Sensitive high-performance liquid chromatographic method for determination of captopril in plasma

M Amini , A Zarghi , H Vatanpour
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引用次数: 50

Abstract

A rapid, simple and sensitive high-performance liquid chromatographic method for the determination of captopril in plasma has been developed. Captopril is derivatized with a new reagent, 2-bromo-2′-acetonaphthone to form a product that showed ultraviolet-absorbing properties. For plasma samples, the protein was removed with 6% perchloric acid and the derivatized captopril was extracted with diethyl ether. The chromatographic separation was performed on an analytical μbondapak NH2 column (300×3.9 mm, i.d) with an isocratic mobile phase consisting of n-hexane–2-propanol–methanol–acetic acid (68:15:15:2). Using ultraviolet detection at 246 nm, the quantification limit for captopril in plasma was 10 ng/ml. The calibration curve was linear over the concentration range 12.5–500 ng/ml. The average recovery was 95% for plasma. The inter-day and intra-day assay coefficients of variation were found to be less than 12%.

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高效液相色谱法测定血浆中卡托普利的含量
建立了一种快速、简便、灵敏的高效液相色谱法测定血浆中卡托普利的方法。卡托普利与一种新的试剂2-溴-2 ' -乙萘酮衍生,形成具有紫外线吸收性能的产物。血浆样品用6%的高氯酸除去蛋白质,用乙醚提取衍生的卡托普利。色谱柱为μbondapak NH2 (300×3.9 mm, id),流动相为正己烷- 2-丙醇-甲醇-乙酸(68:15:15:2)。采用246 nm紫外检测,血浆中卡托普利的定量限为10 ng/ml。在12.5 ~ 500 ng/ml浓度范围内,校准曲线呈线性。血浆的平均回收率为95%。日间和日间测定变异系数均小于12%。
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