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Updated: Jul 19, 2025

Thermal Measurement Techniques in Analytical Microfluidic Devices
Published on: June 3, 2015
Design of enzyme@metal organic framework composites with thermo-responsivity for colourimetric detection of glucose
Muhammad Ali Tajwar1,2, Cheng Cheng1,3, Li Qi1,2
1Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, P.R. China. qili@iccas.ac.cn.
Abstract:
Enzyme immobilization on metal-organic frameworks (MOFs) has interested researchers in recent decades due to the outstanding characteristics of MOFs. However, despite some enzyme@MOF composites exhibiting better tolerance, stability and catalysis than free enzymes, boosting the catalytic performance of stimuli-responsive polymer-grafted MOFs composites remains a challenging task. Herein, a glucose oxidase (GOx)-horseradish peroxidase (HRP)@MOF (UiO-66-NH2, U)@polymer composite with tunable catalytic ability was constructed by modification with thermo-responsive poly(N-isopropylacrylamide) (PN) via a surface-selective post-synthetic protocol. Temperature increases changed the PN-based soft armour from a "stretch" to a "coil" conformation on the MOF surface, resulting in the confinement effect and boosting the catalytic performance of the GOx-HRP@U@PN composites. Compared with its maximum catalytic reaction rate at 25 °C, the proposed composites showed 18-fold improvement in catalytic performance at 37 °C. Additionally, a colourimetric method for serum glucose analysis was developed using a GOx-HRP-based catalytic cascade reaction with a linear range from 0.1 to 2.0 mM and a low detection limit of 0.03 mM. Remarkably, the surface PN-shell-based soft armour proved to be the key factor for enhancing the catalytic performance of the as-designed composites. The co-immobilization of GOx-HRP onto the thermo-responsive U@PN surface provides a new approach for the development of highly sensitive colourimetric glucose sensing protocols.

