Why degradable polymers undergo surface erosion or bulk erosion
Abstract
A theoretical model was developed that allows to predict the erosion mechanism of water insoluble biodegradable polymer matrices. The model shows that all degradable polymers can undergo surface erosion or bulk erosion. Which way a polymer matrix erodes after all depends on the diffusivity of water inside the matrix, the degradation rate of the polymer's functional groups and the matrix dimensions. From these parameters the model allows to calculate for an individual polymer matrix a dimensionless 'erosion number' epsilon. The value of epsilon indicates the mode of erosion. Based on epsilon, a critical device dimension Lcritical can be calculated. If a matrix is larger than Lcritical it will undergo surface erosion, if not it will be bulk eroding. Lcritical values for polymers were estimated based on literature data. Polyanhydrides were found to be surface eroding down to a size of approximately Lcritical = 10(-4) m while poly(alpha-hydroxy esters) matrices need to be larger than Lcritical = 10(-1) m to lose their bulk erosion properties. To support our theoretical findings it was shown experimentally that poly(alpha-hydroxy ester) matrices, which are considered classical bulk eroding materials, can also undergo surface erosion.
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PCL degrades by surface erosion in an alkaline environment with high pH.
“However, the degradation mechanism of PCL in the alkaline environment with high pH is surface erosion.”
From A strategy to tailor the mechanical and degradation properties of PCL-PEG-PCL based copolymers for biomedical application (2023) · cites this paper as [47]
In alkaline high pH, mass loss appears in the initial stage and degradation rate is linear.
“Under these conditions, the mass loss appears in the initial stage and the degradation rate are linear [46,47].”
From A strategy to tailor the mechanical and degradation properties of PCL-PEG-PCL based copolymers for biomedical application (2023) · cites this paper as [47]
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“Under these conditions, the mass loss appears in the initial stage and the degradation rate are linear [46,47].”
Background
- Authors
- Burkersroda, F. V., Schedl, L., & Göpferich, A.
- Affiliations
- University of Regensburg (DE)
- Friedrich-Alexander-Universität Erlangen-Nürnberg (DE)
- Corresponding author
- Göpferich, Achim
- ORCID
- Göpferich, Achim
- Venue
- Biomaterials
- Publisher
- Elsevier BV
- Published
- 2002-11
- Volume
- 23
- Issue
- 21
- Pages
- 4221-4231
- ISSN
- 0142-9612 (ISSN-L)
- OpenAlex
- W1992801092
- Cited by
- 1,146
- References
- 0
- Citations by year
- 2026: 59 · 2025: 63 · 2024: 65 · 2023: 65 · 2022: 73 · 2021: 66 · 2020: 68 · 2019: 69 · 2018: 56 · 2017: 41 · 2016: 61 · 2015: 42 · 2014: 59 · 2013: 58 · 2012: 54
- FWCI
- 9.64
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biomaterials (publishedVersion)
- PubMed (publishedVersion)
- University of Regensburg Publication Server (University of Regensburg) (acceptedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (GO 565/3-2)
- Topics
- Physical Sciences › Materials Science › Biomaterials › biodegradable polymer synthesis and properties
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Medicine › Hydrogels: synthesis, properties, applications
- Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmaceutical Science › Advanced Drug Delivery Systems
- Keywords
- biodegradable polymers, surface erosion, bulk erosion, water diffusion coefficient, polyanhydrides
- MeSH terms
- Polylactic Acid-Polyglycolic Acid Copolymer, Biocompatible Materials, Hydrogen-Ion Concentration, Materials Testing, Mathematics, Microscopy, Electron, Scanning, Models, Theoretical, Polyesters, Polyglycolic Acid, Polymers, Water, Lactic Acid, Prostheses and Implants
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