharidic hydrogel may be of either Fickian, Case
II or anomalous transport type. The book has been designed to highlight
on the bifunctional aspect of the natural gums primarily because of
their concentration-dependent effect on drug release and their high
degree of swellability.