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首页> 外文期刊>Analytical and bioanalytical chemistry >Trimethylsilyldiazomethane derivatization coupled with solid-phase extraction for the determination of alendronate in human plasma by LC-MS/MS
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Trimethylsilyldiazomethane derivatization coupled with solid-phase extraction for the determination of alendronate in human plasma by LC-MS/MS

机译:三甲基甲硅烷基重氮甲烷衍生化-固相萃取-LC-MS / MS法测定人血浆中的阿仑膦酸盐

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Alendronate is an important representative of bisphosphonates, strongly polar compounds that lack chromophores. With rare exceptions, derivatization of the analytes is necessary for bioanalysis. In this study, a rapid liquid chromatography-tandem mass spectrometry method employing pre-column derivatization was developed and validated for the determination of alendronate concentrations in human plasma. The procedure was based on derivatization with trimethylsilyldiazomethane during solid-phase extraction on a weak anion-exchange solid-phase cartridge, which integrated sample purification and derivatization into one step. The alendronate derivative was eluted with methanol. Chromatographic separation was performed on a Capcell PAK-C18 column. The total run time was 6.5 min. The calibration curve was linear in the range 1.00-1,000 ng/mL using d6-alendronate as the internal standard. The lower limit of quantification was 1.00 ng/mL. The intra- and inter-assay precision (in RSD) calculated from quality control samples was less than 15%, and the accuracy was between 98.1% and 100.2%. The validated method was successfully applied to characterize the pharmacokinetic profiles of alendronate following the intravenous infusion of 5 or 10 mg alendronate sodium to healthy volunteers. [Figure not available: see fulltext.]
机译:阿仑膦酸酯是双膦酸酯的重要代表,双膦酸酯是缺乏生色团的强极性化合物。除极少数例外,分析物的衍生化是生物分析所必需的。在这项研究中,开发了一种采用柱前衍生化的快速液相色谱-串联质谱方法,并验证了其在人血浆中阿仑膦酸盐浓度的测定。该程序基于在弱阴离子交换固相小柱上固相萃取过程中用三甲基甲硅烷基重氮甲烷衍生化的过程,该过程将样品纯化和衍生化整合为一个步骤。阿仑膦酸酯衍生物用甲醇洗脱。在Capcell PAK-C18柱上进行色谱分离。总运行时间为6.5分钟。使用d6-阿仑膦酸盐作为内标,校准曲线在1.00-1,000 ng / mL范围内呈线性。定量下限为1.00 ng / mL。根据质量控制样品计算出的批内和批间精密度(相对标准偏差)小于15%,准确度在98.1%至100.2%之间。经验证的方法已成功应用于表征向健康志愿者静脉输注5或10 mg阿仑膦酸钠后阿仑膦酸钠的药代动力学特征。 [图不可用:请参见全文。]

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