首页> 外文期刊>Journal of Liquid Chromatography & Related Technologies >QUANTITATIVE DETERMINATION OF MEMANTINE IN HUMAN PLASMA BY LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY: APPLICATION TO A BIOEQUIVALENCE STUDY
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QUANTITATIVE DETERMINATION OF MEMANTINE IN HUMAN PLASMA BY LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY: APPLICATION TO A BIOEQUIVALENCE STUDY

机译:液相色谱-串联质谱法定量测定人血浆中的美氮素:在生物等效性研究中的应用

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A simple, sensitive, and rapid liquid chromatography-tandem mass spectrometry method for determination of memantine in human plasma was established. A one-step protein precipitation with methanol was used to extract the analyte from plasma samples. Memantine and amantadine (internal standard, IS) were separated on a YMC-ODS-C18 column using 0.1% formic acid and methanol as a mobile phase at a flow rate of 0.3 mL/min. Detection was performed on positive ion mode of the transitions at 180.3→107.3 for memantine and 152.2→135.3 for IS by selected reaction monitoring (SRM). The assay was validated over the concentration range of 0.5-50 ng/mL with a lower limit of quantification (LLOQ) of 0.5 ng/mL. The intra- and inter-batch precision (RSD) were no more than 5.96% and 6.37%, respectively. The accuracy was from −3.02% to 7.74%. The validated method was successfully applied to a randomized, 2-period cross-over bioequivalence study in 22 healthy Chinese volunteers following a single oral dose of 10 mg memantine hydrochloride tablet. The simple, inexpensive protein precipitation and high-throughput method makes it a suitable and valuable tool in the investigation of the clinical pharmacokinetics and bioequivalence.View full textDownload full textKeywordsamantadine quantitation, bioequivalence, lC-MS/MS, memantine, pharmacokineticsRelated var addthis_config = { ui_cobrand: "Taylor & Francis Online", services_compact: "citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,more", pubid: "ra-4dff56cd6bb1830b" }; Add to shortlist Link Permalink http://dx.doi.org/10.1080/10826076.2011.637276
机译:建立了一种简单,灵敏,快速的液相色谱-串联质谱测定人血浆中美金刚的方法。使用甲醇一步一步沉淀蛋白质可从血浆样品中提取分析物。美金刚和金刚烷胺(内标,IS)在YMC-ODS-C 18 色谱柱上分离,使用0.1%甲酸和甲醇作为流动相,流速为0.3 mL / min。通过选定的反应监测(SRM),对美金刚胺在180.3→107.3和IS在152.2→135.3的过渡离子模式进行了检测。该测定方法在0.5-50 ng / mL的浓度范围内经过验证,定量下限(LLOQ)为0.5 ng / mL。批内和批间精度(RSD)分别不超过5.96%和6.37%。准确度从3.03.02%到7.74%。验证的方法已成功应用于22口服单剂量10 mg美金刚盐酸盐的22位健康中国志愿者的随机,2-周期交叉生物等效性研究。简单,廉价的蛋白质沉淀和高通量方法使其成为研究临床药代动力学和生物等效性的合适且有价值的工具。查看全文下载全文关键词金刚烷胺定量,生物等效性,LC-MS / MS,美金刚,药代动力学相关的var addthis_config = { ui_cobrand:“ Taylor&Francis Online”,servicescompact:“ citeulike,netvibes,twitter,technorati,delicious,linkedin,facebook,stumbleupon,digg,google,更多”,发布:“ ra-4dff56cd6bb1830b”};添加到候选列表链接永久链接http://dx.doi.org/10.1080/10826076.2011.637276

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