High-performance liquid chromatography/electrospray ionization tandem mass spectrometry for characterization of enzymatic degradation of 2.2′-bis(2-oxazoline)-linked poly-ε-caprolactone

被引:12
|
作者
Pulkkinen, Mika [1 ]
Palmgren, Joni J. [1 ]
Auriola, Seppo [2 ]
Malin, Minna [3 ]
Seppala, Jukka [3 ]
Jarvinen, Kristiina [1 ]
机构
[1] Univ Kuopio, Dept Pharmaceut, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Pharmaceut Chem, FIN-70211 Kuopio, Finland
[3] Aalto Univ, Dept Chem Technol, Lab Polymer Technol, FIN-02015 Helsinki, Finland
关键词
D O I
10.1002/rcm.3336
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper describes a straightforward and rapid on-line characterization using high-performance liquid chromatography/electrospray ionization tandem mass spectrometry (HPLC/ESI-MSn) of the enzymatic degradation products of 2,2'-bis(2-oxazoline)-linked poly-epsilon-caprolactone (PCL-O). These new PCL-O polymers are expected to be used in a variety of pharmaceutical and biomedical applications since they are degraded enzymatically by surface erosion. PCL-O was polymerized in a three-step reaction and characterized by H-1-NMR and size-exclusion chromatography (SEC). Solvent cast polymer films were exposed to enzymatic degradation in phosphate buffer (pH 7.5, 1% pancreatin). The enzymatic degradation of the polymer produced a wide variety of water-soluble oligomers which were separated and identified by HPLC/ESI-MSn. Optimization of the gradient HPLC method resulted in effective separation of the oligomers. Furthermore, specific structures of the oligomers were clearly identified by tandem mass spectrometry. According to these results, ester bonds seem to be most sensitive to enzymatic degradation and, correspondingly, pancreatic lipase seems to be mainly responsible for the enzymatic erosion of the PCL-O films. This novel mass spectrometric method provides important knowledge about the enzymatic degradation process and structure of the polymer which is difficult to ascertain by other conventional methods. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:121 / 129
页数:9
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