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糖智宁胶囊定性定量方法研究 被引量:1

Qualitative and quantitative study of Tangzhining capsules
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摘要 目的建立糖智宁胶囊的定性定量方法。方法采用TLC法对糖智宁方中黄连进行定性鉴别,采用HPLC法测定糖智宁胶囊中葛根素和竹节参皂苷Ⅳa的含量。色谱柱为Kromasil C18柱(4.6 mm×250 mm,5μm);柱温30℃;以0.2%磷酸溶液-乙腈为流动相进行梯度洗脱;流速1 mL min-1;检测波长203 nm。结果薄层色谱鉴别中,特征斑点清晰、分离度好、专属性强、阴性样品无干扰;在HPLC法中,葛根素和竹节参皂苷Ⅳa线性范围分别是:0.122 4~1.836μg(r=0.999 9)、0.249 6~3.744μg(r=0.999 9);平均加样回收率分别为98.3%、97.1%;RSD分别为1.0%、0.7%。结论所建方法专属性强,重复性好,可用于糖智宁胶囊的质量控制。 Objective To establish a qualitative and quantitative research standard of Tangzhining capsules.Methods TLC was employed to identify Coptidis Rhizoma;puerarin and panax japonicas saponins Ⅳ a were determined by HPLC.The chromatograhic separation was Kromasil C18column(4.6 mm×50 mm,5 μm);and the column temperature was 30 ℃.A linear elution of 0.2% phosphoric acid aqueous solution-acetonitrile was adopted at the flow rate of 1 mL min-1.The UV detection wavelength was 203 nm.Results TLC spots were clear,well-separated and specific without interference of the negative control.Puerarin and panax japonicas saponins Ⅳ a had a good linearity at 0.1224-1.836 μg(r = 0.999 9) and 0.2496-3.744 μg(r = 0.999 9).The average recoveries were 98.3%(RSD = 1.0%) and 97.1%(RSD = 0.7%).Conclusion The established standard is suitable for the quality control of TZN capsules.
机构地区 陕西中医学院
出处 《中南药学》 CAS 2013年第3期235-237,共3页 Central South Pharmacy
基金 陕西省科技计划项目(编号:2011K16-04-04)
关键词 糖智宁胶囊 定性定量方法 葛根 珠子参 黄连 葛根素 竹节参皂苷Ⅳa 薄层色谱法 高效液相色谱法 Tangzhining capsule qualitative and quantitative research radix puerariae rhizome panacis majoris Coptis chinensis puerarin panax japonicas saponins Ⅳ a TLC HPLC
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