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作 者:张金红[1] 房德敏[1] 陈然[2] 高颖[1] 王巨存[1] 郑榕[1] 冯鑫[1] 赵薇[1] 虎冲[2]
机构地区:[1]天津市天津医院,天津300211 [2]天津医科大学临床医学院,天津300270
出 处:《中国药房》2014年第11期1037-1039,共3页China Pharmacy
摘 要:目的:建立消肿接骨贴中苷类成分的定性定量方法。方法:应用薄层色谱(TLC)法对制剂中的续断和黄芪同时进行定性鉴别,以三氯甲烷.甲醇.水(13:7:2,V/V/功的下层溶液为展开剂,10%(V/V)的硫酸乙醇溶液为显色剂。应用高效液相色谱(HPLC)法对制剂中的柚皮苷进行含量测定:色谱柱为ThermoC18(250mm×4.6mm,5μm),流动相为乙腈-水(18:82,刃功,检测波长为283nm。结果:续断和黄芪的TLC斑点清晰、分离良好,阴性对照无干扰。柚皮苷进样量在0.0621-0.6210μg范围内与其峰面积积分值呈良好线性关系(r=0.9997);精密度、稳定性、重复性试验的RSD〈2%;平均加样回收率为99.3l%,RSD=1.73%(n=9)。结论:本研究建立的方法专属性强、灵敏度高、简便、准确、重复性好,可以用于消肿接骨贴中苷类成分的定性定量研究。OBJECTIVE: To establish a method for qualitative and quantitative study of glycosides in Xiaozhong jiegu plaster. METHODS :Dipsacus asper and Astragali Radix were identified simultaneously by TLC using chloroform-methyl alcohol-water( 13: 7:2, V/V/V)as developing solvent and 10 % (V/V)sulfuric acid ethanol as chromogenic agent. HPLC method was used to determine the content of naringin. The determination was performed on Thermo C18(250 min×4.6 mm, 5 μm) with mobile phase consisted of acetonitrile-water(18 : 82, V/V) and the detection wavelength was set at 283 nm. RESULTS: TLC spots ofD. asper and Astragali Radix were clear and well-separated without interference from negative control. The linear range of naringin was 0.062 1-0.621 0 μg (r=0.999 7) with an average recovery of 99.31% (RSD= 1.73 %, n=9). RSD of precision, stability and reproducibility tests were all lower than 2%. CONCLUSIONS: The method is specific, sensitive, simple, accurate and reproducible, and it is suitable for qualitative and quantitative identification of glycosides in Xiaozhong jiegu plasters.
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