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采用气相色谱/负离子化学电离/质谱法对人血浆中的美金刚进行定量分析。

Quantitative analysis of memantine in human plasma by gas chromatography/negative ion chemical ionization/mass spectrometry.

作者信息

Leis Hans Jörg, Fauler Günter, Windischhofer Werner

机构信息

University Children's Hospital, Division of Analytical Biochemistry and Mass Spectrometry, Auenbruggerplatz 30, A-8036 Graz, Austria.

出版信息

J Mass Spectrom. 2002 May;37(5):477-80. doi: 10.1002/jms.303.

Abstract

A sensitive and specific method for the determination of memantine in human plasma is presented. Memantine was extracted from plasma and derivatized to the pentafluorobenzoyl derivative in a one-step procedure avoiding any sample concentration steps. Amantadine was used as an internal standard. The compounds were measured by gas chromatography/negative ion chemical ionization mass spectrometry without any further processing. Using this detection mode, the fragment ions at m/z 353 and 325 were obtained at high relative abundance. Calibration graphs were linear over the range 0.117-30 ng ml(-1). At the limit of quantification (LOQ), the inter-assay precision was 2.00% and the intra-assay variability was 3.22%. The accuracy at the LOQ showed deviations of -1.42% (intra-assay) and -2.47% (inter-assay). The method is rugged, rapid and robust and was applied to the batch determination of memantine during pharmacokinetic profiling of the drug.

摘要

本文介绍了一种灵敏且特异的测定人血浆中美金刚的方法。美金刚从血浆中提取出来,并在一步法中衍生化为五氟苯甲酰衍生物,避免了任何样品浓缩步骤。金刚烷胺用作内标。这些化合物不经任何进一步处理,通过气相色谱/负离子化学电离质谱法进行测定。采用这种检测模式,在高相对丰度下获得了质荷比为353和325的碎片离子。校准曲线在0.117 - 30 ng ml⁻¹范围内呈线性。在定量限(LOQ)处,批间精密度为2.00%,批内变异为3.22%。定量限处的准确度显示批内偏差为 -1.42%,批间偏差为 -2.47%。该方法耐用、快速且稳健,已应用于该药物药代动力学分析中美金刚的批量测定。

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