首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Determination of captopril in biological samples by high-performance liquid chromatography with ThioGlo 3 derivatization.
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Determination of captopril in biological samples by high-performance liquid chromatography with ThioGlo 3 derivatization.

机译:ThioGlo 3衍生化高效液相色谱法测定生物样品中的卡托普利。

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Captopril, a well-known angiotensin converting enzyme (ACE) inhibitor, is widely used for treatment of arterial hypertension. Recent studies suggest that it may also act as a scavenger of free radicals because of its thiol group. Therefore, the present study describes a rapid, sensitive and relatively simple method for the detection of captopril in biological tissues with reverse-phase HPLC. Captopril was first derivatized with ThioGlo 3 [3H-Naphto[2,1-b]pyran,9-acetoxy-2-(4-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-y l)phenyl-3-oxo-)]. It was then detected by fluorescence-HPLC using an Astec C(18) column as the stationary phase and a water:acetonitrile:acetic acid:phosphoric acid mixture (50:50; 1 mL/L acids) as the mobile phase (excitation wavelength, 365 nm; emission wavelength, 445 nm). The calibration curve for captopril was linear over a range of 10-2500 nM and the coefficient of variation acquired for the within- and between-run precision for captopril was 0.5 and 3.8%, respectively. The detection limit of captopril with this method was found to be 200 fmol/20 microL injection volume. Its relative recovery from biological samples was determined to the range from 93.3 to 105.3%. Based on these results, we believe that our method is advantageous for captopril determination.
机译:卡托普利是一种众所周知的血管紧张素转化酶(ACE)抑制剂,被广泛用于治疗高血压。最近的研究表明,由于其硫醇基团,它也可以作为自由基的清除剂。因此,本研究描述了一种快速,灵敏且相对简单的方法,用于通过反相HPLC检测生物组织中的卡托普利。卡托普利首先用ThioGlo 3 [3H-萘并[2,1-b]吡喃,9-乙酰氧基-2-(4-(2,5-二氢-2,5-二氧代-1H-吡咯-1-基)苯基-3-氧代-)]。然后使用Astec C(18)色谱柱作为固定相并通过水:乙腈:乙酸:磷酸混合物(50:50; 1 mL / L酸)作为流动相(激发波长)进行荧光-HPLC检测365纳米;发射波长445纳米)。卡托普利的校准曲线在10-2500 nM的范围内是线性的,卡托普利的运行内和运行间精密度的变异系数分别为0.5和3.8%。发现该方法的卡托普利的检出限为200 fmol / 20 microL进样量。从生物样品中回收的相对含量确定为93.3%至105.3%。基于这些结果,我们认为我们的方法对于卡托普利的测定是有利的。

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