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作 者:梁瑾[1] 刘小花[1] 任远 梁建娣[1] 党子龙[1] 封德梅 封士兰[1]
机构地区:[1]兰州大学药学院,兰州730000 [2]甘肃省中药药理与毒理学重点实验室(培育基地),兰州730000 [3]甘肃省第二人民医院,兰州730000
出 处:《中国实验方剂学杂志》2012年第17期70-74,共5页Chinese Journal of Experimental Traditional Medical Formulae
基 金:中央高校基本科研业务费专项资金(Lzujbky-2011-137);甘肃省科技重大专项项目(1002FKDA048);甘肃省中药药理与毒理学重点实验室开放基金项目(ZDSYS-KJ-2012-007)
摘 要:目的:采用高效液相色谱法-二极管阵列检测器-蒸发光检测器(HPLC-DAD-ELSD)联用技术对黄芪药材进行指纹图谱研究。方法:采用Waters 2695-SpursilTMC18色谱柱(4.6 mm×250 mm,5μm),流动相乙腈-水梯度洗脱,流速1.0 mL.min-1,柱温25℃,进样量20μL,检测波长254 nm。蒸发光散射检测器的条件为:漂移管温度112.8℃,载气流速3.2 L.min-1。结果:10批药材HPLC-DAD指纹图谱找到14个共有峰,鉴别了毛蕊异黄酮和芒柄花素;HPLC-ELSD指纹图谱找到9个共有峰,鉴别了毛蕊异黄酮苷、黄芪甲苷、黄芪皂苷Ⅲ、黄芪皂苷Ⅱ。结论:方法准确可靠,为全面控制黄芪药材质量提供了一种方法。Objective: To research the chromatography fingerprint of Radix Astragali with hyphenated technique of HPLC-DAD-ELSD. Method: The chromatography conditions were defined as SpursilTM C18 column (4.6mm×250mm,5μm) ; mobile phase was A: ACN, B: H2O, gradient elution; flow speed was 1.0 mL ·min-1 ; temperature of column was set at 25 ℃; injection volume was 20 μL; detected wavelength was at 254 nm. The ELSD conditions were as follows : the temperature of drift tube was 112.8 ℃ , the gas speed was 3.2 L .min- 1Result: In the chromatography fingerprint with HPLC-DAD of Radix Astragali, 14 common peaks were demarcated, calycosin and formononetin were identified; in the chromatography fingerprint with HPLC-ELSD of Radix Astragali, 9 common peaks were demarcated, calycosin-7-O-β-D-glucoside, astragaloside IV, astragaloside III and astragaloside II were identified. Conclusion: The method was accurate and reliable and the study may contribute in controlling of Radix Astragali.
关 键 词:黄芪 中药指纹图谱 高效液相色谱法-二极管阵列检测器-蒸发光检测器
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