建立了高效液相色谱测定罗汉果中罗汉果苷Ⅴ、罗汉果苷ⅣA、罗汉果苷Ⅲ、11-氧化罗汉果苷Ⅲ、罗汉果苷ⅡE和11-氧化罗汉果苷ⅡE等6种苷类化合物含量的方法.采用的色谱条件:ZORBAX SB-C18色谱柱(150 mm×4.6 mm, 5 μm);柱温30 ℃;以水(A相)和乙腈(B相)为流动相,梯度洗脱程序:0~3 min,20%B~30%B;3~8 min,30%B~35%B;8~9 min,35%B;流速0.8 mL/min;检测波长203 nm;进样量10 μL.结果表明,以上6种苷类化合物分别在0.04~1.0 mg/mL、0.011~0.68 mg/mL、0.010~0.80 mg/mL、0.0097~0.58 mg/mL、0.025~1.0 mg/mL、0.013~0.76 mg/mL范围内线性关系良好(r>0.9991).加标回收率依次为99.65% ,101.6% ,97.05% ,103.1% ,99.25% 和103.0% ;相对标准偏差分别为0.83% ,3.1% ,1.9% ,3.3% ,0.59% 和2.0% .该方法简便、快速、准确,适用于罗汉果原材料及其制品中苷类化合物的检测和含量测定.
参考文献
[1] | New Medical College of Jiangsu.Great Dictionary of chinese medicine.Shanghai:Shanghai Scientific & Technical Publishers (江苏新医学院.中药大辞典.上海:上海科学技术出版社),1977:1356 |
[2] | Takemoto T,Arihara S,Nakajima T,et al.Yakugaku Zasshi,1983,103(11):1151 |
[3] | Chang Q,Si J Y,Chen D H,et al.China Journal of Chinese Materia Medica (常琪,斯建勇,陈迪华,等.中国中药杂志),1995,20(9):554 |
[4] | Ukiya M,Akihisa T,Tokuda H,et al.J Agric Food Chem,2002,50:6710 |
[5] | Takasaki M,Konoshima T,Murata Y,et al.Cancer Lett,2003,198:37 |
[6] | Takeo E,Yoshida S,Tada S,et al.Atheroscler Thromb,2002,9:114 |
[7] | Li D P,Chen Y Y,Pan Z H,et al.Guihaia (李典鹏,陈月圆,潘争红,等.广西植物),2004,24(6):546 |
[8] | Li D,Ikeda T,Huang Y,et al.J Nat Med,2007,61:307 |
[9] | Pan Z H,Li D P,Chen Y Y,et al.Chinese Traditional and Herbal Drugs (潘争红,李典鹏,陈月圆,等.中草药),2004(Suppl):175 |
[10] | Li D P,Huang Y L,Liu J L,et al.Natural Product Research and Development (李典鹏,黄永林,刘金磊,等.天然产物研究与开发),2006,18(5):850 |
[11] | Li D P,Ikeda T,Matsuoka N,et al.Chem Pharm Bull,2006,54(10):1425 |
[12] | Li D P,Ikeda T,Nohara T,et al.Chem Pharm Bull,2007,55(7):1082 |
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