Development of a simultaneous quantitation for short-, medium-, long-, and very long-chain fatty acids in human plasma by 2-nitrophenylhydrazine-derivatization and liquid chromatography-tandem mass spectrometry

被引:25
作者
Chen, Zhen [1 ]
Gao, Zijun [1 ]
Wu, Yue [1 ]
Shrestha, Rojeet [1 ]
Imai, Hiromitsu [2 ]
Uemura, Naoto [3 ]
Hirano, Ken-ichi [4 ,5 ]
Chiba, Hitoshi [6 ]
Hui, Shu-Ping [1 ]
机构
[1] Hokkaido Univ, Fac Hlth Sci, Kita Ku, Kita 12,Nishi 5, Sapporo, Hokkaido 0600812, Japan
[2] Oita Univ Hosp, Clin Pharmacol Ctr, Oita 8795503, Japan
[3] Oita Univ, Dept Clin Pharmacol & Therapeut, Fac Med, Oita 8795503, Japan
[4] Osaka Univ, Grad Sch Med, Lab Cardiovasc Dis Novel Noninvas & Nutr Therapeu, Osaka 5650874, Japan
[5] Osaka Univ, Grad Sch Med, Dept Cardiovasc Med, Osaka 5650874, Japan
[6] Sapporo Univ Hlth Sci, Dept Nutr, Higashi Ku, Nakanuma Nishi 4-2-1-15, Sapporo, Hokkaido 0070894, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2019年 / 1126卷
关键词
Fatty acid; LC-MS/MS; 2-Nitrophenylhydrazine; Derivatization; Plasma; GAS-CHROMATOGRAPHY; MS METHOD; DERIVATIZATION; BLOOD; QUANTIFICATION; PROFILE;
D O I
10.1016/j.jchromb.2019.121771
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fatty acids (FA) have been important in clinical diagnosis for long, which makes the increasing need for a fast, reliable, and economic approach to determine FA of short-, medium-, long-, and very long-chain by widely available equipment and with high-throughput capacity. In the present work, 2-nitrophenylhydrazine derivatization coupling with LC-MS/MS detection was utilized to simultaneously quantitate 18 FAs ranging from C4 to C26 in human plasma. The sample preparation protocol was optimized and extracting with diethyl ether-potassium phosphate buffer twice was found as the highest efficiency along with economic feasibility. Under the optimized conditions, all the FA showed excellent linearity (R-2 > 0.999 for each), sufficient sensitivity (LOD 0.2-330 fmol and LOQ 2.3-660 fmol for all), favorable accuracy (recovery ranged from 98.1 +/- 3.6% to 104.9 +/- 5.5% with coefficient of variation no > 8.6% for all), and negligible matrix effect. In the clinical application on 30 healthy subjects, compared with the previous HPLC-UV method, the developed method showed high reliability, as well as reduced time and reagent costs. The established method showed the potential to apply to not only diagnostic practice, but also nutritional and epidemiological studies.
引用
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页数:8
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