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作 者:张敏[1] 袁金斌[2] 黄加龙[1] 黄兴发[2] 王慧军[2]
机构地区:[1]现代中药制剂教育部重点实验室.江西中医学院,江西南昌330004 [2]江西中医学院,江西南昌330006
出 处:《时珍国医国药》2007年第1期109-111,共3页Lishizhen Medicine and Materia Medica Research
摘 要:目的以吴茱萸碱和吴茱萸次碱为对照品建立吴茱萸生物碱类的高效液相色谱法(HPLC)指纹图谱,为鉴定吴茱萸药材提供依据。方法色谱柱:Diarnonsil C18(250mm×4.6mm5μm)。流动相:乙腈-水梯度洗脱,梯度0-5min水80%。5-25min水80%-35%,25-55min水35%-0.5-60min水0。检测波长225nm,柱温25℃,进样量10μl。结果测定的20批吴茱萸样品有11个共有峰,共有峰相对保留时间的RSD为1.2%-2.5%。相对峰面积的RSD为2.3%-3.5%。结论该实验首次建立了中药吴茱萸中生物碱成分的HPLC指纹图谱,为不同产地和采收期的吴茱萸药材鉴别提供了科学依据。Objective Evodiamine and Rutaecarpine were used as reference substances to establish an HPLC fingerprint of alkaloid in Fructus Evodiae for identifying and evaluating its quality. Methods The alkaloid was separated on a Diamosil C18 column ( 250 mm × 4, 6 ram. 5 μm). The mobile phase consisted of acetonitrile and distilled water with gradient elution. The flow rate was 1.0 ml/min, The wavelength of UV detection was 225 nm, The column temperature was 25℃ and 10 μl was injected, Results There were 11 common peaks in the fingerprint of 20 samples. The RSD of the relative retention time of the common peaks was 1.2% - 2.5%, The RSD of the relative peak area was 2.3% - 3.5%. Conclusion The fingerprint of alkaloid in Fructus Evodiae was firstly established, and it was proved to be scientific and effective, It will be used to identify the quality and evaluate different origins and collection period of Fructus Evodiae.
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