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Updated: Oct 10, 2026

Characterization of Synthetic Polymers via Matrix Assisted Laser Desorption Ionization Time of Flight (MALDI-TOF) Mass Spectrometry
Published on: June 10, 2018
End-group-selective size-exclusion chromatography-mass spectrometry of poly(lactic acid) and
Masashi Serizawa1, Rick van den Hurk2, Stefan van Berkel3
1Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, the Netherlands; Centre for Analytical Sciences Amsterdam, Science Park 904, Amsterdam, 1098 XH, the Netherlands; Material Characterization Laboratory, Mitsubishi Chemical Corporation, 1000 Kamoshida-cho, Aoba-ku, Yokohama-shi, Kanagawa, 227-8502, Japan.
Abstract:
End-group-selective size-exclusion chromatography (esSEC) coupled with mass spectrometry (MS) is presented as an analytical approach for the separation and characterization of acid-terminated and non-acid-terminated poly(lactic acid) (PLA) and poly(lactide-co-glycolide) (PLGA). The method uses a gradient normal-phase liquid chromatography system with basic (triethylamine) and acidic (formic acid) additives in ethyl acetate-based mobile phases, enabling selective retention of acid-terminated polymers, while non-acid-terminated species elute according to hydrodynamic volume (i.e., their effective size in solution). Following their release from the stationary phase, the acid-terminated polymers also undergo separation according to hydrodynamic volume. Gradient steepness strongly influenced the elution behavior of acid-terminated polymers. Shallow gradients resulted in broader elution profiles reflecting prolonged adsorption-desorption, whereas steeper gradients produced sharper, more symmetrical peaks. The method can be directly coupled to MS, enabling molecular-level characterization of end-group structures and chemical composition across the chromatographic separation. The proposed esSEC-MS method provides a novel strategy for end-group-resolved polymer analysis. Its applicability is demonstrated by monitoring the formation of cyclic structures by intramolecular transesterification and the degradation of an ester-terminated PLGA copolymer over time.
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