摘要
目的:建立复方丹参片中三七皂苷R_1、人参皂苷Rg_1、人参皂苷Rb_1、人参皂苷Rd的含量测定方法。方法:采用HPLC-ELSD法,使用C_18色谱柱,以乙腈-水为流动相进行梯度洗脱,流速1.0mL·min^-1,柱温25℃,蒸发光散射检测器漂移管温度50℃,载气流速1.5L·min^-1。结果:目标峰分离良好,三七皂苷R1、人参皂苷Rg_1、人参皂苷Rb_1、人参皂苷Rd的线性范围分别为5.14~102.80μg·mL^-1、20.16~322.56μg·mL^-1、40.24~402.40μg·mL^-1、10.06~100.60μg·~mL-1,平均回收率分别为98.1%、96.7%、101.5%和98.1%。结论:该方法简便、准确、耐用性好,可用于复方丹参片中三七皂苷R_1、人参皂苷Rg_1、人参皂苷Rb1、人参皂苷Rd含量的测定。
Objective:To establish HPLC-ELSD method to determine the contents of notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1 and ginsenoside Rd in Fufang Danshen Tablets. Methods:C18 columns were used with gradient elution of acetonitrile-water as mobile phase by flow rate of 1.0mL·min-1. The column temperature was 25℃. The ELSD heater temperature was 50℃. Air flow rate was 1.5L·min-1. Results: The measured peaks were completely separated from the other components in the peak. The linear ranges of notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1 and ginsenoside Rd were 5.14~102.80μg·mL-1, 20.60~322.56μg·mL-1, 40.24~402.40μg·mL-1 and 10.06~100.60μg·mL-1 respectively. The average recoveries of notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1 and ginsenoside Rd were 98.1%, 96.7%, 101.5% and 98.1% respectively. Conclusion: The method is simple and accurate with good robustness. It can be used for the determination of notoginsenoside R1, ginsenoside Rg1, ginsenoside Rb1 and ginsenoside Rd in Fufang Danshen Tablets.
出处
《世界中医药》
CAS
2013年第2期201-204,共4页
World Chinese Medicine