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作 者:陈道阳[1] 孙平川[2] 黄健玲[3] 邓亚利[3]
机构地区:[1]广东省人民政府机关门诊部,广州510030 [2]陕西省中医药研究院,西安710003 [3]华南农业大学制药工程系,广州510642
出 处:《中国药房》2012年第7期629-632,共4页China Pharmacy
摘 要:目的:构建甘木通药材的薄层色谱(TLC)、高效液相色谱(HPLC)、傅里叶红外光谱(FTIR)、气相色谱-质谱(GC-MS)多谱图体系,控制其质量。方法:采用HPLC法测定药材中的山柰素含量,色谱柱为WatersXbridgeC18(250mm×4.6mm,5μm),流动相为乙腈-0.4%冰乙酸水溶液(梯度洗脱),检测波长为326nm;TLC法中甘木通石油醚部位与乙酸乙酯部位的展开剂分别为石油醚-甲醇(9:1)和氯仿-甲醇(9:1);采用FTIR法对石油醚和乙酸乙酯部位的特征吸收峰进行标注;采用GC-MS联用法分析甘木通的挥发油成分。结果:不同产地甘木通药材在TLC、HPLC与IR图中有共性的特征峰用于定性;HPLC测定山柰素含量可用于定量;GC-MS法共鉴定出37个组分。结论:多谱图体系可综合鉴定甘木通药材并用于其质量控制。OBJECTIVE:To establish the TLC,HPLC,FTIR and GC-MS fingerprints of Clematis filamentosa for quality control of it.METHODS:HPLC method was used to determine the content of kaempferide.The determination was performed on Waters Xbridge C18(250 mm×4.6 mm,5 μm) column with mobile phase consisted of acetonitrile-0.4% acetic acid(gradient elution).The detection wavelength was set at 326 nm;Developer of ligroin-methanol(9:1) and chloroform-methanol(9:1)were used in ligroin extract and acetic ether extract respectively in TLC.Absorption peaks were labeled in petroleum ether and ethyl acetate by FTIR.The volatile oil components were analyzed by GC-MS.RESULTS:The common characteristic peaks in TLC,HPLC and IR fingerprints of C.filamentosa were used for qualitative analysis;the content of kaempferide was measured by HPLC;37 components were identified by GC-MS.CONCLUSION:Multiple chromatograms can be used for comprehensive identification and quality control of C.filamentosa.
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