Objective: To explore the possibility of repairi ng long segmental bone defects and preventing infection with cefazolin loaded bo ne matrix gelatin (C-BMG).Methods: C-BMG was made from putting cefazolin into BMG by va...Objective: To explore the possibility of repairi ng long segmental bone defects and preventing infection with cefazolin loaded bo ne matrix gelatin (C-BMG).Methods: C-BMG was made from putting cefazolin into BMG by vac uum absorption and lyophilization techniques. The sustaining period of effective drug concentration in vitro and in vivo was detected. The time of inhibiting ba cteria,and the drug concentration in local tissues (bone and muscle) and plasma after implantation of C-BMG were examined by high performance liquid chromatog raphy. Results: The effective inhibition time to staphylococcus aureus of C-BMG was 22 days in vitro; while 14 days in vivo. The cefazolin concentrat ion in local tissues was higher in early stage,and later it kept a stable and l ow drug release. C-BMG showed an excellent ability to repair segmental long bon e defects.Conclusions: C-BMG can gradually release cefazolin with effect ive drug concentration and has excellent ability to repair segmental bone defect s. It can be used to repair segmental long bone defects and prevent infection af ter operation.展开更多
基金ThisprojectwassupportedbyagrantfromtheMinistryofHealth (No .96 1 14 5 )
文摘Objective: To explore the possibility of repairi ng long segmental bone defects and preventing infection with cefazolin loaded bo ne matrix gelatin (C-BMG).Methods: C-BMG was made from putting cefazolin into BMG by vac uum absorption and lyophilization techniques. The sustaining period of effective drug concentration in vitro and in vivo was detected. The time of inhibiting ba cteria,and the drug concentration in local tissues (bone and muscle) and plasma after implantation of C-BMG were examined by high performance liquid chromatog raphy. Results: The effective inhibition time to staphylococcus aureus of C-BMG was 22 days in vitro; while 14 days in vivo. The cefazolin concentrat ion in local tissues was higher in early stage,and later it kept a stable and l ow drug release. C-BMG showed an excellent ability to repair segmental long bon e defects.Conclusions: C-BMG can gradually release cefazolin with effect ive drug concentration and has excellent ability to repair segmental bone defect s. It can be used to repair segmental long bone defects and prevent infection af ter operation.
