Measurement of the malondialdehyde-2′-deoxyguanosine adduct in human urine by immunoextraction and liquid chromatography/atmospheric pressure chemical ionization tandem mass spectrometry

被引:42
作者
Hoberg, AM
Otteneder, M
Marnett, LJ
Poulsen, HE
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Clin Pharmacol, DK-2100 Copenhagen O, Denmark
[2] Vanderbilt Univ, Sch Med, Vanderbilt Canc Ctr,Dept Biochem, AB Hancock Jr Mem Lab,Canc Res Ctr Mol Toxicol, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Vanderbilt Canc Ctr,Dept Chem, AB Hancock Jr Mem Lab,Canc Res Ctr Mol Toxicol, Nashville, TN 37232 USA
[4] Bayer AG, Preclin Pharmacokinet, PH PD P PPK, D-42096 Wuppertal, Germany
来源
JOURNAL OF MASS SPECTROMETRY | 2004年 / 39卷 / 01期
关键词
atmospheric pressure chemical ionization; liquid chromatography/tandem mass spectrometry; lipid peroxidation; biomarker; DNA adducts; malondialdehyde;
D O I
10.1002/jms.547
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The major adduct of malondialdehyde with guanine, M(1)G, was measured in human urine from nonsmoking healthy individuals. M(1)G is a mutagenic DNA lesion and a terminal product of lipid peroxidation in vivo that may be implicated in cancer related to lifestyle and diet. On the basis of a recently developed method for the quantification of M(1)G as an excreted deoxynucleoside using immuno-extraction purification, chemical NaBH4 reduction and liquid chromatography combined with atmospheric pressure chemical ionization tandem mass spectrometry, we demonstrate that the average 24 h excretion rate of M(1)G-dR is about 12+/-3.8 fmol kg(-1) (n = 5). Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:38 / 42
页数:5
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