首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Direct and simultaneous analysis of loxoprofen and its diastereometric alcohol metabolites in human serum by on-line column switching liquid. chromatography and its application to a pharmacokinetic study
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Direct and simultaneous analysis of loxoprofen and its diastereometric alcohol metabolites in human serum by on-line column switching liquid. chromatography and its application to a pharmacokinetic study

机译:在线色谱柱切换液可直接同时分析人血清中洛索洛芬及其非对映体酒精代谢产物。色谱及其在药代动力学研究中的应用

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摘要

A simple, rapid, and accurate column-switching liquid chromatography method was developed and validated for direct and simultaneous analysis of loxoprofen and its metabolites (trans- and cis-alcohol metabolites) in human serum. After direct serum injection into the system, deproteinization and trace enrichment occurred on a Shim-pack MAYI-ODS pretreatment column (10 mm x 4.6 mm i.d.) by an eluent consisting of 20 mM phosphate buffer (pH 6.9)/acetonitrile (95/5, v/v) and 0.1% formic acid. The drug trapped by the pretreatment column was introduced to the Shim-pack VP-ODS analytical column (150 mm x 4.6 mm i.d.) using acetonitrile/water (45/55, v/v) containing 0.1% formic acid when the 6-port valve status was switched. Ketoprofen was used as the internal standard. The analysis was monitored on a UV detector at 225 nm. The chromatograms showed good resolution, sensitivity, and no interference by human serum. Coefficients of variations (CV%) and recoveries for loxoprofen and its metabolites were below 15 and over 95%, respectively, in the concentration range of 0.1-20 mu g/ml. With UV detection, the limit of quantitation was 0.1 mu g/ml, and good linearity (r = 0.999) was observed for all the compounds with 50 mu l serum samples. The mean absolute recoveries of loxoprofen, trans- and cis-alcohol for human serum were 89.6 +/- 3.9. 93.5 +/- 3.2, and 93.7 +/- 4.3%, respectively. Stability studies showed that loxoprofen and its metabolites in human serum were stable during storage and the assay procedure. This analytical method showed excellent sensitivity with small sample volume (50 mu l), good precision, accuracy, and speed (total analytical time 18 min), without any loss in chromatographic efficiency. This method was successfully applied to the pharmacokinetic study of loxoprofen in human volunteers following a single oral administration of loxoprofen sodium (60 mg, anhydrate) tablet. (c) 2006 Elsevier B.V. All rights reserved.
机译:建立了一种简单,快速,准确的色谱柱切换液相色谱方法,并验证了该方法可直接和同时分析人血清中洛索洛芬及其代谢产物(反式和顺式醇代谢物)。将血清直接注入系统后,在Shim-pack MAYI-ODS预处理柱(10 mm x 4.6 mm内径)上通过由20 mM磷酸盐缓冲液(pH 6.9)/乙腈(95/5)组成的洗脱液进行脱蛋白和痕量富集。 ,v / v)和0.1%的甲酸。在6位进样口中,使用含有0.1%甲酸的乙腈/水(45/55,v / v)将被预处理柱捕集的药物引入Shim-pack VP-ODS分析柱(150 mm x 4.6 mm内径)阀门状态已切换。酮洛芬用作内标。在225nm的UV检测器上监测分析。色谱图显示良好的分离度,灵敏度,并且不受人血清干扰。洛索洛芬及其代谢物的变异系数(CV%)和回收率分别在0.1-20μg / ml的范围内分别低于15%和超过95%。通过紫外检测,定量限为0.1μg / ml,对于含50μl血清样品的所有化合物,均观察到良好的线性(r = 0.999)。人血清洛索洛芬,反式和顺式酒精的平均绝对回收率为89.6 +/- 3.9。分别为93.5 +/- 3.2和93.7 +/- 4.3%。稳定性研究表明,人血中洛索洛芬及其代谢产物在储存和测定过程中是稳定的。该分析方法显示出极好的灵敏度,样品量小(50μl),精密度,准确性和速度都很好(总分析时间为18分钟),而色谱效率没有任何损失。单次口服洛索洛芬钠(60 mg,无水)片剂后,该方法已成功应用于洛索洛芬在人类志愿者中的药代动力学研究。 (c)2006 Elsevier B.V.保留所有权利。

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