Analytical method for the determination of disaccharides derived from keratan, heparan, and dermatan sulfates in human serum and plasma by high-performance liquid chromatography/turbo ionspray ionization tandem mass spectrometry
Analytical method for the determination of disaccharides derived from keratan, heparan, and dermatan sulfates in human serum and plasma by high-performance liquid chromatography/turbo ionspray ionization tandem mass spectrometry
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DOI:
10.1016/j.ab.2007.05.016
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发表时间:
2007-09-01
影响因子:
2.9
通讯作者:
Okazaki, Osamu
中科院分区:
文献类型:
--
作者:
Oguma, Toshihiro;Tomatsu, Shunji;Okazaki, Osamu
We established a highly sensitive liquid chromatography tandem mass spectrometry (LC-MS/MS) method to analyze the disaccharides produced from keratan sulfate (KS), heparan sulfate (HS), and dermatan sulfate (DS). It was revealed that KS, HS, and DS in human serum and plasma were digested to each disaccharide by keratanase 11, heparitinase, and chondroitinase 13, respectively. Analysis of disaccharides was performed by LC-MS/MS with multiple reactions monitoring in the negative ion mode. Separation of LC was performed on a Hypercarb (2.0 mm i.d. x 150 mm, 5 mu m) with a gradient elution of acetonitrile-0.01 M ammonium bicarbonate (pH 10). The mobile phase flow rate was 0.2 ml/min. An API-4000 mass spectrometer equipped with a turbo ionspray was used to determine each glycosaminoglycan (GAG) in the serum of control subjects and plasma of muco polysaccharidose (NIPS) patients. The intraday precision expressed as a coefficient of variation was within 15.80/0 for five replicate analyses with three human control samples. The interclay (overall, n = 15) precision was within 14.8% for 3 days. This method is sensitive and reproducible, and it would be useful for clinical diagnosis. (c) 2007 Elsevier Inc. All rights reserved.