Objective:In the medium of ethanol(non-polar),STMP and ADH as crosslinkers to HA,to prepare drug delivery microspheres by getting stable cross-linked products without a gel phase,and to study biocompatibility and biod...Objective:In the medium of ethanol(non-polar),STMP and ADH as crosslinkers to HA,to prepare drug delivery microspheres by getting stable cross-linked products without a gel phase,and to study biocompatibility and biodegradability of cross-linked products.Methods:ISO10993.1-Safety Evaluation of Biomedical materials as a reference,to make hemolysis test,percutaneous stimulation test,acute toxicity test,and analyze in vitro degradation test,and degradation products.Results:HA-STMP cross-linked product had no hemolysis,no irritation,no acute systemic toxicity,but HA-ADH had a mild skin irritation and adverse acute systemic toxicity.HA-STMP cross-linked product had lower sensitivity on HAse and the curve is flatting.With the increase of degradation time HA-STMP results were changed by the structure analysis,degradation products of these cells were no toxicity.Conclusion:HA-STMP cross-linked products with better biocompatibility and better resistance to hydrolysis could delay the degradation time,which is suitable for the preparation of biodegradable drug carriers.展开更多
文摘Objective:In the medium of ethanol(non-polar),STMP and ADH as crosslinkers to HA,to prepare drug delivery microspheres by getting stable cross-linked products without a gel phase,and to study biocompatibility and biodegradability of cross-linked products.Methods:ISO10993.1-Safety Evaluation of Biomedical materials as a reference,to make hemolysis test,percutaneous stimulation test,acute toxicity test,and analyze in vitro degradation test,and degradation products.Results:HA-STMP cross-linked product had no hemolysis,no irritation,no acute systemic toxicity,but HA-ADH had a mild skin irritation and adverse acute systemic toxicity.HA-STMP cross-linked product had lower sensitivity on HAse and the curve is flatting.With the increase of degradation time HA-STMP results were changed by the structure analysis,degradation products of these cells were no toxicity.Conclusion:HA-STMP cross-linked products with better biocompatibility and better resistance to hydrolysis could delay the degradation time,which is suitable for the preparation of biodegradable drug carriers.
