Department of Pharmacy, Peking University Third Hospital, Beijing, 100191, China.
Therapeutic Drug Monitoring and Clinical Toxicology Center of Peking University, Beijing, 100191, China.
Anal Bioanal Chem. 2020 May;412(12):2763-2775. doi: 10.1007/s00216-020-02436-8. Epub 2020 Mar 4.
Pheochromocytoma and paraganglioma (PPGL) are rare neuroendocrine tumors arising from adrenal and extra-adrenal chromaffin cells. They produce excessive amounts of catecholamines and their metabolites. A newly analytical procedure based on the semi-automated microextraction by packed sorbent (MEPS) technique, using a digitally controlled syringe (eVol) combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS), was developed to quantify free urinary catecholamines and metanephrines. The important parameters affecting MEPS performance, namely the type of sorbent material (porous graphitized carbon (PGC), polar enhanced polymer (PEP), cation-exchange (CX) and C18), number of extraction cycles, and elution solvent system, were evaluated. The optimal experimental conditions involved the loading of sample mixture in seven extraction cycles through a C18 sorbent in a MEPS syringe, followed by using elution solutions (water/acetonitrile/formic acid, 95/4.75/0.25). The entire sample preparation took about 4 min. Chromatographic separation was well achieved with an HSS PFP column using the gradient elution. The linearity range of the method was 0.167-33.4 ng/mL for epinephrine, 0.650-130 ng/mL for norepinephrine, 1.53-306 ng/mL for dopamine, 1.34-268 ng/mL for metanephrine, 3.43-686 ng/mL for normetanephrine, and 1.33-265 ng/mL for 3-methoxytyramine. The intra- and interassay precisions were ≤ 12.8%, and the respective accuracies were 88.4-112.0% and 89.0-109.5%. The carryover and sample stability without acidification were also investigated. Validation using clinical urine specimens showed that the proposed method had higher sensitivity compared with other urinary biochemical tests. The developed MEPS-LC-MS/MS method was simple, fast, and cost-effective; it helped to obtain information about multiple metabolites. It is applicable in routine clinical laboratories for the screening of PPGL. Graphical abstract.
嗜铬细胞瘤和副神经节瘤 (PPGL) 是一种罕见的神经内分泌肿瘤,起源于肾上腺和肾上腺外嗜铬细胞。它们产生过量的儿茶酚胺及其代谢物。本研究建立了一种新的分析方法,采用半自动化微萃取技术(MEPS),结合数字控制注射器(eVol)和液相色谱-串联质谱法(LC-MS/MS),用于定量检测游离尿儿茶酚胺和甲氧基肾上腺素。评估了影响 MEPS 性能的重要参数,包括吸附剂材料(多孔石墨化碳(PGC)、极性增强聚合物(PEP)、阳离子交换(CX)和 C18)的类型、萃取循环次数和洗脱溶剂系统。实验的最佳条件为通过 C18 吸附剂在 MEPS 注射器中加载七个萃取循环的样品混合物,然后使用洗脱溶液(水/乙腈/甲酸,95/4.75/0.25)。整个样品制备过程大约需要 4 分钟。使用 HSS PFP 柱进行梯度洗脱可实现良好的色谱分离。方法的线性范围为肾上腺素 0.167-33.4ng/mL,去甲肾上腺素 0.650-130ng/mL,多巴胺 1.53-306ng/mL,甲氧基肾上腺素 1.34-268ng/mL,去甲变肾上腺素 3.43-686ng/mL,3-甲氧基酪胺 1.33-265ng/mL。日内和日间精密度均≤12.8%,相应的准确度分别为 88.4-112.0%和 89.0-109.5%。未酸化时的交叉污染和样品稳定性也进行了研究。使用临床尿液标本进行验证表明,与其他尿液生化检测相比,该方法具有更高的灵敏度。建立的 MEPS-LC-MS/MS 方法简单、快速、经济有效;有助于获得多种代谢物的信息。它适用于常规临床实验室中 PPGL 的筛查。