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Macromol Biosci. 2015 Dec;15(12):1679-86. doi: 10.1002/mabi.201500245. Epub 2015 Aug 11.

Long-Term Controlled Protein Release from Poly(Ethylene Glycol) Hydrogels by Modulating Mesh Size and Degradation.

Author information

1
Department of Orthopaedic Surgery, Stanford University, CA, 94305, USA.
2
Department of Materials Science and Engineering, Stanford University, CA, 94305, USA.
3
Department of Bioengineering, Stanford University, CA, 94305, USA.
4
Departments of Orthopaedic Surgery and Bioengineering, Stanford University, CA, 94305, USA. fanyang@stanford.edu.

Abstract

Poly(ethylene glycol) (PEG)-based hydrogels are popular biomaterials for protein delivery to guide desirable cellular fates and tissue repair. However, long-term protein release from PEG-based hydrogels remains challenging. Here, we report a PEG-based hydrogel platform for long term protein release, which allows efficient loading of proteins via physical entrapment. Tuning hydrogel degradation led to increase in hydrogel mesh size and gradual release of protein over 60 days of with retained bioactivity. Importantly, this platform does not require the chemical modification of loaded proteins, and may serve as a versatile tool for long-term delivery of a wide range of proteins for drug-delivery and tissue-engineering applications.

KEYWORDS:

controlled protein release; degradation; hydrogels; mesh size; poly(ethylene glycol)

PMID:
26259711
PMCID:
PMC5127624
DOI:
10.1002/mabi.201500245
[Indexed for MEDLINE]
Free PMC Article

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