Volume 45, Issue 2 pp. 125-132

Preparation and characterization of α-amylase-immobilized thermal-responsive composite hydrogel membranes

Yi-Ming Sun

Corresponding Author

Yi-Ming Sun

Department of Chemical Engineering, Yuan Ze University, Chung-Li, Taoyuan, Taiwan 320, Republic of China

Department of Chemical Engineering, Yuan Ze University, Chung-Li, Taoyuan, Taiwan 320, Republic of ChinaSearch for more papers by this author
Jyh-Ping Chen

Jyh-Ping Chen

Department of Chemical Engineering, Chang Gung University, Kwei-San, Taoyuan, Taiwan 333, Republic of China

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Ding-Hsin Chu

Ding-Hsin Chu

Department of Chemical Engineering, Yuan Ze University, Chung-Li, Taoyuan, Taiwan 320, Republic of China

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Abstract

Composite hydrogel membranes of crosslinked poly(N-isopropylacrylamide-co-N-acryloxysuccinimide-co-2-hydroxyethyl methacrylate) [P(NIPAAm-NAS-HEMA)] with starch, as a macropore forming agent, on nonwoven polyester was prepared. The membranes could swell and de-swell around the characteristic lower critical solution temperature (LCST) of poly(N-isopropylacrylamide) (PNIPAAm). It was demonstrated that the presence of macropores in the membranes could improve the immobilization efficiency as well as lead to a short responding time upon temperature change across the LCST. Immobilized α-amylase could retain as high as 33% of the activity of the free enzyme with a loading level of 0.60–0.65 mg/cm2 when the membrane preparation and enzyme immobilization conditions were optimized. The half time (T0.5) for the swelling or de-swelling response of the gel phase within the membranes was less than 2 min, and the 90% time (T0.9) was less than 6 min. The permeability for maltose through the membranes could change as much as 4.9-fold when the temperature was raised above or reduced below the LCST. © 1999 John Wiley & Sons, Inc. J Biomed Mater Res, 45, 125–132, 1999.

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