海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
7期
24-26
,共3页
毛柳珺%陈薇%廖曾珍%赵志英
毛柳珺%陳薇%廖曾珍%趙誌英
모류군%진미%료증진%조지영
黄芩苷%滴丸%正交设计%体外溶出度
黃芩苷%滴汍%正交設計%體外溶齣度
황금감%적환%정교설계%체외용출도
Baicalin%Dripping pill%Orthogonal design%Dissolution in vitro
目的:优化黄芩苷滴丸制备工艺,考察药物体外释放度。方法以聚乙二醇6000(PEG 6000)-共聚维酮(PVP S630)为基质制备黄芩苷滴丸,以圆整度和重量差异为评价指标,通过正交试验优化制备工艺。结果最佳处方和制备工艺条件为:黄芩苷、PEG 6000、PVP S630质量比为1∶9∶1,滴制时药料温度80~90℃,滴距6cm,滴速30滴/min,二甲基硅油为冷却剂,冷却温度为10~15℃。制备的滴丸在40min的平均溶出度为86.54%。结论优选的黄芩苷滴丸制备工艺合理可行,能增加药物的溶出度。
目的:優化黃芩苷滴汍製備工藝,攷察藥物體外釋放度。方法以聚乙二醇6000(PEG 6000)-共聚維酮(PVP S630)為基質製備黃芩苷滴汍,以圓整度和重量差異為評價指標,通過正交試驗優化製備工藝。結果最佳處方和製備工藝條件為:黃芩苷、PEG 6000、PVP S630質量比為1∶9∶1,滴製時藥料溫度80~90℃,滴距6cm,滴速30滴/min,二甲基硅油為冷卻劑,冷卻溫度為10~15℃。製備的滴汍在40min的平均溶齣度為86.54%。結論優選的黃芩苷滴汍製備工藝閤理可行,能增加藥物的溶齣度。
목적:우화황금감적환제비공예,고찰약물체외석방도。방법이취을이순6000(PEG 6000)-공취유동(PVP S630)위기질제비황금감적환,이원정도화중량차이위평개지표,통과정교시험우화제비공예。결과최가처방화제비공예조건위:황금감、PEG 6000、PVP S630질량비위1∶9∶1,적제시약료온도80~90℃,적거6cm,적속30적/min,이갑기규유위냉각제,냉각온도위10~15℃。제비적적환재40min적평균용출도위86.54%。결론우선적황금감적환제비공예합리가행,능증가약물적용출도。
OBJECTIVE To investigate optimal preparation technology of Baicalin Dropping Pills and study its dissolution in vitro.METHODS The baicalin dropping pills were prepared with PEG 6000 and PVP S630 as ma-trix.Orthogonal design was conducted to explore the influencing factors of baicalin dropping pills by evaluating the in -dexes of roundness and weight difference.RESULTS The optimal technology conditions were as follows:the ratio of baicalin,PEG 6000 and PVP S630 as 1∶9∶1,temperature of dropping drug liquid 80~90℃,dropping distance 6cm, dropping speed 30d· min -1 ,dimethy-silicone oil as cooling agent and the cooling temperature was 10~15℃.The average dissolution amount of Baicalin from Dropping Pills was 86.54%at 40 min.CONCLUSION The optimized process of Baicalin Dropping Pills is reasonable and feasible ,which has a good effect on increasing the drug dissolu-tion.