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作 者:文治瑞[1] 杨卫灵 田红红[3] 谭高好 乙引[3] 伍庆[2]
机构地区:[1]黔南民族师范学院生命科学系,贵州黔南558000 [2]贵州师范大学分析测试中心,贵阳550001 [3]贵州师范大学生命科学学院,贵阳550001
出 处:《中国实验方剂学杂志》2015年第7期39-42,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技支撑计划项目(2011BAI13B04-01);2012年度教育部"创新团队发展计划"项目(IRT1227)
摘 要:目的:应用气相色谱-质谱(GC—MS)联用法对淫羊藿挥发油进行指纹图谱研究。方法:采用水蒸气蒸馏法提取巫山淫羊藿和粗毛淫羊藿中的挥发油,利用GC—MS对其化学成分进行分析,通过GC—FID建立了淫羊藿挥发油指纹图谱的分析方法。气相色谱条件为HP—INNOWAX色谱柱,进样口温度260℃,分流比5:1;程序升温(初始温度60℃,保持10min,以2℃·min^-1升至250℃,保持13min)。GC—MS参数为柱流速1.0mL·min^-1,MS电子能量70eV,离子源温度230℃,四级杆温度180℃,传输线温度280℃,全离子扫描,扫描质量范围m/z40~550,溶剂延迟3min。GC—FID参数:柱流速1.5mL·min^-1,FID检测器温度260℃,氢气流量30mL·min^-1,空气流量300mL·min^-1,尾吹氮气30mL·min^-1。结果:获得了20份不同产地淫羊藿的指纹图谱峰。结论:该方法的精密度、稳定性和重复性均良好。为淫羊藿药材的质量控制提供了有效手段。Objective: To investigate the chromatographic fingerprints of volatile oil from Epimedii Folium by GC-MS. Method: The volatile oil was extracted from Epimedii Folium by steam distillation method, chromatographic fingerprints of which was detected and calculated by GC-FID, and the mutual fingerprints of ten kinds essential oil from Epimedii Folium was established. GC conditions: HP-INNOWAX column inlet temperature 260 ℃, the split ratio of 5:1 ; temperature program: initial temperature of 60 ℃ , keep 10 min, with 2 ℃·min^-1 rose to 250 ℃ , 13 min to maintain. GC-MS parameters: column flow rate 1.0 mL·min^-1, MS electron energy 70 eV, ion source temperature of 230 ℃ , the quadrupole temperature 180 ℃ , the transmission line temperature 280 ℃ , full-ion scan mass range m/z 40-550, solvent delay 3 min. GC-FID parameters: column flow rate 1.5 mL ·min^-1, FID detector temperature 260 ℃ , the hydrogen flow rate 30 mL·min^-1 , the air flow 300 mL ·min^-1, tail blowing nitrogen 30 mL ·min^-1 Result: The method was proved to be accuracy, reproducible and stability, by which the ideal fingerprints of volatile oil from Epimedii Folium were obtained. Conclusion: The methods set up are beneficial for the quality control of Epimedii Folium.
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