海峡药学
海峽藥學
해협약학
STRAIT PHARMACEUTICAL JOURNAL
2014年
6期
56-59
,共4页
赵薇%罗艳%赵运生%杨利
趙薇%囉豔%趙運生%楊利
조미%라염%조운생%양리
复方益肝灵胶囊%质量标准%薄层色谱法%高效液相色谱法
複方益肝靈膠囊%質量標準%薄層色譜法%高效液相色譜法
복방익간령효낭%질량표준%박층색보법%고효액상색보법
Compound Yiganling Capsules%Quality standard%TLC%HPLC
目的:完善、提高复方益肝灵胶囊质量控制方法。方法采用TLC法鉴别水飞蓟素和五仁醇浸膏;采用HPLC法以甲醇-水(55︰45)、甲醇-水(60︰40)为流动相,在检测波长287nm、250nm处分别测定水飞蓟宾和五味子醇甲。结果薄层色谱斑点清晰,分离度好,专属性强;水飞蓟宾在0.0988~1.976μg(r=0.9999)线性关系良好,平均加样回收率98.54%,RSD为1.8%;五味子醇甲在0.0951~1.902μg(r=0.9999)线性关系良好,平均加样回收率98.95%,RSD为1.5%。结论本法简便、可靠、准确,可用于复方益肝灵胶囊的质量控制。
目的:完善、提高複方益肝靈膠囊質量控製方法。方法採用TLC法鑒彆水飛薊素和五仁醇浸膏;採用HPLC法以甲醇-水(55︰45)、甲醇-水(60︰40)為流動相,在檢測波長287nm、250nm處分彆測定水飛薊賓和五味子醇甲。結果薄層色譜斑點清晰,分離度好,專屬性彊;水飛薊賓在0.0988~1.976μg(r=0.9999)線性關繫良好,平均加樣迴收率98.54%,RSD為1.8%;五味子醇甲在0.0951~1.902μg(r=0.9999)線性關繫良好,平均加樣迴收率98.95%,RSD為1.5%。結論本法簡便、可靠、準確,可用于複方益肝靈膠囊的質量控製。
목적:완선、제고복방익간령효낭질량공제방법。방법채용TLC법감별수비계소화오인순침고;채용HPLC법이갑순-수(55︰45)、갑순-수(60︰40)위류동상,재검측파장287nm、250nm처분별측정수비계빈화오미자순갑。결과박층색보반점청석,분리도호,전속성강;수비계빈재0.0988~1.976μg(r=0.9999)선성관계량호,평균가양회수솔98.54%,RSD위1.8%;오미자순갑재0.0951~1.902μg(r=0.9999)선성관계량호,평균가양회수솔98.95%,RSD위1.5%。결론본법간편、가고、준학,가용우복방익간령효낭적질량공제。
OBJECTIVE To improve the quality standard for Compound Yiganling Capsules.METHODS Si-lymarin and Extractive material from Fructus Schisandrae Chinensis in Compound Yiganling Capsules were identified by TLC.The silybin and Schisandrol A were determined by HPLC with a mobile phase of methanol -water ( 55∶45 ) and methanol-water (60∶40) respectively.The detection wavelengths were set at 287nm and 250nm.RESULTS The quality identification by TLC was clear ,specific and well separated.The calibration curve of silybin was linear within the range of 0.0988~1.976μg ( r=0.9999 ) , the average recovery rate was 98.54%, RSD was 1.8%.The calibration curve of schisandrol A was linear within the range of 0.0988~1.976μg( r=0.9999 ) ,the average recov-ery rate was 98.95%,RSD was1.5%.CONCLUSION The method is simple,reliable,accurate and can be used for the quality control for Compound Yiganling Capsules.