Fabrication of macroporous hydrogel membranes using photolithography for enzyme immobilization

Dongkil Choi, Woojin Lee, Yeol Lee, Dae Nyun Kim, Jin Won Park, Won-Gun Koh

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Background: The main problem when immobilizing enzyme inside hydrogel is the activity loss of the trapped enzymes due to the limitation on diffusion. In this study, macroporous poly(ethylene glycol) (PEG) hydrogel membrane was fabricated using photolithography to enhance the activity of immobilized enzyme. Result: Photopolymerization through the designed photomask produced crosslinked hydrogel with tunnel-like macropores which were completely opened from top to bottom of the hydrogel membranes. Arrays of pores with 50 μm and 100 μm diameters were successfully created in the hydrogel membranes, and the pore density could be controlled by changing the photomask design. An activity study demonstrated that there was an enhancement of more than 50% in glucose oxidase activity in the macroporous membrane in comparison to the nonporous membrane. The activity of immobilized enzyme could be further enhanced by increasing the pore density of the hydrogel membranes or by using a higher molecular weight PEG. Conclusion: Increased enzymatic activity was observed in macroporous hydrogel membranes compared with nonporous hydrogel membranes due to the higher surface to volume ratio provided by the macroporous structure. Compared with other methods of obtaining porous hydrogel, the proposed method is much simpler and can minimize the deactivation of enzyme.

Original languageEnglish
Pages (from-to)252-259
Number of pages8
JournalJournal of Chemical Technology and Biotechnology
Volume83
Issue number3
DOIs
Publication statusPublished - 2008 Mar 1

Fingerprint

Enzyme immobilization
Hydrogel
Photolithography
Hydrogels
Immobilization
immobilization
enzyme
membrane
Membranes
Fabrication
Enzymes
Polyethylene glycols
Photomasks
Immobilized Enzymes
Glucose Oxidase
macropore
Glucose oxidase
Ethylene Glycol
Photopolymerization
ethylene

All Science Journal Classification (ASJC) codes

  • Biotechnology
  • Chemical Engineering(all)
  • Renewable Energy, Sustainability and the Environment
  • Fuel Technology
  • Waste Management and Disposal
  • Pollution
  • Organic Chemistry
  • Inorganic Chemistry

Cite this

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abstract = "Background: The main problem when immobilizing enzyme inside hydrogel is the activity loss of the trapped enzymes due to the limitation on diffusion. In this study, macroporous poly(ethylene glycol) (PEG) hydrogel membrane was fabricated using photolithography to enhance the activity of immobilized enzyme. Result: Photopolymerization through the designed photomask produced crosslinked hydrogel with tunnel-like macropores which were completely opened from top to bottom of the hydrogel membranes. Arrays of pores with 50 μm and 100 μm diameters were successfully created in the hydrogel membranes, and the pore density could be controlled by changing the photomask design. An activity study demonstrated that there was an enhancement of more than 50{\%} in glucose oxidase activity in the macroporous membrane in comparison to the nonporous membrane. The activity of immobilized enzyme could be further enhanced by increasing the pore density of the hydrogel membranes or by using a higher molecular weight PEG. Conclusion: Increased enzymatic activity was observed in macroporous hydrogel membranes compared with nonporous hydrogel membranes due to the higher surface to volume ratio provided by the macroporous structure. Compared with other methods of obtaining porous hydrogel, the proposed method is much simpler and can minimize the deactivation of enzyme.",
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Fabrication of macroporous hydrogel membranes using photolithography for enzyme immobilization. / Choi, Dongkil; Lee, Woojin; Lee, Yeol; Kim, Dae Nyun; Park, Jin Won; Koh, Won-Gun.

In: Journal of Chemical Technology and Biotechnology, Vol. 83, No. 3, 01.03.2008, p. 252-259.

Research output: Contribution to journalArticle

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AU - Kim, Dae Nyun

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AU - Koh, Won-Gun

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N2 - Background: The main problem when immobilizing enzyme inside hydrogel is the activity loss of the trapped enzymes due to the limitation on diffusion. In this study, macroporous poly(ethylene glycol) (PEG) hydrogel membrane was fabricated using photolithography to enhance the activity of immobilized enzyme. Result: Photopolymerization through the designed photomask produced crosslinked hydrogel with tunnel-like macropores which were completely opened from top to bottom of the hydrogel membranes. Arrays of pores with 50 μm and 100 μm diameters were successfully created in the hydrogel membranes, and the pore density could be controlled by changing the photomask design. An activity study demonstrated that there was an enhancement of more than 50% in glucose oxidase activity in the macroporous membrane in comparison to the nonporous membrane. The activity of immobilized enzyme could be further enhanced by increasing the pore density of the hydrogel membranes or by using a higher molecular weight PEG. Conclusion: Increased enzymatic activity was observed in macroporous hydrogel membranes compared with nonporous hydrogel membranes due to the higher surface to volume ratio provided by the macroporous structure. Compared with other methods of obtaining porous hydrogel, the proposed method is much simpler and can minimize the deactivation of enzyme.

AB - Background: The main problem when immobilizing enzyme inside hydrogel is the activity loss of the trapped enzymes due to the limitation on diffusion. In this study, macroporous poly(ethylene glycol) (PEG) hydrogel membrane was fabricated using photolithography to enhance the activity of immobilized enzyme. Result: Photopolymerization through the designed photomask produced crosslinked hydrogel with tunnel-like macropores which were completely opened from top to bottom of the hydrogel membranes. Arrays of pores with 50 μm and 100 μm diameters were successfully created in the hydrogel membranes, and the pore density could be controlled by changing the photomask design. An activity study demonstrated that there was an enhancement of more than 50% in glucose oxidase activity in the macroporous membrane in comparison to the nonporous membrane. The activity of immobilized enzyme could be further enhanced by increasing the pore density of the hydrogel membranes or by using a higher molecular weight PEG. Conclusion: Increased enzymatic activity was observed in macroporous hydrogel membranes compared with nonporous hydrogel membranes due to the higher surface to volume ratio provided by the macroporous structure. Compared with other methods of obtaining porous hydrogel, the proposed method is much simpler and can minimize the deactivation of enzyme.

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