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UPLC-ESI-MS/MS 法测定人尿中脂肪族二胺、氧化三甲胺和 β-甲基氨基-l-丙氨酸

UPLC-ESI-MS/MS method for the quantitative measurement of aliphatic diamines, trimethylamine N-oxide, and β-methylamino-l-alanine in human urine.

机构信息

Centers for Disease Control and Prevention, Division of Laboratory Sciences, Tobacco and Volatiles Branch, Atlanta, GA 30341, United States.

Centers for Disease Control and Prevention, Division of Laboratory Sciences, Tobacco and Volatiles Branch, Atlanta, GA 30341, United States.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2018 Apr 15;1083:86-92. doi: 10.1016/j.jchromb.2018.02.043. Epub 2018 Mar 2.

Abstract

This work describes a quantitative high-throughput analytical method for the simultaneous measurement of small aliphatic nitrogenous biomarkers, i.e., 1,6-hexamethylenediamine (HDA), isophoronediamine (IPDA), β-methylamino-l-alanine (BMAA), and trimethylamine N-oxide (TMAO), in human urine. Urinary aliphatic diamines, HDA and IPDA, are potential biomarkers of environmental exposure to their corresponding diisocyanates. Urinary BMAA forms as a result of human exposure to blue-green algae contaminated food. And, TMAO is excreted in urine due to the consumption of carnitine- and choline-rich diets. These urinary biomarkers represent classes of small aliphatic nitrogen-containing compounds (N-compounds) that have a high aqueous solubility, low logP, and/or high basic pK. Because of the highly polar characteristics, analysis of these compounds in complex sample matrices is often challenging. We report on the development of ion-pairing chemistry based ultra-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS) method for the simultaneous measurement of these biomarkers in human urine. Chromatographic separation was optimized using heptafluorobutyric acid-(HFBA-) based mobile phase and a reversed-phase C18 column. All four analytes were baseline separated within 2.6 min with an overall run time of 5 min per sample injection. Sample preparation involved 4 h of acid hydrolysis followed by automated solid phase extraction (SPE) performed using strong cation exchange sorbent bed with 7 N ammonia solution in methanol as eluent. Limits of detection ranged from 0.05 ng/mL to 1.60 ng/mL. The inter-day and intra-day accuracy were within 10%, and reproducibility within 15%. The method is accurate, fast, and well-suited for biomonitoring studies within targeted groups, as well as larger population-based studies such as the U. S. National Health and Nutrition Examination Survey (NHANES).

摘要

本工作描述了一种定量高通量分析方法,用于同时测量小脂肪族含氮生物标志物,即 1,6-己二胺(HDA)、异佛尔酮二胺(IPDA)、β-甲基氨基-l-丙氨酸(BMAA)和氧化三甲胺(TMAO),在人尿中。尿中脂肪族二胺,HDA 和 IPDA,是其相应二异氰酸酯环境暴露的潜在生物标志物。尿中 BMAA 是由于人类暴露于受蓝绿藻污染的食物而形成的。并且,由于食用富含肉碱和胆碱的饮食,TMAO 会随尿液排出。这些尿生物标志物代表了一类具有高水溶性、低 logP 和/或高碱性 pK 的小脂肪族含氮化合物(N 化合物)。由于其高度极性的特点,分析这些化合物在复杂的样品基质中常常具有挑战性。我们报告了基于离子对化学的超高效液相色谱-电喷雾电离-串联质谱(UPLC-ESI-MS/MS)方法的发展,用于同时测量人尿中的这些生物标志物。采用基于七氟丁酸(HFBA)的流动相和反相 C18 柱对色谱分离进行了优化。所有四种分析物在 2.6 分钟内实现基线分离,每个样品进样的总运行时间为 5 分钟。样品制备涉及 4 小时的酸水解,然后使用强阳离子交换固相萃取(SPE),用甲醇中的 7N 氨溶液作为洗脱剂。检测限范围为 0.05ng/mL 至 1.60ng/mL。日间和日内准确度在 10%以内,重复性在 15%以内。该方法准确、快速,非常适合于目标人群的生物监测研究,以及更大规模的基于人群的研究,如美国国家健康和营养检查调查(NHANES)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/541e/7919444/5461435985e1/nihms-1672246-f0002.jpg

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