检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:郭建平 孙其荣[1,2,3] 周全[1,2,3] 姚康德[1,2,3]
机构地区:[1]解放军二七二医院 [2]上海第二军医大学药学院 [3]天津大学材料系
出 处:《中国药学杂志》1998年第10期598-601,共4页Chinese Pharmaceutical Journal
摘 要:目的:研究葛根黄酮乙基纤维素(EC)聚乙二醇(PEG)载药系统的释药效果。方法:拟定载药系统组成及制备工艺,用紫外分光光度法对葛根黄酮的含量及溶出度进行测定。结果:乙基纤维素、聚乙二醇及葛根黄酮三者的用量,乙基纤维素、聚乙二醇载药系统粒径大小,制备温度等对葛根黄酮的释放均有影响。载药系统理想的比例为ECPEG葛根黄酮(5∶0.4∶1)。载药系统可在1h内突释(60.51±3.63)%,后按零级释放,在10h左右释放完全(95.07±3.12)%。结论:EC-PEG葛根黄酮(5∶0.OBJECTIVE: To study the radix puerariae drug carrier systems with ethycellulosepolyethylene glycol (ECPEG). METHODS: The isoflavone drug carrier systems and the art of manufacturing were designed. UV was used to determine the content and dissolution of the samples. RESULTS: The release of isoflavones from loaded beads was influenced by quanlity of EGPEG4000, size of loaded beads and temperature, etc. The optimum ratio of isoflavones, EC and PEG was 1∶5∶0.4, which displayed a dissolution behavior of a quick release followed by a constant slow release with zero order kinetics. Desirable profile of drug release was otained.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.229