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对映体选择性高效液相色谱法测定人血浆中的奥美拉唑

Enantioselective high-performance liquid chromatographic determination of omeprazole in human plasma.

作者信息

Cairns A M, Chiou R H, Rogers J D, Demetriades J L

机构信息

Department of Drug Metabolism, Merck Research Laboratories, West Point, PA 19486, USA.

出版信息

J Chromatogr B Biomed Appl. 1995 Apr 21;666(2):323-8. doi: 10.1016/0378-4347(94)00587-u.

Abstract

A new stereoselective HPLC assay was developed to isolate omeprazole enantiomers from human plasma using C2 solid-phase extraction cartridges and an analogue was used as internal standard. Recoveries of the (+)-isomer were 83.4 and 89.7% at 100 and 250 ng/ml, respectively. Recoveries of the (-)-isomer were 78.4 and 82.8%, respectively. Recovery of the internal standard averaged 77.2%. Direct chiral separation of the enantiomers is achieved on a Resolvosil BSA-7 chiral column (15 cm x 4 mm I.D.) and a matching guard column. The mobile phase is a variable amount of n-propanol (0.05-1.0%) in 0.05 M ammonium phosphate buffer (pH 7.0) and the flow-rate is 1.5 ml/min. Drug absorbance is monitored at 302 nm. Standard curves are linear from 15 to 250 ng/ml for each enantiomer. The coefficients of variation for intra-day precision at each concentration over the range of the standard curve were between 0.98 and 10.87%. The coefficients of variation for inter-day precision for the analyses of omeprazole enantiomers in plasma (30 and 175 ng/ml) were less than 10% over a four month interval.

摘要

开发了一种新的立体选择性高效液相色谱法,使用C2固相萃取柱从人血浆中分离奥美拉唑对映体,并使用一种类似物作为内标。(+)-异构体在100和250 ng/ml时的回收率分别为83.4%和89.7%。(-)-异构体的回收率分别为78.4%和82.8%。内标的回收率平均为77.2%。对映体在Resolvosil BSA-7手性柱(15 cm×4 mm内径)和匹配的保护柱上实现直接手性分离。流动相是0.05 M磷酸铵缓冲液(pH 7.0)中不同量的正丙醇(0.05 - 1.0%),流速为1.5 ml/min。在302 nm处监测药物吸光度。每种对映体的标准曲线在15至250 ng/ml范围内呈线性。在标准曲线范围内,每个浓度的日内精密度变异系数在0.98%至10.87%之间。在四个月的时间间隔内,血浆中奥美拉唑对映体分析(30和175 ng/ml)的日间精密度变异系数小于10%。

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