HPLC法测定生丹颗粒中补骨脂素及异补骨脂素的含量

目的建立生丹颗粒中补骨脂素、异补骨脂素的含量测定方法。方法采用高效液相色谱法,以AgilentZorbaxSB-C18（4.6mm×250mm,5μm）为色谱柱;流动相：甲醇-水（50∶50）;检测波长：246nm;流速：1.0ml/min;柱温：40℃;结果补骨酯素在1.135～45.400μg·ml^-1范围内,浓度与峰面积呈良好的线性关系（r=0.9998）;异补骨酯素在1.035～41.400μg·ml^-1范围内,浓度与峰面积呈良好的线性关系（r=0.9999）;样品补骨脂素的平均回收率98.0%,RSD为1.1%（n=6）;异补骨脂素的平均回收率97.8%,RSD为0.9%。结论此方法简便、快速,可作为生丹颗粒中补骨脂素、异补骨脂素的含量测定方法。

Determination of Psoralen and Isopsoralen in Shengdan Keli by HPLC

Aim To establish an HPLC method of determining psoralen and isopsoralen in Shengdan keli. Methods HPLC, Agilent Zorbax SB-C18 （4.6ram × 250mm,5 μm） was used as the chromatographic column, and methanol-water（50： 50） was used as the mobile phase. The detection wavelength was 246nm; the flow rate was 1.0ml/ min; and the column temperature was 40℃. Results The liner range of psoralen was 1. 135 -45. 400μ g·ml^-1 （ r = 0. 999 8）, and the liner range of isopsoralen was 1. 035 -41. 400p, g·ml^-1（ r =0.999 9）. The average recovery of psoralen was 98.0%, RSD = 1.1% （ n =6） ; The average recovery of isopsoralen was 97.8% , RSD =0.9% （ n = 6） . Conclusion The results showed that this method was reliable, accurate and could be used to separate and determine psoralen and the isopsoralen in Shengdan keli.