Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, Ontario, Canada; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Clin Biochem. 2022 Mar;101:35-41. doi: 10.1016/j.clinbiochem.2021.12.004. Epub 2021 Dec 8.
Measurement of quantitative levels of phenylalanine and tyrosine in blood is an essential test for the diagnosis of and monitoring genetic disorders associated with phenylalanine metabolism, such as phenylketonuria (PKU), tyrosinemia, and defects of tetrahydrobiopterin synthesis and recycling. We developed a highly accurate and fast liquid chromatography with tandem mass spectrometry (LC-MS/MS) method for the quantification of phenylalanine and tyrosine on dried blood spot (DBS). We also designed a performance score system to evaluate various calibration methods in matrix matched material.
Phenylalanine/tyrosine-free whole blood was used to make accurate and stable DBS calibrators. Six calibrators cover the range of 0-1000 µmol/L. Underivatized phenylalanine and tyrosine were extracted and measured by LC-MS/MS. Precision, accuracy, limit of quantification, recovery and carryover were validated. External quality assurance materials were also used to evaluate performance of multi-point calibrations and single-point calibrations.
The run time was 4.5-minute. Accuracy analysis showed good agreement with reference materials. Precision, recovery, and the lower and upper limit of quantification met the criteria. When phenylalanine and tyrosine concentrations were less than 150 µmol/L, the 5-point calibration without the calibrator of 1000 µmol/L had the best performance. When the concentrations were > 250 µmol/L, the single-point calibration of 500 µmol/L had the best performance.
We developed a simple, fast and highly accurate method for the detection of phenylalanine and tyrosine on DBS, with chromatographic separation and underivatized analysis. Based on the calibration performance, a 6-point calibration method is satisfying for this test. An optional dynamic calibration method, which includes 6-point calibration, 5-point calibration and single-point calibration, can further increase test reliability.
定量检测血液中苯丙氨酸和酪氨酸的水平是诊断苯丙氨酸代谢相关遗传疾病(如苯丙酮尿症、酪氨酸血症以及四氢生物蝶呤合成和循环缺陷)的必要测试。我们开发了一种高度准确和快速的液相色谱串联质谱(LC-MS/MS)方法,用于定量分析干血斑(DBS)中的苯丙氨酸和酪氨酸。我们还设计了一个性能评分系统,用于评估基质匹配材料中各种校准方法。
使用不含苯丙氨酸/酪氨酸的全血制作准确且稳定的 DBS 校准品。6 个校准品覆盖 0-1000μmol/L 范围。未衍生化的苯丙氨酸和酪氨酸通过 LC-MS/MS 进行提取和测量。验证了精密度、准确度、定量下限、回收率和交叉污染。还使用外部质量保证材料评估了多点校准和单点校准的性能。
运行时间为 4.5 分钟。准确度分析与参考材料具有良好的一致性。精密度、回收率以及定量下限和上限均符合标准。当苯丙氨酸和酪氨酸浓度<150μmol/L 时,无 1000μmol/L 校准品的 5 点校准具有最佳性能。当浓度>250μmol/L 时,500μmol/L 的单点校准具有最佳性能。
我们开发了一种简单、快速且高度准确的 DBS 上苯丙氨酸和酪氨酸检测方法,采用色谱分离和未衍生化分析。基于校准性能,6 点校准方法对此测试令人满意。可选的动态校准方法,包括 6 点校准、5 点校准和单点校准,可进一步提高测试可靠性。