Abstract
Malondialdehyde (MDA) is one of the most commonly reported biomarkers of lipid peroxidation in clinical studies. The reaction of thiobarbituric acid (TBA) with MDA to yield a pink chromogen attributable to an MDA-TBA 2 adduct is a common assay approach with products being quantified by ultraviolet-Vis assay as nonspecific TBAreactive substances (TBARS) or chromatographically as MDA. The specifi city of the TBARS assay was compared with both chromatographic assays for total plasma MDA. The levels of total plasma MDA were signifi cantly lower than the plasma TBARS in each of the samples examined, and interestingly, the interindividual variation apparent in the level of plasma MDA was not evident in the plasma TBARS assay. Each of the four online chromatographic detectors yielded a precise, sensitive, and accurate determination of total plasma MDA, and selected-ion monitoring was the most-accurate assay (101.3%, n = 4). The online diode array detectors provided good assay specifi city (peak purity index of 999), sensitivity, precision, and accuracy. This research demonstrates the inaccuracy that is inherent in plasma TBARS assays, which claim to quantify MDA, and it is proposed that the TBARS approach may limit the likelihood of detecting true differences in the level of lipid peroxidation in clinical studies
Original language | English |
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Pages (from-to) | 852-858 |
Number of pages | 7 |
Journal | Journal of Lipid Research |
Volume | 54 |
Issue number | 3 |
DOIs | |
Publication status | Published - Mar 2013 |
Externally published | Yes |
Keywords
- Assay specifi city assay bias lipid peroxidation
- High-performance liquid chromatography
- Thiobarbituric acid-reactive substance
ASJC Scopus subject areas
- Biochemistry
- Endocrinology
- Cell Biology