葡萄糖氧化酶
生物传感器
介孔材料
化学
介孔二氧化硅
吸附
固定化酶
戊二醛
化学工程
小泡
纳米技术
介孔有机硅
共价键
色谱法
有机化学
催化作用
材料科学
酶
生物化学
膜
工程类
作者
Guowei Zhou,Ka Kei Fung,Ling Wai Wong,Yijian Chen,Reinhard Renneberg,Shihe Yang
出处
期刊:Talanta
[Elsevier BV]
日期:2011-05-01
卷期号:84 (3): 659-665
被引量:41
标识
DOI:10.1016/j.talanta.2011.01.058
摘要
The use of rod-like and vesicle-like mesoporous SiO(2) particles for fabricating high performance glucose biosensors is reported. The distinctively high surface areas of mesoporous structures of SiO(2) rendered the adsorption of glucose oxidase (GOx) feasible. Both morphologies of SiO(2) enhanced the sensitivities of glucose biosensors, but by a factor of 36 for vesicle-like SiO(2) and 18 for rod-like SiO(2), respectively. The greater enhancement of vesicle-like SiO(2) can be accounted for by its higher specific surface area (509 m(2)g(-1)) and larger total pore volume (1.49 cm(3)g(-1)). Interestingly, the current responses of GOx immobilized in interior channels of the mesoporous SiO(2) were enhanced much more than those of simple mixtures of GOx and the mesoporous SiO(2). This suggests that the enhancement of current responses arise not only from the high surface area of SiO(2) for high enzyme loading, but also from the improved enzyme activity upon its adsorption on mesoporous SiO(2). Also compared were the performances of glucose biosensors with GOx immobilized on mesoporous SiO(2) by physical adsorption and by covalent binding to 3-aminopropyltrimethoxysilane (APTMS) modified SiO(2) using glutaraldehyde as the cross-linker. The covalent binding approach resulted in higher enzyme loading but lower current sensitivity than with the physical adsorption.
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