Liu-cong, . Preparation of Amitriptyline Hydrochloride-Chitosan Microspheres[J]. Journal of South China Normal University (Natural Science Edition), 2008, 1(4): 81-86 .
Citation:
Liu-cong, . Preparation of Amitriptyline Hydrochloride-Chitosan Microspheres[J]. Journal of South China Normal University (Natural Science Edition), 2008, 1(4): 81-86 .
Liu-cong, . Preparation of Amitriptyline Hydrochloride-Chitosan Microspheres[J]. Journal of South China Normal University (Natural Science Edition), 2008, 1(4): 81-86 .
Citation:
Liu-cong, . Preparation of Amitriptyline Hydrochloride-Chitosan Microspheres[J]. Journal of South China Normal University (Natural Science Edition), 2008, 1(4): 81-86 .
By using Amitriptyline Hydrochloride as the model drug,amitriptyline hydrochloride-chitosan microspheres were prepared by emulsion cross-linking techniques with ethylene glycol diglycidyl ether (EGDE) as a cross-linking agent. The physicochemical properties and the drug-release performances of the microspheres were investigated. EGDE has epoxy groups and cross-linking reaction occurred with the groups of -NH2 on CS. The microspheres have the color of white, a spherical shape and an average diameter about 12.32m. The drug loaded efficiency is 26.25% and the content of the drug is 6.56%(/). With the increase of the concentration of CS , the releasing ratio of Amitriptyline Hydrochloride decreases. The result indicated that the microspheres have a satisfactory performance of slowly releasing the drug of Amitriptyline Hydrochloride.