Fluorescence determination of N-acetylaspartic acid in the rat cerebrum homogenate using high-performance liquid chromatography with pre-column fluorescence derivatization

被引:9
|
作者
Fukushima, Takeshi [1 ]
Arai, Kotaro [1 ]
Tomiya, Masayuki [1 ]
Mitsuhashi, Shogo [1 ]
Sasaki, Tsukasa [1 ]
Santa, Tomofumi [2 ]
Imai, Kazuhiro [3 ]
Toyo'oka, Toshimasa [1 ]
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Div Bioanalyt Chem, Suruga Ku, Shizuoka 4228526, Japan
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Bioanalyt Chem, Tokyo 1130033, Japan
[3] Musashino Univ, Res Inst Pharmaceut Sci, Tokyo 2028585, Japan
关键词
N-Acetyl-L-aspartic acid; HPLC; DBD-ED; rat cerebrum homogenate; fluorescence detection;
D O I
10.1002/bmc.902
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
N-Acetyl-L-aspartic acid (NAA) is an endogenous compound, and its brain concentration is suggested to be altered in neurological disorders. In the present study, a fluorescence determination method for NAA was developed by employing reversed-phase high-performance liquid chromatography (HPLC) with pre-column fluorescence derivatization using 4-N,N-dimethylaminosulfonyl-7-N-(2-aminoethyl)amino-2,1,3-benzoxadiazole (DBD-ED). Using methylsuccinic acid as the internal standard, a linear calibration curve for NAA was constructed in the range 125-1000 mu m (n = 3). The detection limit on the column was approximately 5.0 fmol (signal-to-noise ratio 3). The proposed HPLC method was applied to determine NAA in the rat cerebrum homogenate. Cerebrum NAA was successfully determined using 10 mu L of the homogenate, and the validation data for the proposed HPLC method demonstrated satisfactory results. Intra- and inter-day precision and accuracy were within 1.1-7.0 and -8.1-6.3%, respectively. The concentration of NAA in the male rat cerebrum (13 weeks old) was 84 +/- 4.6 mu mol/mg protein (n 3). Copyright (c) 2007 John Wiley & Sons, Ltd.
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页码:100 / 105
页数:6
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