首页> 外文期刊>Analytical chemistry >Measurement of Deuterium-Labeled Phylloquinone in Plasma by High-Performance Liquid Chromatography/Mass Spectrometry
【24h】

Measurement of Deuterium-Labeled Phylloquinone in Plasma by High-Performance Liquid Chromatography/Mass Spectrometry

机译:高效液相色谱/质谱法测定血浆中氘标记的苯醌

获取原文
获取原文并翻译 | 示例
       

摘要

Phylloquinone (vitamin K_(1)) is a lipophilic compound present in plasma at low concentrations, which presents technical challenges for determining its bioavailability or metabolic fate using stable isotopes. We developed a method to simultaneously measure unlabeled and deuterium-labeled phylloquinone concentrations in plasma specimens using high-performance liquid chromatography/mass spectrometry with atmospheric pressure chemical ionization (LC-APCI/MS). Phylloquinone was extracted from plasma using hexane, further purified by solid-phase extraction, and then quantified using high-performance liquid chromatography with an APCI/MS as a detector. Plotting the expected versus the measured amount of serial dilutions of either unlabeled or labeled phylloquinone gave correlation coefficients (R) of 0.999 for both compounds. The minimum detectable concentrations of unlabeled and labeled phylloquinone were 0.05 and 0.08 pmol/injection, respectively. Pooled plasma samples spiked with between 0.5 and 32 nmol phylloquinone/L gave average recoveries of 96.7percent with 5.4percent relative standard deviation (RSD) for unlabeled phylloquinone and 96.2percent with 6.6percent RSD for labeled phylloquinone. Plasma phylloquinone concentrations determined by LC-fluorescence and LC-APCI/MS methods from healthy subjects (n velence 17) were not statistically different (P velence 0.13). The LC-APCI/MS method is a sensitive technique for simultaneous determination of both unlabeled and labeled phylloquinone and can be applied to bioavailability studies.
机译:苯醌(维生素K_(1))是血浆中低浓度的亲脂性化合物,使用稳定的同位素确定其生物利用度或代谢命运面临技术挑战。我们开发了一种使用高效液相色谱/质谱联用大气压化学电离(LC-APCI / MS)同时测量血浆样品中未标记和氘标记的叶绿醌浓度的方法。使用己烷从血浆中提取苯醌,通过固相萃取进一步纯化,然后使用高效液相色谱法(以APCI / MS作为检测器)进行定量。绘制未标记或标记的叶绿醌系列稀释液的预期稀释液与测量值的连续稀释图,得出两种化合物的相关系数(R)为0.999。未标记和标记的叶绿醌的最低可检测浓度分别为每次注射0.05和0.08 pmol。加标0.5-32 nmol的叶醌/ L的合并血浆样品,未标记的叶醌的平均回收率为96.7%,相对标准偏差(RSD)为5.42,而经标记的叶醌的平均回收率为96.2%,相对标准偏差为6.6%。通过LC荧光法和LC-APCI / MS方法测定的健康受试者血浆中叶绿醌浓度(见第17页)没有统计学差异(见第0.13页)。 LC-APCI / MS方法是同时测定未标记和标记的叶醌的灵敏技术,可用于生物利用度研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号