摘要
目的:建立高效液相色谱法测定香菊感冒颗粒(无糖型)中刺槐素的含量。方法:刺槐苷使用甲醇超声提取并用盐酸水解在、ODS(5μm,4.6×250mm)柱上,以甲醇-水-冰醋酸(350:150:2)为流动相进行分离,流速1.0ml/min,340nm波长检测。结果:方法准确、精密度高、重现性好,浓度在2.00-10.00μg/ml范围内线性关系良好,r=0.9998,平均加样加收率为99.9%,RSD=0.41%(n=6)。结论:方法简便、专属、重现性好,可作为香菊感冒颗粒质量控制的一种方法。
Objective: To establish a method for the determination of acacetin in Xiangjuganmao Keli (no sweet). Methods: Acacetin in powdered herb was extracted by ultrasonator with methanol and was hydrolyzed with hydrochloric acid. Separation was accomplished on an ODS reversed phase column(5 μm, 4. 6 × 250 mm) with a mobile phase of methanol-water-acetic acid( 350: 150: 2). The detective wavelength was at 340 nm. Results: The method was accurate, the results were stable and reproducible. The linear range of calibration cure was within the concetration of 2. 00 - 10. 00 μg/ml ( r = 0. 9998 ). The average extraction recovery was 99.9% (n =6), RSD =0. 41% (n =6). Conclusion: The method is simple, convenient, sensitive, and reproducible for quality control of Xiangjuganmao Keli( no sweet).
出处
《中药材》
CAS
CSCD
北大核心
2006年第11期1233-1235,共3页
Journal of Chinese Medicinal Materials
关键词
香菊感冒颗粒
刺槐素
含量测定
高效液相色谱
Xiangjuganmao Keli ( no sweet)
Acacetin
Specifications determination
HPLC