安徽医药
安徽醫藥
안휘의약
ANHUI MEDICAL AND PHARMACEUTICAL JOURNAL
2015年
5期
868-870
,共3页
党参饮片%党参炔苷%高效液相色谱法
黨參飲片%黨參炔苷%高效液相色譜法
당삼음편%당삼결감%고효액상색보법
Codonopsis pieces%lobetyolin%HPLC
目的:建立党参饮片中党参炔苷的含量测定方法,为党参饮片质量标准的完善提供参考。方法党参炔苷的含量测定采用HPLC法,C18色谱柱,流动相为乙腈—水(28∶72),流速为1 mL·min-1,柱温为35℃,检测波长为267 nm;水分、总灰分和浸出物按《中国药典》2010版一部标准检测。结果测定10批党参饮片,党参炔苷含量为0.2315~1.0744 mg·g-1;浸出物为57.5%~69.6%。结论党参饮片中党参炔苷的含量与浸出物量之间没有明显的一致性,应建立具体的量化指标,完善质量评价标准。
目的:建立黨參飲片中黨參炔苷的含量測定方法,為黨參飲片質量標準的完善提供參攷。方法黨參炔苷的含量測定採用HPLC法,C18色譜柱,流動相為乙腈—水(28∶72),流速為1 mL·min-1,柱溫為35℃,檢測波長為267 nm;水分、總灰分和浸齣物按《中國藥典》2010版一部標準檢測。結果測定10批黨參飲片,黨參炔苷含量為0.2315~1.0744 mg·g-1;浸齣物為57.5%~69.6%。結論黨參飲片中黨參炔苷的含量與浸齣物量之間沒有明顯的一緻性,應建立具體的量化指標,完善質量評價標準。
목적:건립당삼음편중당삼결감적함량측정방법,위당삼음편질량표준적완선제공삼고。방법당삼결감적함량측정채용HPLC법,C18색보주,류동상위을정—수(28∶72),류속위1 mL·min-1,주온위35℃,검측파장위267 nm;수분、총회분화침출물안《중국약전》2010판일부표준검측。결과측정10비당삼음편,당삼결감함량위0.2315~1.0744 mg·g-1;침출물위57.5%~69.6%。결론당삼음편중당삼결감적함량여침출물량지간몰유명현적일치성,응건립구체적양화지표,완선질량평개표준。
Objective To establish a method for the determination of lobetyolin in Codonopsis pieces,and provide reference values for improving quality standards of Codonopsis pieces.Methods Lobetyolin content was determined by HPLC(high pressure liquid chro-matography)method (column conditions:C18 column,mobile phase acetonitrile—water (28∶72),flow rate 1mL·min-1,column tem-perature 35 ℃,detection wavelength 267 nm.The moisture,total ash and extract were detected according to a standard in"The Chinese Pharmacopoeia of 2010 version".Results 10 batches of Codonopsis pieces were tested,and it was found that lobetyolin was 0.231 5 ~1.074 4 mg·g-1 and extract was 57.5%~69.6%.Conclusions There is no obvious consistency between the lobetyo-lin content and the extract amount,It is necessary to establish specific quantitative indicators to improve the criteria of quality eval-uation.