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] |