HPLC法同时测定复方丹参滴丸中7个活性成分的含量  被引量:8

Simultaneous Determination of Seven Active Ingredients in Compound Danshen Dropping Pills by HPLC

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作  者:施法[1] 吴怡[2] 王洋[1] 

机构地区:[1]辽宁省食品药品检验所,沈阳110023 [2]辽宁省中医药研究院

出  处:《中国药师》2013年第3期339-341,共3页China Pharmacist

摘  要:目的:建立同时分析测定复方丹参滴丸中7种活性成分(丹参素钠、原儿茶醛、丹酚酸B、三七皂苷R_1、人参皂苷Rg_1、人参皂苷Re、人参皂苷Rb_1)的方法。方法:色谱柱为安捷伦Poroshell 120 SB-C_(18)(100mm×3.0 mm,2.7μm),以乙腈为流动相A,0.05%磷酸溶液为流动相B,梯度洗脱,流速:1.0 ml·min^(-1);检测波长分别为280,210 nm。结果:丹参素钠、原儿茶醛、丹酚酸B、三七皂苷R_1、人参皂苷Rg_1、人参皂苷Re、人参皂苷Rb_1的线性范围分别为0.020~0.408μg(r=0.999 9),0.020~0.401μg(r=0.999 8),0.021~0.415μg(r=0.999 9),0.004~0.080μg(r=0.999 9),0.004~0.080μg(r=0.999 9),0.004~0.080μg(r=0.999 9),0.004~0.080μg(r=0.999 8);平均加样回收率97.1%~102.4%,RSD<1.7%(n=9)。结论:该方法操作简单,重复性好,为评价和监控复方丹参滴丸的质量提供可靠的方法。Objective:To establish a method for the simultaneous determination of seven active ingredients(sodium salvianic A, protocatechualdehyde,salvianic acid B,notoginsenoside R_1,ginsenoside Rg,,ginsenoside Re and ginsenoside Rb_1 ) in compound Danshen dropping pills.Method:The determination was carried out with an Agilent Poroshell 120 SB-C_(18)(100 mm×3.0 mm, 2.7μm) column.The mobile phase consisted of acetonitrile(A)-0.05%phosphoric acid solution(B) with gradient elution at a flow rate of 1.0 ml·min^(-1).The detection wavelengths were 280 nm and 210 nm.Result:The calibration curves were linear within the range of 0.020-0.408μg for sodium salvianic A(r = 0.999 9 ),0.020-0.401μg for protocatechualdehyde(r = 0.999 8 ),0.021-0.415μg for salvianic acid B(r = 0.999 9),0.004-0.080μg for notoginsenoside R_1(r = 0.999 9),0.004-0.080μg for ginsenoside Rg_1(r = 0.999 9),0.004-0.080μg for ginsenoside Re(r= 0.9999) and 0.004-0.080μg for ginsenoside Rb_1(r = 0.999 8).The average recoveries were within the range of 97.1%-102-4%with RSD of less than 1.7%(n=9).Conclusion:The method is simple and repeatable,which can be applied in the quality control of compound Danshen dropping pills.

关 键 词:复方丹参滴丸 丹参素钠 原儿茶醛 丹酚酸B 三七皂苷R_1 人参皂苷Rg_1 人参皂苷RE 人参皂苷Rb_1 高效液相色谱法 

分 类 号:R927.2[医药卫生—药学]

 

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