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反相高效液相色谱法测定治偏痛胶囊中芍药苷的含量 被引量:2

Quantitative Determination of Paeoniflorin in Zhipiantong Capsules by High Performance Liquid Chromatography
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摘要 目的 建立治偏痛胶囊中芍药苷的含量测定方法。方法 采用高效液相色谱法。使用Ultrasphere ODS(250mm×4.6mm,5μm)分析柱,流动相为甲醇-水(35:65),流速为1ml/min,检测波长为230nm,柱温26℃。结果 芍药苷的线性范围为0.47-4.7mg,平均加样回收率为97.3%,RSD为1.23%。制剂中芍药苷的含量限度规定不得少于4mg/粒。结论 方法简便可行,快速准确,重现性好,可很好的应用于治偏痛胶囊中芍药苷的含量测定。 Objetive To establish a reversed-phase HPLC method for the quantitative determination of Paeoniflorin in Zhipiantong Capsules. Methods The experimental conditions were as follows: Uhasphere ODS column (250 mm×4.6 mm,5μm), mobile phase : methanol-water( 35 : 65 ), flow rate: 1 ml/min, detective wavelength : 230 nm, column temperatre: 26℃. Results The calibration curve of Paeoniflorin showed a good linearity within the range of 0.47- 4.7 mg. The regression equation was Y = 1 262 X-39.31 ,being with a correction coefficient of =0. 999 9. The sample was stable in methanol within 24 h. The average recovery was 97.3% and RSD was 1.23%. We propse that the content of Paeoninflorin in the capsules should be no less than 4 mg each. Conclusion The established method is simple, feasible, fast, accurate, reproducible and reliable to operate and suitable for the quality control of Zhipiantong Capsules.
出处 《时珍国医国药》 CAS CSCD 北大核心 2006年第4期574-575,共2页 Lishizhen Medicine and Materia Medica Research
关键词 治偏痛胶囊 芍药苷 高效液相色谱法 Zhipiantong Capsules Paeoniflofin HPLC
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