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高效液相色谱法测定三七片中三七皂苷R1和人参皂苷Rg1的含量 被引量:14

Determination of Notoginsenoside R1 and Ginsenoside Rg1 in Sanqi Tablets by RP-HPLC
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摘要 目的:用RP-HPLC法测定三七片中三七皂苷R1和人参皂苷Rg1的含量。方法:以ZORBAXEXTEND-C18分析柱(4.6mm×250mm,5μm);乙腈-水(24∶76)为流动相;检测波长203nm;流速1.2mL.min^-1;柱温30℃。结果:三七皂苷R1在0.153-0.918μg内与峰面积呈良好的线性关系(r=0.99805);人参皂苷Rg1在0.786-4.716μg内与峰面积呈良好的线性关系(r=0.99949);回收率三七皂苷R1为97.15%,RSD=0.93%,人参皂苷Rg1为98.25%,RSD=0.68%。结论:方法简便、快速、重现性好,可作为三七片质量控制的辅助检测选项。 Objective :Determine the notogiensenoside R1 and giensenoside Rgl in Sanqi Tablets by RP - HPLC. Methods : ZORBAX EXTEND - C18 column (4.6mm × 250mm,5μm) was used as a stationary phase , aeetonitrile - water ( 24:76 ) as a mobile phase , and detection wavelength at 203nm, 1. 2mL·min^-1 of flow rate and 30℃ column temperature. Results: The calibration curves were linear in the range of 0. 153 - 0.918μg for notoginsenoside R1 ( r = 0.99805) and 0.786 - 4. 716 μg for ginsenoside Rgl ( r = 0.99949 ) . The Recovery of notoginsenoside R1 was 97.15% with RSD 0.93% , and that of ginsenoside Rgl was 98.25% with RSD 0.68%. Conclusion: The method is simple and quick with good reproducibility . It can be used as adjuvant determination for the quality control of Sanqi Tablets.
出处 《中华中医药学刊》 CAS 2008年第2期421-422,共2页 Chinese Archives of Traditional Chinese Medicine
关键词 三七片 三七皂苷R1 人参皂苷RG1 RP-HPLC 含量测定 Sanqi tablets notogiusenoside R1 ginsenoside Rg1 RP- HPLC determination
作者简介 俞坚(1970-),女,浙江杭州人,主管中药师,学士,研究方向:医院药学、中药鉴别。
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