The preparation and properties of crosslinking guar gum (GG) were studied by using ethanol as a solvent, epichlorohydrin as a crosslinking agent and sodium hydroxide as a catalyst. Some factors affecting the crosslinking degree of the crosslinked GG were investigated: reaction time, reaction temperature, amount of crosslinking agent, pH and solvent concentration. The sedimentation volume method was selected to determine the crosslinking degree of the crosslinked GG. The crosslinking degree was obviously influenced by the pH, reaction temperature and the crosslinking agent. The crosslinking improved alkali and acid resistance, retrogradation and viscosity stability of GG. The crosslinked GG has a significantly narrower melting transition as compared with GG. Polymer Journal ( It hydrates fairly rapidly in cold water, which gives highly viscous pseudoplastic solutions of generally greater low-shear viscosity. GG and its derivatives served as thickener, stabilizer, blister and flocculant are employed in the food, textile, pharmaceutical and paper industries due to their special properties. [1][2][3][4] Much effort has been devoted to the study of appropriate systems with special properties in order to avoid or minimize the side effects and to improve the efficacy of the therapy in the field of drug delivery in the last decades. Polysaccharides appear to be very attractive for their peculiar physico-chemical characteristics. 5 GG is hydrophilic and swells in cold water, forming viscous colloidal dispersions or sols. This gelling property retards the release of the drug from the dosage form, increasing the likelihood of degradation in the colon. GG was found to be a colon-specific drug carrier in the form of matrix and compression-coated tablets as well as microspheres. The drug is inevitably dissolved, at least partially, because of the high pH level in the stomach. The modification of GG with borax or glutaraldehyde results in a product that is degraded by the enzymatic mixture of galactomannanase and a-galactosidase, possessing a higher buffer-uptake capacity as compared with native GG. The polysaccharides are crosslinked to a sufficient extent that they remain insoluble in water. [6][7][8][9][10] GG can be modified by etherification, esterification, oxidation or graft. The derivatives of GG may compensate for the disadvantages of natural GG. For example, a carboxymethyl derivative may increase the hydrophilicity and solution clarity of the galactomannans and make it more soluble in an aqueous solution. The oxidized GG can be quickly