Literature DB >> 26259711

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

Xinming Tong1, Soah Lee2, Layla Bararpour3, Fan Yang4.   

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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

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

Mesh:

Substances:

Year:  2015        PMID: 26259711      PMCID: PMC5127624          DOI: 10.1002/mabi.201500245

Source DB:  PubMed          Journal:  Macromol Biosci        ISSN: 1616-5187            Impact factor:   4.979


  48 in total

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Review 7.  PEG hydrogels for the controlled release of biomolecules in regenerative medicine.

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7.  Effects of the poly(ethylene glycol) hydrogel crosslinking mechanism on protein release.

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Review 8.  Vitreous Substitutes as Drug Release Systems.

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