首页> 外文期刊>Analytical Chemistry >DIRECT DETERMINATION OF PANTOPRAZOLE ENANTIOMERS IN HUMAN SERUM BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY USING A CELLULOSE-BASED CHIRAL STATIONARY PHASE AND COLUMN-SWITCHING SYSTEM AS A SAMPLE CLEANUP PROCEDURE
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DIRECT DETERMINATION OF PANTOPRAZOLE ENANTIOMERS IN HUMAN SERUM BY REVERSED-PHASE HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY USING A CELLULOSE-BASED CHIRAL STATIONARY PHASE AND COLUMN-SWITCHING SYSTEM AS A SAMPLE CLEANUP PROCEDURE

机译:基于纤维素的手性固定相和色谱柱切换系统作为反相色谱柱反相高效液相色谱法直接测定人血清中的潘托唑对​​映体

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摘要

A direct stereoselective reversed-phase HPLC method is described for the determination of the enantiomers of a proton pump inhibitor, pantoprazole (PAN), in human serum. The enantiomers were separated with high resolution on a cellulose-based chiral stationary phase (Chiralcel OJ-R) following on-line solid phase sample cleanup with a column-switching device. A mixture of acetonitrile and 50 mM sodium perchlorate was used as the mobile phase at a flow rate of 0.5 mL/min. Pantoprazole enantiomers were detected by monitoring the column effluent with UV light at a wavelength of 290 nm. The calibration curve for each enantiomer was linear from 0.1 to 5.0 mu g/ mt. Under these conditions, the determination of pantoprazole enantiomers in human serum can be achieved with satisfactory selectivity, sensitivity, precision, and accuracy. The described procedure is very simple and rapid since labor-intensive sample preparation is not required. The method was applied to the analyses of the serum samples obtained from a volunteer who received an 80-mg oral dose of racemic PAN. The samples showed the (+)/(-) isomer ratios ranging from 0.74 to 1.03 up to 6 h after dosing, indicating that there is only a small difference in the concentrations of (+)- and (-)-PAN.
机译:描述了一种直接立体选择性反相HPLC方法,用于测定人血清中质子泵抑制剂pan托拉唑(PAN)的对映异构体。用柱切换装置在线固相样品净化后,在纤维素基手性固定相(Chiralcel OJ-R)上高分辨率分离对映体。乙腈和50 mM高氯酸钠的混合物用作流动相,流速为0.5 mL / min。通过用波长为290 nm的紫外光监测柱流出物来检测托拉唑对映体。每种对映异构体的校准曲线在0.1至5.0μg / mt之间呈线性关系。在这些条件下,可以以令人满意的选择性,灵敏度,精密度和准确性来测定人血清中的top托拉唑对映体。所描述的过程非常简单和快速,因为不需要劳动密集的样品制备。该方法用于从接受80毫克口服消旋PAN剂量的志愿者那里获得的血清样品的分析。样品在给药后最多6小时显示(+)/(-)异构体比率为0.74至1.03,表明(+)-和(-)-PAN的浓度仅存在很小的差异。

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