Simultaneous quantification of free fatty acids and acylcarnitines in plasma samples using dansylhydrazine labeling and liquid chromatography–triple quadrupole mass spectrometry

被引:0
作者
Guan-yuan Chen
Qibin Zhang
机构
[1] University of North Carolina at Greensboro,Center for Translational Biomedical Research
[2] National Taiwan University,Graduate Institute of Forensic Medicine
[3] University of North Carolina at Greensboro,Department of Chemistry & Biochemistry
来源
Analytical and Bioanalytical Chemistry | 2020年 / 412卷
关键词
Free fatty acid; Acylcarnitine; Chemical isotope labeling; LC-MRM-MS; Human plasma; Targeted metabolomics;
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摘要
Free fatty acid (FFA) and acylcarnitine (AcCar) are key elements of energy metabolism. Dysregulated levels of FFA and AcCar are associated with genetic defects and other metabolic disorders. Due to differences in the physicochemical properties of these two classes of compounds, it is challenging to quantify FFA and AcCar in human plasma using a single method. In this work, we developed a chemical isotope labeling (CIL)–based liquid chromatography–multiple reaction monitoring (LC-MRM) method to simultaneously quantify FFA and AcCar. Dansylhydrazine (DnsHz) was used to label the carboxylic acid moiety on FFA and AcCar. This resulted in the formation of a permanently charged ammonium ion for facile ionization in positive ionization mode and higher hydrophobicity for enhanced retention of short-chain analogs on reversed-phase LC columns and enabled absolute quantification by using heavy labeled DnsHz analogs as internal standards. Labeling conditions including the concentration and freshness of cross-linker, reaction time, and temperature were optimized. This method can successfully quantify all short-, medium- and long-chain FFAs and AcCars with greatly enhanced sensitivity. Using this method, 25 FFAs and 13 AcCars can be absolutely quantified and validated in human plasma samples within 12 min. Simultaneous quantification of FFA and AcCar enabled by this CIL-based LC-MRM method facilitates the investigation of fatty acid metabolism and has potential in clinical applications.
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页码:2841 / 2849
页数:8
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共 274 条
[1]  
Fritsche KL(2015)The science of fatty acids and inflammation Adv Nutr 6 293S-301S
[2]  
Simopoulos AP(2002)Omega-3 fatty acids in inflammation and autoimmune diseases J Am Coll Nutr 21 495-505
[3]  
Janssen CI(2014)Long-chain polyunsaturated fatty acids (LCPUFA) from genesis to senescence: the influence of LCPUFA on neural development, aging, and neurodegeneration Prog Lipid Res 53 1-17
[4]  
Kiliaan AJ(1994)Prospective study of plasma fatty acids and risk of prostate cancer J Natl Cancer Inst 86 281-286
[5]  
Gann PH(2006)Effects of omega-3 fatty acids on cancer risk: a systematic review JAMA 295 403-415
[6]  
Hennekens CH(2013)Omega-3 fatty acids prevent inflammation and metabolic disorder through inhibition of NLRP3 inflammasome activation Immunity 38 1154-1163
[7]  
Sacks FM(2009)Omega-3 polyunsaturated fatty acids and cardiovascular diseases J Am Coll Cardiol 54 585-594
[8]  
Grodstein F(2016)Carnitine transport and fatty acid oxidation Biochim Biophys Acta 1863 2422-2435
[9]  
Giovannucci EL(1997)Rapid diagnosis of MCAD deficiency: quantitative analysis of octanoylcarnitine and other acylcarnitines in newborn blood spots by tandem mass spectrometry Clin Chem 43 2106-2113
[10]  
Stampfer MJ(2018)Disorders of mitochondrial long-chain fatty acid oxidation and the carnitine shuttle Rev Endocr Metab Disord 19 93-106