首页> 外文期刊>Journal of separation science. >Quantification of ropivacaine and its major metabolites in human urine samples utilizing microextraction in a packed syringe automated with liquid chromatography-tandem mass spectrometry (MEPS-LC-MS/MS)
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Quantification of ropivacaine and its major metabolites in human urine samples utilizing microextraction in a packed syringe automated with liquid chromatography-tandem mass spectrometry (MEPS-LC-MS/MS)

机译:在装有液相色谱-串联质谱(MEPS-LC-MS / MS)的自动化注射器中使用微量萃取对人尿样品中的罗哌卡因及其主要代谢产物进行定量

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The determination of ropivacaine and its major metabolites in urine was performed using microextraction in a packed syringe as an on-line sample preparation method with LC and MS/MS. The sampling sorbent utilized was polystyrene polymer. [H-2(7)]ropivacaine was used as the internal standard. The lower LOQ was 5.0 nmol/L. The calibration curves were obtained within the concentration range 5-2000 nmol/L in urine. The regression correlation coefficients for urine samples were >= 0.999 for all runs. The between-batch accuracy and precision values were determined from six replicates of quality control (QC) samples at three different concentrations in human urine. The mean accuracy values for the QC samples, reported as the percentage difference from the nominal value, were in the range of 99-115 %. The precisions, given as the RSDs, were in the range 1.9-11 %. The present method is miniaturized and fully automated and can be used for pharmacokinetic and pharmacodynamic studies.
机译:尿液中罗哌卡因及其主要代谢物的测定是使用带包装的注射器中的微萃取作为LC和MS / MS在线样品制备方法进行的。使用的采样吸附剂是聚苯乙烯聚合物。 [H-2(7)]罗哌卡因用作内标。最低LOQ为5.0 nmol / L。在尿液中5-2000 nmol / L的浓度范围内获得校准曲线。所有尿液样本的回归相关系数均> = 0.999。批间准确度和精密度值是从人尿中三种不同浓度的质量控制(QC)样品的六个重复样品中确定的。 QC样品的平均准确度值报告为与标称值的百分比差,范围为99-115%。以RSD给出的精度在1.9-11%范围内。本方法是小型化的并且是全自动的,可以用于药代动力学和药效学研究。

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