中国药师
中國藥師
중국약사
CHINA PHARMACIST
2015年
2期
230-232
,共3页
陈黎%刘春霞%何秀丽%张秀华
陳黎%劉春霞%何秀麗%張秀華
진려%류춘하%하수려%장수화
白及%1 ,4-二 4-(葡萄糖氧)苄基 -2-异丁基苹果酸酯%原儿茶酸%咖啡酸%液相串联质谱法
白及%1 ,4-二 4-(葡萄糖氧)芐基 -2-異丁基蘋果痠酯%原兒茶痠%咖啡痠%液相串聯質譜法
백급%1 ,4-이 4-(포도당양)변기 -2-이정기평과산지%원인다산%가배산%액상천련질보법
Bletilla Striata%Militarine%Protocatechuic acid%Caffeic acid%LC-MS/MS
目的::采用Q-TRAP LC-MS/MS测定中药白及中活性成分militarine、原儿茶酸和咖啡酸的含量。方法:采用Supelco Discovery C-18(150 mm ×2.1 mm,3μm)色谱柱,以乙腈和水(含体积比0.1%甲酸)为流动相,梯度洗脱,流速为0.25 ml· min-1,AB Sciex 4000 Q-TRAP型质谱仪多重反应监测( MRM)扫描模式对白及对照药材和白及样品分别进行检测。结果:白及对照药材中militarine、原儿茶酸和咖啡酸的含量分别为1.1675,0.0626,0.0010 mg·g-1.白及供试品药材中militarine、原儿茶酸和咖啡酸的含量分别为0.7088,0.0011,0.0004 mg·g-1(n=3)。结论:该方法简便、准确、重现性好,可用于对中药白及中militarine、原儿茶酸和咖啡酸这三个成分进行定量分析。
目的::採用Q-TRAP LC-MS/MS測定中藥白及中活性成分militarine、原兒茶痠和咖啡痠的含量。方法:採用Supelco Discovery C-18(150 mm ×2.1 mm,3μm)色譜柱,以乙腈和水(含體積比0.1%甲痠)為流動相,梯度洗脫,流速為0.25 ml· min-1,AB Sciex 4000 Q-TRAP型質譜儀多重反應鑑測( MRM)掃描模式對白及對照藥材和白及樣品分彆進行檢測。結果:白及對照藥材中militarine、原兒茶痠和咖啡痠的含量分彆為1.1675,0.0626,0.0010 mg·g-1.白及供試品藥材中militarine、原兒茶痠和咖啡痠的含量分彆為0.7088,0.0011,0.0004 mg·g-1(n=3)。結論:該方法簡便、準確、重現性好,可用于對中藥白及中militarine、原兒茶痠和咖啡痠這三箇成分進行定量分析。
목적::채용Q-TRAP LC-MS/MS측정중약백급중활성성분militarine、원인다산화가배산적함량。방법:채용Supelco Discovery C-18(150 mm ×2.1 mm,3μm)색보주,이을정화수(함체적비0.1%갑산)위류동상,제도세탈,류속위0.25 ml· min-1,AB Sciex 4000 Q-TRAP형질보의다중반응감측( MRM)소묘모식대백급대조약재화백급양품분별진행검측。결과:백급대조약재중militarine、원인다산화가배산적함량분별위1.1675,0.0626,0.0010 mg·g-1.백급공시품약재중militarine、원인다산화가배산적함량분별위0.7088,0.0011,0.0004 mg·g-1(n=3)。결론:해방법간편、준학、중현성호,가용우대중약백급중militarine、원인다산화가배산저삼개성분진행정량분석。
Objective:To develop a Q-TRAP LC-MS/MS method for the content determination of militarine, protocatechuic acid and caffeic acid in Bletilla Striata. Methods:A Supelco Discovery C-18 (150 mm × 2. 1 mm, 3 μm) column was used and the mobile phase was acetonitrile-water containing 0. 1% formic acid (v/v) with gradient elution. The flow rate was 0. 25 ml·min-1. Bletilla Striata contrast medicinal materials and Bletilla Striata samples were detected by AB Sciex 4000 Q-MRM scan mode. Results: The content of militarine, protocatechuic acid and caffeic acid in the control herb of Bletilla Striata was 1. 167 5, 0. 062 6 mg·g-1 and 0. 001 0 mg·g-1 , respectively, and that in Bletilla Striata samples was 0. 708 8, 0. 001 1 mg·g-1 and 0. 000 4 mg·g-1 , respec-tively(n=3). Conclusion:The method is simple, accurate and reproducible. It can be used to quantitatively analyze militarine, pro-tocatechuic acid and caffeic acid in Bletilla Striata.