热重分析
纳米孔
Zeta电位
二氧化钛
热稳定性
化学工程
固定化酶
扫描电子显微镜
材料科学
表面改性
生物传感器
傅里叶变换红外光谱
介孔材料
钛
二氧化硅
化学
纳米技术
酶
有机化学
复合材料
催化作用
纳米颗粒
工程类
作者
Lingtian Wu,Shanshan Wu,Zheng Xu,Yibin Qiu,Sha Li,Hong Xu
标识
DOI:10.1016/j.bios.2016.01.045
摘要
ε-Poly-L-lysine (EPL)-modified mesoporous titanium dioxide (M-TiO2) was assembled through the electrostatic attraction between EPL and M-TiO2. Through modification, the M-TiO2 surface tends to form multilayered and complex architectures, which can be used as artificial matrices to change the microenvironment of carriers for enzyme immobilization. The modified M-TiO2 was characterized through scanning electron microscopy, Fourier transform infrared spectroscopy, zeta potential analysis, and thermogravimetric analysis. All of the immobilized enzymes with negative charges display strong storage stability, thermal stability, and good reusability. Results indicate that EPL can self-assemble onto the surface of M-TiO2 and form a considerable number of active coatings. Our results also demonstrate that this simple and novel method can be potentially used to immobilize negatively charged enzymes for biosensor applications.
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