Immobilization Protocols of Nanozyme with Different Morphologies in Microfluidic Chips for Biosensing
Caixia Zhu1,2, Kaiyuan Wang1, Yanqin Lv3
1Jiangsu Engineering Research Center of Smart Carbon-Rich Materials and Devices, Jiangsu Province Hi-Tech Key Laboratory for Bio-Medical Research, School of Chemistry and Chemical Engineering, Medical School, Southeast University, Nanjing 21189, China.
Optimizing nanozyme immobilization on microfluidic chips (MFCs) is key for catalysis. Elongated nanozyme structures (1D/2D) offer better active site exposure than 0D ones, enhancing biosensor performance.
Area of Science:
- * Nanotechnology and Materials Science
- * Chemical Engineering and Microfluidics
- * Analytical Chemistry and Biosensing
Background:
- * Microfluidic chips (MFCs) are efficient platforms for nanozyme-based cascade catalysis and continuous detection.
- * Immobilization strategies critically impact nanozyme catalytic performance by balancing activity and stability.
- * Nanozyme morphology influences immobilization efficiency and active site accessibility.
Purpose of the Study:
- * To propose tailored immobilization strategies for nanozymes with diverse morphologies (0D, 1D, 2D) in MFCs.
- * To investigate the relationship between nanozyme morphology, immobilization, and catalytic efficiency.
- * To develop an optimized microfluidic biosensor for enhanced dopamine detection.
Main Methods:
- * Synthesis and characterization of cobalt-doped carbon nanozymes with 0D, 1D, and 2D morphologies.
- * Immobilization of nanozymes within MFC channels, exploring different strategies.
- * Mechanistic studies to understand nanozyme-channel wall interactions and active site blockage.
- * Development and testing of a microfluidic biosensor for dopamine detection.
Main Results:
- * Immobilization primarily occurs via physical contact with MFC channel walls, potentially blocking active sites.
- * 1D and 2D nanozymes, with their extended structures, showed better immobilization and active site exposure than 0D nanozymes.
- * Binder incorporation was crucial for 0D nanozymes to prevent deep embedding and maximize surface exposure.
- * Optimized immobilization interfaces led to a microfluidic biosensor with enhanced stability and sensitivity for dopamine detection.
Conclusions:
- * Nanozyme morphology significantly affects immobilization outcomes and catalytic performance in MFCs.
- * Tailored immobilization strategies, considering morphology and binders, are essential for maximizing nanozyme efficiency.
- * This study provides a framework for designing practical nanozyme-modified MFC systems for various applications.
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