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[摘要]
目的 建立同時(shí)測定蒼耳丸中連翹酯苷A和綠原酸的HPLC法。方法 采用HPLC法測定。色譜柱:Shim-pack VP-ODS(150 mm×4.6 mm,5 μm);流動(dòng)相:乙腈–0.2%磷酸溶液,梯度洗脫;體積流量:1.0 mL/min;檢測波長:330 nm;進(jìn)樣量:10 μL;柱溫:40 ℃。結(jié)果 連翹酯苷A在0.232~1.856 μg與峰面積積分值呈現(xiàn)良好的線性關(guān)系(r=0.999 6),平均回收率為97.82%,RSD值為1.55%;綠原酸在0.25~2.00 μg與峰面積積分值呈良好的線性關(guān)系(r=0.999 8),平均回收率為101.1%,RSD值為1.18%。結(jié)論 該方法簡便,結(jié)果準(zhǔn)確,重現(xiàn)性好,可作為蒼耳丸的質(zhì)量控制方法。
[Key word]
[Abstract]
Objective To establish a method for the simultaneous determination of forsythoside A and chlorogenic acid in Canger Pill. Methods HPLC method was adopted. A Shim-pack VP-ODS C18 colum (150 mm × 4.6 mm, 5 μm) was adopted with mobile phase consisted of acetonitrile - 0.2% phosphoric acid solution in gradient elution. Detection wavelength was set at 330 nm. The flow rate was 1.0 mL/min. The injection volume was 10 μL at column temperature 40 ℃. Results The linear ranges of forsythoside A and chlorogenic acid were 0.232 — 1.865 μg (r=0.999 6) and 0.25 — 2.00 μg (r=0.999 8), respectively. The average recoveries were 97.82% (RSD=1.55%) and 101.1% (RSD=1.18%), respectively. Conclusion The method is simple, practicable, and accurate, which could be used for the quality control of Canger Pill.
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