Enzyme immobilization on thermosensitive hydrogel microspheres

Enzyme immobilization on thermosensitive hydrogel microspheres
复制标题

DOI:
10.1016/0927-7765(94)01177-7
复制
发表时间:
1995-06
期刊:
Colloids and Surfaces B: Biointerfaces
影响因子:
--
通讯作者:
T. Shiroya;Nobuko Tamura;Mamoru Yasui;K. Fujimoto;H. Kawaguchi
T. Shiroya;Nobuko Tamura;Mamoru Yasui;K. Fujimoto;H. Kawaguchi
中科院分区:
其他
文献类型:
--
作者:
T. Shiroya;Nobuko Tamura;Mamoru Yasui;K. Fujimoto;H. Kawaguchi

文献摘要

被引文献

相似文献

Precipitation polymerization of N-isopropylacrylamide, acrylamide, and methylenebisacrylamide in water at 70°C resulted in thermosensitive hydrogel microspheres. Carboxyl groups on the microspheres were introduced by hydrolysis, and amino groups by the Hofmann reaction of amide units on the microspheres. Trypsin was immobilized on the carboxylated microspheres using carbodiimide. Phase transitions were detected using a hydrophobic fluorescence probe. The temperatures at which a phase transition occurred were increased by immobilizing enzymes. The enzymatic activity of the immobilized enzymes decreased above the transition temperature. This was attributed to (i) a decrease in the diffusion of substrate; and (ii) entrapment of enzyme in the surface layer of the microspheres. In an attempt to overcome the entrapment, enzymes were immobilized via a hydrophilic spacer (α-(carboxymethyl)-ω-(carboxymethoxy)-poly(oxy-1,2-ethanediyl), PEO acid) to the microspheres. These enzyme-carrying hydrogel microspheres were found to show an enzymatic activity independent of temperature, even though these conjugates show a phase transition at the lower critical solution temperature.