Ouyang Yilan, Wu Chengling, Sun Xue, Liu Jianfen, Linhardt Robert J, Zhang Zhenqing
Jiangsu Key Laboratory of Translational Research and Therapy for Neuro-Psycho-Diseases and College of Pharmaceutical Sciences, Soochow University, Suzhou, Jiangsu, 215021, China.
Xiehe Pharmaceutical Co. Ltd, Shijiazhuang, Hebei Province, 050083, China.
Rapid Commun Mass Spectrom. 2016 Jan 30;30(2):277-84. doi: 10.1002/rcm.7437.
Heparin and low molecular weight heparin (LMWH) are widely used as clinical anticoagulants. The determination of their composition and structural heterogeneity still challenges analysts.
Disaccharide compositional analysis, utilizing heparinase-catalyzed depolymerization, is one of the most important ways to evaluate the sequence, structural composition and quality of heparin and LMWH. Hydrophilic interaction chromatography coupled with quadruple time-of-flight mass spectrometry (HILIC/QTOFMS) has been developed to analyze the resulting digestion products.
HILIC shows good resolution and excellent MS compatibility. Digestion products of heparin and LMWHs afforded up to 16 compounds that were separated using HILIC and analyzed semi-quantitatively. These included eight common disaccharides, two disaccharides derived from chain termini, three 3-O-sulfo-group-containing tetrasaccharides, along with three linkage region tetrasaccharides and their derivatives. Structures of these digestion products were confirmed by mass spectral analysis. The disaccharide compositions of a heparin, two batches of the LMWH, enoxaparin, and two batches of the LMWH, nadroparin, were compared. In addition to identifying disaccharides, 3-O-sulfo-group-containing tetrasaccharides, linkage region tetrasaccharides were observed having slightly different compositions and contents in these heparin products suggesting that they had been prepared using different starting materials or production processes.
Thus, compositional analysis using HILIC/QTOFMS offers a unique insight into different heparin products.
肝素和低分子量肝素(LMWH)作为临床抗凝剂被广泛使用。其成分和结构异质性的测定仍然是分析人员面临的挑战。
利用肝素酶催化解聚进行二糖组成分析,是评估肝素和低分子量肝素序列、结构组成及质量的最重要方法之一。亲水相互作用色谱联用四极杆飞行时间质谱(HILIC/QTOFMS)已被开发用于分析所得消化产物。
HILIC显示出良好的分离度和出色的质谱兼容性。肝素和低分子量肝素的消化产物产生了多达16种化合物,这些化合物通过HILIC分离并进行了半定量分析。其中包括8种常见二糖、2种源自链端的二糖、3种含3-O-磺基的四糖,以及3种连接区四糖及其衍生物。这些消化产物的结构通过质谱分析得以确认。对一种肝素、两批低分子量肝素依诺肝素以及两批低分子量肝素那屈肝素的二糖组成进行了比较。除了鉴定二糖外,还观察到这些肝素产品中含3-O-磺基的四糖、连接区四糖的组成和含量略有不同,这表明它们是使用不同的起始原料或生产工艺制备的。
因此,使用HILIC/QTOFMS进行组成分析为不同的肝素产品提供了独特的见解。