Preparation of poly(ethylene glycol) hydrogels with different network structures for the application of enzyme immobilization

Dongkil Choi, Woojin Lee, Jinwon Park, Wongun Koh

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

In this study, poly(ethylene glycol) (PEG)-based hydrogels having different network structures were synthesized by UV-initiated photopolymerization and used for the enzyme immobilization. PEGs with different molecular weight were acrylated by derivatizing both ends with acryloyl chloride and photopolymerization of PEG-diacrylate (PEG-DA) yielded crosslinked hydrogel network within 5 seconds. Attachment of acrylate groups and gelation were confirmed by ATR/FT-IR and FT-Raman spectroscopy. Network structures of hydrogels could be easily controlled by changing the molecular weight (MW) of PEG-DA and characterized by calculating molecular weight between crosslinks and mesh size from the swelling measurement. Synthesis of hydrogels with higher MW of PEG produced less crosslinked hydrogels having higher water content, larger value of Mc and mesh size, which resulted in enhanced mass transfer but loss of mechanical properties. For the enzyme immobilization, glucose oxidase (GOX) was immobilized inside PEG hydrogels by means of physical entrapment and covalent immobilization. Encapsulated GOX were covalently bound to PEG backbone using acryloyl-PEG-N-hydroxysuccinimide and maintained their activity over a week period without leakage. Kinetic study indicated that immobilized enzyme inside hydrogel prepared from higher MW of PEG possessed lower apparent Km (Michaelis-Menten constant) and higher activity.

Original languageEnglish
Pages (from-to)345-356
Number of pages12
JournalBio-Medical Materials and Engineering
Volume18
Issue number6
DOIs
Publication statusPublished - 2008

All Science Journal Classification (ASJC) codes

  • Biomaterials
  • Biomedical Engineering

Fingerprint Dive into the research topics of 'Preparation of poly(ethylene glycol) hydrogels with different network structures for the application of enzyme immobilization'. Together they form a unique fingerprint.

  • Cite this