Degradation of copolymers obtained by ring-opening polymerization of glycolide and ε-caprolactone:: A high resolution NMR and ESI-MS study

Electrospray ionization-mass spectrometry (ESI-MS) and proton nuclear magnetic resonance (H-1 NMR) have been used to investigate the hydrolytic degradation of copolymers obtained by bulk ring-opening copolymerization of glycolide and epsilon-caprolactone with monomer ratios ranging from 70/30 to 30/70. NMR allows changes of the average sequence distribution and composition of the components to be followed. In contrast, ESI-MS is able to reveal the detailed chemical structures of various sequences despite the molecular weight limit of 2000 Da. Combination of ESI-MS with NMR can thus provide information to describe microstructure changes during degradation. The distribution of various oligomers shown in the form of planar projections is of great interest for the design of biodegradable system aimed at medical applications. (C) 2008 Elsevier Ltd. All rights reserved.