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. 2018 May 11;8(4):226–233. doi: 10.1016/j.jpha.2018.05.002

Table 2.

Summary of immobilized enzyme microreactors.

Enzyme CE mode Immobilization technique Cartridge temperature (°C) Detection Ref.
Trypsin CZE Glutaraldehyde cross-linking technology 37 UV (214 nm) [58]
Tyrosinase CZE Ionic binding technique with cationic polyelectrolyte hexadimethrine bromide 37 UV (214 nm) [59]
Glucose-6-phosphate dehydrogenase CZE Layer-by-layer electrostatic assembly 22 UV (340 nm) [60]
Cytochrome P450 CZE Magnetic SiMAG-carboxyl microparticles as a support 30 UV (200 nm) [61]
Adenosine deaminase and xanthine oxidase CZE Gold nanoparticles as a support UV (210 nm) [62]
Tyrosinase CZE Glutaraldehyde cross-linking technology 31 UV (214 nm) [64]
Trypsin CZE Based on polydopamine 37 UV (214 nm) [65]
Trypsin CZE Graphene oxide as a support UV (214 nm) [66]
Trypsin CZE Perfusive silica single particles as the frits and large-pore beads as the enzyme supports 22 UV (214, 220 nm) [67]