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作 者:袁珂[1] 薛月芹[1] 殷明文[2] 楼炉焕[1]
机构地区:[1]浙江林学院天然药物研发中心,浙江临安311300 [2]郑州大学化学系,河南郑州450052
出 处:《中国中药杂志》2008年第19期2215-2218,共4页China Journal of Chinese Materia Medica
基 金:浙江省森林培育重中之重学科开放基金项目(200510)
摘 要:目的:建立RP-HPLC同时测定不同产地、不同采收期淡竹叶中荭草苷、异荭草苷、牡荆苷、异牡荆苷的含量。方法:采用高效液相色谱法,Waters XBridge C18色谱柱(4.6 mm×250 mm,5μm),以甲醇-0.05%冰醋酸(35∶65)为流动相洗脱,流速1.0 mL.min-1,检测波长340 nm,柱温25℃。结果:4种成分均达到基线分离,线性关系良好。方法的平均回收率及RSD分别为荭草苷103.2%,2.1%;异荭草苷101.6%,2.7%;牡荆苷98.4%,2.3%;异牡荆苷99.2%,1.8%。结论:本研究所建立的HPLC方法操作简便、结果准确可靠,为该类药材的入药及资源利用提供了依据。Objective: To develop a RP-HPLC method for simultaneous determination of orientin, isorientin, vitexin and isovitexin in Lophatherum gracile from different habitat and harvesting time. Method: The HPLC method was applied and the chromatographic column was a Waters XBridge C18 column (4. 6 mm×250 mm, 5μm). The mobile phase consisted of methanol- 0.05% acetic acid (35: 65). The flow rate was 1.0 mL·min^-1 and the detection wavelength was set at 340 nm. The column temperature was set at 25℃. Result: Four components were isolated well, the linear relationships were excellent. The mean recoveries and RSD values of orientin, isorientin, vitexin and isovitexin were 103.2%, 2. 1% ; 101.6%, 2. 7% ; 98.4%, 2. 3% ; 99.2% , 1.8%, respectively. Conclusion: The HPLC method is simple, sensitive and reliable, and can be used for the quality control of the medicinal material.
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