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高效液相色谱法测定普肾片中卡托普利含量
引用本文:乔立业,陆崟,苏华,任海祥,王曙东.高效液相色谱法测定普肾片中卡托普利含量[J].中国药业,2013(2):20-21.
作者姓名:乔立业  陆崟  苏华  任海祥  王曙东
作者单位:中国人民解放军南京军区总医院制剂科
摘    要:目的建立测定普肾片中卡托普利含量的高效液相色谱法。方法采用C18色谱柱(250 mm×4.6 mm,5μm),0.01 mol/L磷酸二氢钠-甲醇-乙腈(75∶25∶5,磷酸调节pH至2.7~2.8)为流动相,流速为1.0 mL/min,检测波长为215 nm,柱温为40℃。结果卡托普利质量浓度在10.21~81.71μg/mL的范围内与峰面积呈良好线性关系,r=0.999 9,平均回收率为99.93%,RSD为1.25%(n=9)。结论该方法简便、准确,可作为该制剂的质量控制方法。

关 键 词:卡托普利  高效液相色谱法  含量测定

Determination of Captopril in Pushen Tablets by HPLC
Qiao Liye,Lu Yin,Su Hua,Ren Haixiang,Wang Shudong.Determination of Captopril in Pushen Tablets by HPLC[J].China Pharmaceuticals,2013(2):20-21.
Authors:Qiao Liye  Lu Yin  Su Hua  Ren Haixiang  Wang Shudong
Institution:(Department of Preparations,Nanjing General Hospital of Nanjing Military Region,Nanjing,Jiangsu,China 210002)
Abstract:Objective To establish a HPLC method for the determination of the captopril content in Pushen Tablets. Methods The C18 column(250 mm×4.6 mm,5 μm) was adopted with 0.01 mol/L sodium dihydrogen phosphate-methanol-acetonitrile (75:25:5, adjusting pH to 2.7-2.8 with phosphoric acid) as the mobile phase. The flow rate was 1.0 mL/min,the detection wavelength was 215 nm and the column temperature was at 40℃. Results The linear range of captopril was obtained between 10.21- 81.71μg/mL, r = 0. 999 9,the average recovery rate was 99. 93%, RSD 1.25% (n =9). Conclusion The established method is simple,accurate,and can be used for the quality control of this preparation.
Keywords:captopril  HPLC  content determination
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