Stable-isotope dilution LC-MS for quantitative biomarker analysis

被引:158
作者
Ciccimaro, Eugene [3 ]
Blair, Ian A. [1 ,2 ]
机构
[1] Univ Penn, Dept Pharmacol, Sch Med, Ctr Excellence Environm Toxicol, 421 Curie Blvd, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Pharmacol, Sch Med, Ctr Canc Pharmacol, Philadelphia, PA 19104 USA
[3] Thermo Fisher Sci, Somerset, NJ 08873 USA
关键词
OXIDATIVE DNA-DAMAGE; TANDEM MASS-SPECTROMETRY; MONOCYTE CHEMOATTRACTANT PROTEIN-1; CHIRAL LIPIDOMICS ANALYSIS; PROSTATE-SPECIFIC ANTIGEN; LIQUID-CHROMATOGRAPHY; ELECTROSPRAY-IONIZATION; ABSOLUTE QUANTIFICATION; BREAST-CANCER; HUMAN SERUM;
D O I
10.4155/BIO.09.185
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The ability to conduct validated analyses of biomarkers is critically important in order to establish the sensitivity and selectivity of the biomarker in identifying a particular disease. The use of stable-isotope dilution (SID) methodology in combination with LC-MS/MS provides the highest possible analytical specificity for quantitative determinations. This methodology is now widely used in the discovery and validation of putative exposure and disease biomarkers. This review will describe the application of SID LC-MS methodology for the analysis of small-molecule and protein biomarkers. It will also discuss potential future directions for the use of this methodology for rigorous biomarker analysis.
引用
收藏
页码:311 / 341
页数:31
相关论文
共 248 条
[151]   Human biochemistry of the isoprostane pathway [J].
Milne, Ginger L. ;
Yin, Huiyong ;
Morrow, Jason D. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (23) :15533-15537
[152]   Comparative evaluation of current peptide production platforms used in absolute quantification in proteomics [J].
Mirzaei, Hamid ;
McBee, Joshua K. ;
Watts, Julian ;
Aebersold, Ruedi .
MOLECULAR & CELLULAR PROTEOMICS, 2008, 7 (04) :813-823
[153]   Folate and homocysteine phenotypes: Comparative findings using research and clinical laboratory data [J].
Mitchell, Laura E. ;
Morales, Megan ;
Khartulyari, Stefanie ;
Huang, Yuehua ;
Murphy, Kristen ;
Mei, Minghua ;
Von Feldt, Joan M. ;
Blair, Ian A. ;
Whitehead, Alexander S. .
CLINICAL BIOCHEMISTRY, 2009, 42 (12) :1275-1281
[154]   Insights into oxidative stress: The isoprostanes [J].
Montuschi, Paolo ;
Barnes, Peter ;
Jackson Roberts, L. .
CURRENT MEDICINAL CHEMISTRY, 2007, 14 (06) :703-717
[155]   The isoprostanes - Unique products of arachidonate peroxidation: Their role as mediators of oxidant stress [J].
Morrow, JD .
CURRENT PHARMACEUTICAL DESIGN, 2006, 12 (08) :895-902
[156]  
MUCHMORE DC, 1989, METHOD ENZYMOL, V177, P44
[157]   Electrospray ionization and tandem mass spectrometry of eicosanoids [J].
Murphy, RC ;
Barkley, RM ;
Berry, KZ ;
Hankin, J ;
Harrison, K ;
Johnson, C ;
Krank, J ;
McAnoy, A ;
Uhlson, C ;
Zarini, S .
ANALYTICAL BIOCHEMISTRY, 2005, 346 (01) :1-42
[158]   Glutathione adducts of oxyeicosanoids [J].
Murphy, RC ;
Zarini, S .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2002, 68-9 :471-482
[159]   Recent advances in the biochemistry and clinical relevance of the isoprostane pathway [J].
Musiek, ES ;
Yin, HY ;
Milne, GL ;
Morrow, JD .
LIPIDS, 2005, 40 (10) :987-994
[160]   Oxidative damage in nucleic acids and Parkinson's disease [J].
Nakabeppu, Yusaku ;
Tsuchimoto, Daisuke ;
Yamaguchi, Hiroo ;
Sakumi, Kunihiko .
JOURNAL OF NEUROSCIENCE RESEARCH, 2007, 85 (05) :919-934