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出 处:《中国中药杂志》2011年第10期1327-1329,共3页China Journal of Chinese Materia Medica
摘 要:目的:建立HPLC同时测定决明子药材中蒽醌类和萘并吡喃酮类4种主要成分含量的方法,为决明子药材的质量控制提供依据。方法:采用Kromasil 100-5 C18色谱柱(4.6 mm×250 mm,5μm),流动相水-乙腈-四氢呋喃-冰醋酸(100∶23∶5∶1)等度洗脱。检测波长278 nm,柱温30℃,流速1.0 mL.min-1。结果:4种成分达到了基线分离。红链霉素龙胆二糖苷,决明子苷,aurantio-obtusin-6-O-β-D-glucopyranoside以及决明子苷B线性范围为0.2741.37,0.1530.765,0.3021.51,0.0520.26μg,相关系数r均为0.999 9。平均加样回收率分别为100.9%(RSD 1.8%),101.2%(RSD 1.2%),99.40%(RSD 2.2%),100.5%(RSD 1.6%)。结论:建立了高效液相测定决明子中4种主要成分含量的方法,该方法精确,简便,可靠,重现性好,可用于决明子药材的质量控制。Objective: To establish a HPLC method for the simultaneous determination of 4 major components in semen cassiae obtusifoline and provide valuable data for quality control of semen cassiae obtusifoline.Method: Kromasil 100-5 C18column(4.6 mm×250 mm,5 μm).Eluted with water: acetonitrile: tetramethylene oxide: glacial acetic acid(100∶23∶5∶1).Detecte at 278 nm.The flow rate was 1.0 mL·min-1.Result: Four compositions were separated well.Good linearies were obtained within the range of 0.274-1.37 μg,0.153-0.765 μg,0.302-1.51 μg and 0.052-0.26 μg for rubrofusarin gentiobioside,casside,aurantio-obtusin-6-O-β-D-glucopyranoside,casside B respectively.The average recoveries were 100.9%(RSD 1.8%),101.2%(RSD 1.2%),99.40%(RSD 2.2%),100.5%(RSD 1.6%).Conclusion: The method is accurate,reliable and convenient.It can be used to control the quality of semen cassiae obtusifoline and its products.
关 键 词:高效液相色谱法 决明子 红链霉素龙胆二糖苷 aurantio—obtusin-6-O-β-D—glucopyranoside 决明子苷 决明子苷 B 含量测定
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