Dried blood spot (DBS) sample collection for determination of the oxidative stress biomarker 8-epi-PGF2a in humans using liquid chromatography/tandem mass spectrometry

被引:15
作者
Bastani, Nasser E. [1 ]
Gundersen, Thomas E. [1 ,2 ]
Blomhoff, Rune [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, N-0316 Oslo, Norway
[2] Vitas AS, N-0349 Oslo, Norway
关键词
HUMAN URINE; ISOPROSTANES; VALIDATION; PRODUCTS; F-2-ISOPROSTANES; QUANTITATION; EXTRACTION; SMOKERS; ACID;
D O I
10.1002/rcm.6149
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RATIONALE: F2-isoprostanes are a series of prostaglandin F2-like compounds that are formed by free-radical-catalyzed peroxidation of arachidonic acid (ARA). Several F2-isoprostanes, but in particular 8-epi-PGF(2 alpha), are widely used as oxidative stress biomarkers. In this study we have developed an analytical tool for finger-tip blood sampling and analysis of 8-epi-PGF(2 alpha) from dried blood spots (DBS). METHODS: We have applied solid-phase extraction (SPE) and liquid chromatography/tandem mass spectrometry (LC/MS/ MS) for the extraction, separation and detection of 8-epi-PGF(2 alpha) in DBS and have studied the stability of this marker using the DBS collection platform. RESULTS: The mass limit of detection (mLOD) for 8-epi-PGF(2 alpha) extracted from DBS samples was 1.5 pg while the concentration limit of detection (cLOD) and concentration limit of quantitation (cLOQ) were 6 pg/mL and 18 pg/mL, respectively. All values based on triplicate analysis. Sufficient stability of 8-epi-PGF(2 alpha) in DBS was achieved by preconditioning DBS paper with vitamin E and BHT. CONCLUSIONS: The developed method is sensitive, specific, robust, efficient, and can accurately measure endogenous concentrations of 8-epi-PGF2a in DBS. Thus, it offers an analytical approach to measure 8-epi-PGF2a by a novel sample collection technique that is less invasive and costly than conventional techniques. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:645 / 652
页数:8
相关论文
共 31 条
[21]   Measurement of F2-isoprostanes as an index of oxidative stress in vivo [J].
Roberts, LJ ;
Morrow, JD .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (04) :505-513
[22]   Total synthesis of isoprostanes:: discovery and quantitation in biological systems [J].
Rokach, J ;
Kim, S ;
Bellone, S ;
Lawson, JA ;
Praticò, D ;
Powell, WS ;
FitzGerald, GA .
CHEMISTRY AND PHYSICS OF LIPIDS, 2004, 128 (1-2) :35-56
[23]   Pre-radiotherapy plasma carotenoids and markers of oxidative stress are associated with survival in head and neck squamous cell carcinoma patients: A prospective study [J].
Sakhi A.K. ;
Russnes K.M. ;
Thoresen M. ;
Bastani N.E. ;
Karlsen A. ;
Smeland S. ;
Blomhoff R. .
BMC Cancer, 9 (1)
[24]  
Samuelsson G., 1992, DRUGS NATURAL ORIGIN, P171
[25]   Isoprostane measurement in plasma and urine by liquid chromatography-mass spectrometry with one-step sample preparation [J].
Sircar, Debajit ;
Subbaiah, Papasani V. .
CLINICAL CHEMISTRY, 2007, 53 (02) :251-258
[26]   Dried Blood Spots as a Sample Collection Technique for the Determination of Pharmacokinetics in Clinical Studies: Considerations for the Validation of a Quantitative Bioanalytical Method [J].
Spooner, Neil ;
Lad, Rakesh ;
Barfield, Matt .
ANALYTICAL CHEMISTRY, 2009, 81 (04) :1557-1563
[27]   Women and smokers have elevated urinary F2-isoprostane metabolites:: A novel extraction and LC-MS methodology [J].
Taylor, Alan W. ;
Bruno, Richard S. ;
Traber, Maret G. .
LIPIDS, 2008, 43 (10) :925-936
[28]  
Wu TY, 2004, CANCER EPIDEM BIOMAR, V13, P1399
[29]   Quantitation of isoprostane isomers in human urine from smokers and nonsmokers by LC-MS/MS [J].
Yan, Weiying ;
Byrd, Gary D. ;
Ogden, Michael W. .
JOURNAL OF LIPID RESEARCH, 2007, 48 (07) :1607-1617
[30]   Simultaneous measurement of F2-isoprostane, hydroxyoctadecadienoic acid, hydroxyeicosatetraenoic acid, and hydroxycholesterols from physiological samples [J].
Yoshida, Yasukazu ;
Kodai, Shintaro ;
Takemura, Shigekazu ;
Minamiyama, Yukiko ;
Niki, Etsuo .
ANALYTICAL BIOCHEMISTRY, 2008, 379 (01) :105-115