Preparation of interpenetrating polymer network composed of poly(ethylene glycol) and poly(acrylamide) hydrogels as a support of enzyme immobilization
Autor: | Jinwon Park, Woojin Lee, Dongkil Choi, Dae Nyun Kim, Won Gun Koh, Yeol Lim Lee |
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Rok vydání: | 2008 |
Předmět: |
Materials science
Polymers and Plastics biology Immobilized enzyme technology industry and agriculture macromolecular substances complex mixtures Enzyme assay chemistry.chemical_compound chemistry Chemical engineering Acrylamide PEG ratio Polymer chemistry Self-healing hydrogels biology.protein Glucose oxidase Interpenetrating polymer network Ethylene glycol |
Zdroj: | Polymers for Advanced Technologies. 19:852-858 |
ISSN: | 1099-1581 1042-7147 |
DOI: | 10.1002/pat.1047 |
Popis: | Poly(ethylene glycol)(PEG)-based interpenetrating polymeric network (IPN) hydrogels were prepared for the application of enzyme immobilization. Poly(acrylamide)(PAAm) was chosen as the other network of IPN hydrogel and different concentration of PAAm networks were incorporated inside the PEG hydrogel to improve the mechanical strength and provide functional groups that covalently bind the enzyme. Formation of IPN hydrogels was confirmed by observing the weight per cent gain of hydrogel after incorporation of PAAm network and by attenuated total reflectance/Fourier transform infrared (ATR/FTIR) analysis. Synthesis of IPN hydrogels with higher PAAm content produced more crosslinked hydrogels with lower water content (WC), smaller Mc and mesh size, which resulted in enhanced mechanical properties compared to the PEG hydrogel. The IPN hydrogels exhibited tensile strength between 0.2 and 1.2 MPa while retaining high levels of hydration (70–81% water). For enzyme immobilization, glucose oxidase (GOX) was immobilized to PEG and IPN hydrogel beads. Enzyme activity studies revealed that although all the hydrogels initially had similar enzymatic activity, enzyme-immobilizing PEG hydrogels lost most of the enzymatic activity within 2 days due to enzyme leaching while IPN hydrogels maintained a maximum 80% of the initial enzymatic activity over a week due to the covalent linkage between the enzyme and amine groups of PAAm. Copyright © 2008 John Wiley & Sons, Ltd. |
Databáze: | OpenAIRE |
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