TY - JOUR
T1 - A chemiluminescence method to detect malondialdehyde in plasma and urine
AU - Zhang, Guangbin
AU - Tang, Yuhai
AU - Shi, Xiaoyu
AU - Gao, Ruixia
AU - Sun, Yang
AU - Du, Wei
AU - Fu, Qiang
PY - 2013
Y1 - 2013
N2 - A highly sensitive and convenient method to detect malondialdehyde (MDA) in specimens of plasma and urine was developed using high-performance liquid chromatography combining chemiluminescence detection. MDA was separated through a reverse-phase C18 column at a flow rate of 0.8 ml min-1. It was then detected by a chemiluminescence detector. Variables that affected chemiluminescence reaction, including mobile phase, flow rate, chemiluminescence reagent, parameters of the photomultiplier tube, and temperature, were studied. This assay was linear from 0.50 to 50 μmol L-1, with limits of detection and quantification of 0.08 and 0.30 μmol L-1, respectively. The recoveries were in the range of 92.2 to 98.5%, and the intra- and interday reproducibilities were obtained with relative standard deviations of less than 4% and less than 6%, respectively. MDA in plasma and urine was stable for 12 h at 4 C. MDA levels were 2.74, 3.19, and 3.20 μmol L -1 for plasma and 1.25, 2.04, and 1.58 μmol L-1 for urine, respectively. The proposed method is simple, rapid, and sensitive with low cost. Taken together, this method can be suitable for detecting MDA in tissue and feed specimens.
AB - A highly sensitive and convenient method to detect malondialdehyde (MDA) in specimens of plasma and urine was developed using high-performance liquid chromatography combining chemiluminescence detection. MDA was separated through a reverse-phase C18 column at a flow rate of 0.8 ml min-1. It was then detected by a chemiluminescence detector. Variables that affected chemiluminescence reaction, including mobile phase, flow rate, chemiluminescence reagent, parameters of the photomultiplier tube, and temperature, were studied. This assay was linear from 0.50 to 50 μmol L-1, with limits of detection and quantification of 0.08 and 0.30 μmol L-1, respectively. The recoveries were in the range of 92.2 to 98.5%, and the intra- and interday reproducibilities were obtained with relative standard deviations of less than 4% and less than 6%, respectively. MDA in plasma and urine was stable for 12 h at 4 C. MDA levels were 2.74, 3.19, and 3.20 μmol L -1 for plasma and 1.25, 2.04, and 1.58 μmol L-1 for urine, respectively. The proposed method is simple, rapid, and sensitive with low cost. Taken together, this method can be suitable for detecting MDA in tissue and feed specimens.
KW - High-performance liquid chromatography-chemiluminescence
KW - Malondialdehyde
KW - Plasma
KW - Urine
UR - https://www.scopus.com/pages/publications/84884526725
U2 - 10.1016/j.ab.2013.08.011
DO - 10.1016/j.ab.2013.08.011
M3 - 文章
C2 - 23973627
AN - SCOPUS:84884526725
SN - 0003-2697
VL - 443
SP - 16
EP - 21
JO - Analytical Biochemistry
JF - Analytical Biochemistry
IS - 1
ER -