首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Evaluation of matrix effects using a spike recovery approach in a dilute-and-inject liquid chromatography-tandem mass spectrometry opioid monitoring assay
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Evaluation of matrix effects using a spike recovery approach in a dilute-and-inject liquid chromatography-tandem mass spectrometry opioid monitoring assay

机译:在稀释和注射液相色谱-串联质谱阿片样物质监测分析中使用加标回收方法评估基质效应

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Background: Liquid chromatography-tandem mass spectrometry has become the gold standard for quantitative analysis of compounds in human matrices. Introduction of these assays into clinical practice, where false positive and false negative results have substantial implications, requires careful attention to matrix effects. We describe an evaluation of matrix effects in human urine from a dilute-and-inject liquid chromatography-tandem mass spectrometric assay for the quantitative analysis of opioids and metabolites.Methods: A spike-recovery approach was employed for each analyte in each sample. We examined the impact of spike-recovery for the 6 glucuronides measured in this assay and compared the analytes for which conventional stable isotope-labeled internal standards were used with the analytes for which analog internal standards were used.Results: For analytes that had analog internal standards, up to 1.5% of negative samples failed our requirement of recovering at least 80% of the expected spiked concentration while passing all other quality control parameters. Conclusions: Using spike-recovery as a quality control parameter decreases the rate of false negatives for compounds using analog internal standards, but does not have benefit for compounds with conventional stable isotope-labeled internal standards.
机译:背景:液相色谱-串联质谱法已成为定量分析人体基质中化合物的金标准。将这些检测方法引入临床实践时,假阳性和假阴性结果会产生重大影响,因此需要特别注意基质效应。我们描述了一种稀释液-进样液相色谱-串联质谱法对人尿中基质作用的评估,以对阿片类药物和代谢物进行定量分析。方法:对每种样品中的每种分析物采用加标回收法。我们检查了此测定中测量的6种葡糖醛酸苷加标回收率的影响,并将使用常规稳定同位素标记内标的分析物与使用内标类似物的分析物进行了比较。结果:对于具有内标类似物的分析物标准中,多达1.5%的阴性样品未能通过我们要求通过所有其他质量控制参数的同时至少回收预期加标浓度的80%的要求。结论:使用加标回收率作为质量控制参数可降低使用模拟内标物的化合物的假阴性率,但对于使用常规稳定同位素标记的内标物的化合物则无益。

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