RP-HPLC法同时测定利肝隆颗粒中4种成分的含量  被引量:2

Simultaneous determination of four constituents content in Liganlong granules by RP-HPLC

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作  者:吴庆芝 王冬梅[1] 张维萍[1] 金秀杰 李晓倩[1] 赵怀清[1] 

机构地区:[1]沈阳药科大学药学院,辽宁沈阳110016

出  处:《沈阳药科大学学报》2014年第11期891-895,共5页Journal of Shenyang Pharmaceutical University

摘  要:目的建立RP-HPLC法同时测定利肝隆颗粒中芒柄花素、五味子醇甲、五味子甲素、五味子乙素4种成分的含量。方法采用Diamonsil C18色谱柱(200 mm×4.6 mm,5μm)进行分离;流动相:乙腈-甲醇(体积比为85∶15)(A)-体积分数为0.1%的磷酸水溶液(B),梯度洗脱,流速:1.0 m L·min^-1,检测波长:254 nm,柱温:30℃。结果芒柄花素、五味子醇甲、五味子甲素、五味子乙素质量浓度分别在0.060 5~0.483 8 mg·L^-1(r=0.999 5,n=5)、3.390~27.12 mg·L^-1(r=0.999 7,n=5)、0.459 8~3.678 mg·L^-1(r=0.999 7,n=5)、1.818~14.54 mg·L^-1(r=0.999 6,n=5)内与峰面积呈良好的线性关系,方法的平均回收率分别为100.2%(RSD=1.1%,n=9)、99.1%(RSD=1.4%,n=9)、100.1%(RSD=1.4%,n=9)和99.4%(RSD=1.4%,n=9)。结论该方法可用于利肝隆颗粒的质量控制。Objective To establish an RP-HPLC method for determination of formononetin,schizandrol A,γ-schizandrin and deoxyschizandrin in Liganlong granules( traditional Chinese medicines). Methods The HPLC separation was achieved on a Diamonsil C18( 200 mm × 4. 6 mm,5 μm) at 30℃. The mobile phase consisted of acetonitrile-methanol( 85: 15)- 0. 1% phosphoric acid solution with gradient elution at a flowrate of 1. 0 m L·min- 1. The UV detection wavelength was set at 254 nm. Results The linear ranges were0. 060 5- 0. 483 8 mg·L^- 1( r = 0. 999 5,n = 5),3. 390- 27. 12 mg·L^- 1( r = 0. 999 7,n = 5),0. 459 8-3. 678 mg·L^- 1( r = 0. 999 7,n = 5),1. 818- 14. 54 mg·L^- 1( r = 0. 999 6,n = 5) respectively. The average recoveries( n = 9) of formononetin,schizandrol A,γ-schizandrin and deoxyschizandrin were 100. 2%( RSD = 1. 1%,n = 9),99. 1%( RSD = 1. 4%,n = 9),100. 1%( RSD = 1. 4%,n = 9) and 99. 4%( RSD =1. 4%,n = 9),respectively. Conclusions The method is simple,accurate,repeatable and can be used for quality control of Liganlong granules.

关 键 词:利肝隆颗粒 芒柄花素 五味子醇甲 五味子甲素 五味子乙素 高效液相色谱法 含量测定 

分 类 号:R917[医药卫生—药物分析学]

 

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