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A novel fully validated LC-MS/MS method for quantification of pyridoxal-5\u27-phosphate concentrations in samples of human whole blood

机译:一种经过完全验证的新颖LC-MS / MS方法,用于定量人全血样品中的吡ido醛5 \ u27-磷酸盐浓度

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摘要

Quantification of pyridoxal-5′-phosphate (PLP) in biological samples is challenging due to the presence of endogenous PLP in matrices used for preparation of calibrators and quality control samples (QCs). Hence, we have developed an LC–MS/MS method for accurate and precise measurement of the concentrations of PLP in samples (20 μL) of human whole blood that addresses this issue by using a surrogate matrix and minimizing the matrix effect. We used a surrogate matrix comprising 2% bovine serum albumin (BSA) in phosphate buffer saline (PBS) for making calibrators, QCs and the concentrations were adjusted to include the endogenous PLP concentrations in the surrogate matrix according to the method of standard addition. PLP was separated from the other components of the sample matrix using protein precipitation with trichloroacetic acid 10% w/v. After centrifugation, supernatant were injected directly into the LC–MS/MS system. Calibration curves were linear and recovery was >92%. QCs were accurate, precise, stable for four freeze-thaw cycles, and following storage at room temperature for 17 h or at −80 °C for 3 months. There was no significant matrix effect using 9 different individual human blood samples. Our novel LC–MS/MS method has satisfied all of the criteria specified in the 2012 EMEA guideline on bioanalytical method validation.
机译:由于用于制备校准物和质量控制样品(QC)的基质中存在内源性PLP,因此对生物样品中的吡ido醛5'-磷酸(PLP)进行定量分析具有挑战性。因此,我们开发了一种LC-MS / MS方法,用于准确,精确地测量人全血样品(20μL)中的PLP浓度,该方法通过使用替代基质并最大程度地降低基质效应来解决此问题。我们使用包含在磷酸盐缓冲液(PBS)中的2%牛血清白蛋白(BSA)的替代基质来制作校正剂,QC,并根据标准添加方法将浓度调整为包括替代基质中的内源性PLP浓度。使用10%w / v的三氯乙酸进行蛋白质沉淀,将PLP与样品基质的其他成分分离。离心后,将上清液直接注入LC-MS / MS系统。校准曲线为线性,回收率> 92%。质量控制准确,精确,稳定,可进行四个冻融循环,并在室温下保存17小时或在-80°C下保存3个月。使用9种不同的人类血液样本没有明显的基质效应。我们新颖的LC-MS / MS方法满足了2012年EMEA关于生物分析方法验证的指南中指定的所有标准。

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