Cited by 348biodegradable polymer synthesis and propertiesAdvanced Polymer Synthesis and CharacterizationPolymer Surface Interaction Studies

On the biodegradability of polyethylene glycol, polypeptoids and poly(2-oxazoline)s

Ulbricht, Juliane, Jordan, Rainer, Luxenhofer, Robert·2014·Biomaterials

Abstract

Despite being the gold standard of hydrophilic biomaterials and well known sensitivity of polyethylene glycol (PEG) against oxidative degradation, very little information on the decomposition of PEG under biological oxidative stress can be found in the literature. Poly(2-oxazoline)s (POx) and polypeptoids (POI), two pseudo-polypeptides, have attracted some attention for the use as biomaterials and alternative to PEG with an altered stability against oxidative degradation. All three polymer families are supposedly non-biodegradable, which could be seen as one of their main disadvantages. Here, we present evidence that PEG, POx and POI are degradable by oxidative degradation under biologically relevant conditions. Transition metal catalysed generation of reactive oxygen species (ROS) leads to a pronounced time and concentration dependent degradation of all polymers investigated. While we do not envision oxidative degradation to be of relevance in the short-term usage of these polymers, mid- and long-term biodegradability in vivo appears feasible. Moreover, influence in ROS mediated signalling cascades may be one mechanism how synthetic polymers influence complex cellular processes.

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Crossref · 10.1016/j.biomaterials.2014.02.029

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  • Oxidative degradation driven by reactive oxygen species in inflamed tissues can compromise PEG's long-term stability in vivo and reduce its effectiveness in maintaining prolonged tissue separation.

    “In particular, oxidative degradation—driven by reactive oxygen species (ROS) in inflamed tissues—can compromise PEG’s long-term stability in vivo, reducing its effectiveness in maintaining prolonged tissue separation [219].”

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Authors
Ulbricht, J., Jordan, R., & Luxenhofer, R.
Affiliations
  • University of Würzburg (DE)
  • Technische Universität Dresden (DE)
Venue
Biomaterials
Publisher
Elsevier BV
Published
2014-06
Volume
35
Issue
17
Pages
4848-4861
ISSN
0142-9612 (ISSN-L)
OpenAlex
W2147063650
Cited by
348
References
8
Citations by year
2026: 20 · 2025: 22 · 2024: 24 · 2023: 35 · 2022: 33 · 2021: 29 · 2020: 46 · 2019: 29 · 2018: 23 · 2017: 23 · 2016: 30 · 2015: 26 · 2014: 8
FWCI
10.30
Type
journal article
Language
en
Open access
closed
Locations
  • Biomaterials (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Fonds der Chemischen Industrie
  • State of Bavaria
  • German Plastics Center SKZ
  • Julius-Maximilians Universität Würzburg
Topics
  • Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
  • Physical Sciences › Chemistry › Organic Chemistry › Advanced Polymer Synthesis and Characterization
  • Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
Keywords
polyethylene glycol, polypeptoids, poly(2-oxazoline), oxidative degradation, biodegradability, reactive oxygen species, transition metal catalysis
MeSH terms
Biocompatible Materials, Hydrogen Peroxide, Oxazoles, Oxidation-Reduction, Peptides, Polyethylene Glycols, Reactive Oxygen Species, Peptoids

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