4.5 Article

Concurrent quantification of multiple biomarkers indicative of oxidative stress status using liquid chromatography-tandem mass spectrometry

期刊

ANALYTICAL BIOCHEMISTRY
卷 512, 期 -, 页码 26-35

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2016.07.030

关键词

Oxidative stress; Urine; Biomarkers; Isotope dilution; Liquid chromatography-tandem mass spectrometry

资金

  1. National Taiwan University [102R7622-6]
  2. Environmental Medicine Collaboration Center (EMC2)
  3. National Taiwan University Hospital, Taiwan (NTUH) [103-A123]

向作者/读者索取更多资源

8-Hydroxy-2-deoxyguanosine (8-OHdG), 8-nitroguanine (8-NO(2)Gua), 8-iso-prostaglandin F-2 alpha (8-IsoPGF(2 alpha)), and N-acetyl-S-(tetrahydro-5-hydroxy-2-pentyl-3-furanyl)-L-cysteine (HNE-MA) are well studied and representative biomarkers for oxidative DNA damage, inflammation, and lipid peroxidation; all of which have been associated with increases in risks of various diseases and cancers. A rapid and highly sensitive isotope-dilution liquid-chromatography tandem mass spectrometry (LC-MS/MS) method was developed to simultaneously quantify the aforementioned biomarkers in urine. Upon validation, this method shows excellent feasibility, sensitivity (0.008-0.03 ng/mL) and satisfactory recoveries (88.7-95.4%); the calibration curves displayed excellent linearity with coefficients of determination (R-2) greater than 0.998. Additionally, low variations were observed in the relative standard deviation for intra- and inter-day measurements for the four analytes. The relative matrix effects for all four analytes ranged from 2.04 to 3.27%, which signaled that interferences from endogenous levels of the analytes were deemed statistically insignificant. This study successfully developed an analytical method capable to simultaneously quantify urinary 8-OHdG, 8-NO2Gua, 8-IsoPGF(2 alpha), and HNE-MA. This analytical protocol can be applied towards conducting epidemiological studies to reveal the mechanisms related to disease development, and thus evaluate the associated risks of diseases. (C) 2016 Elsevier Inc. All rights reserved.

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