Pfizer Global Research and Development, Cambridge Laboratories, Pfizer, Inc., Cambridge, Massachusetts 02139, United States.
Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.
J Am Soc Mass Spectrom. 2020 Mar 4;31(3):498-507. doi: 10.1021/jasms.9b00076. Epub 2020 Jan 28.
Acylcarnitines have been identified in human and animal metabolomic-profiling studies as urinary markers of radiation exposure, a result which is consistent with their cytoprotective effects and roles in energy metabolism. In the present work, a rapid method for quantitation of the more abundant acylcarnitines in human urine is developed using a valuable set of samples from cancer patients who received total body irradiation (TBI) at Memorial Sloan Kettering Cancer Center. The method uses solid-phase extraction (SPE) processing followed by differential mobility spectrometry (DMS with ethyl acetate modifier) tandem mass spectrometry (ESI-DMS-MS/MS) with deuterated internal standards. The analyzed human urine samples were collected from 38 individual patients at three time points over 24 h during and after the course of radiation treatment, a design allowing each patient to act as their own control and creatinine normalization. Creatinine-normalized concentrations for nine urinary acylcarnitine (acyl-CN) species are reported. Six acyl-CN species were reduced at the 6 h point. Acetylcarnitine (C2:0-CN) and valerylcarnitine (C5:0-CN) showed recovery at 24 h, but none of the other acyl-CN species showed recovery at that point. Levels of three acyl-CN species were not significantly altered by radiation. This rapid quantitative method for clinical samples covers the short- and medium-chain acylcarnitines and has the flexibility to be expanded to cover additional radiation-linked metabolites. The human data presented here indicates the utility of the current approach as a rapid, quantitative technique with potential applications by the medical community, by space research laboratories concerned with radiation exposure, and by disaster response groups.
酰基辅酶 A 在人类和动物代谢组学研究中被确定为辐射暴露的尿液标志物,这一结果与它们的细胞保护作用和在能量代谢中的作用一致。在本工作中,开发了一种快速定量人尿液中更丰富酰基辅酶 A 的方法,该方法使用 Memorial Sloan Kettering 癌症中心接受全身照射 (TBI) 的癌症患者的一组有价值的样本。该方法使用固相萃取 (SPE) 处理,然后使用差分式迁移率光谱 (DMS 与乙酸乙酯修饰剂) 串联质谱 (ESI-DMS-MS/MS) 和氘代内标进行分析。所分析的人类尿液样本来自 38 名个体患者,在辐射治疗过程中和之后的 24 小时内的三个时间点收集,设计允许每个患者作为自己的对照和肌酐归一化。报告了九种尿酰基辅酶 A (酰基-CN) 物种的肌酐归一化浓度。六种酰基-CN 物种在 6 小时点减少。乙酰基辅酶 A (C2:0-CN) 和缬基基辅酶 A (C5:0-CN) 在 24 小时时恢复,但其他酰基-CN 物种在该时间点均未恢复。三种酰基-CN 物种的水平未因辐射而显著改变。这种用于临床样本的快速定量方法涵盖了短链和中链酰基辅酶 A,并且具有灵活性,可以扩展到涵盖其他与辐射相关的代谢物。这里呈现的人类数据表明,当前方法具有作为一种快速、定量技术的实用性,具有潜在的应用价值,可用于医疗界、关注辐射暴露的空间研究实验室和灾难应对小组。