Publication | Closed Access
Covalent Immobilization of Glucose Oxidase on Well-Defined Poly(glycidyl methacrylate)−Si(111) Hybrids from Surface-Initiated Atom-Transfer Radical Polymerization
195
Citations
62
References
2005
Year
EngineeringSmart PolymerChemistryEnzyme ImmobilizationWell-defined PolyPolymersChemical EngineeringSilicon SurfaceSingle-crystal Silicon SurfacePolymer ChemistryMolecular EngineeringBiomolecular EngineeringFree EnzymeSurface FunctionalizationPolymer ScienceGlucose OxidaseCovalent ImmobilizationImmobilized EnzymePolymerization KineticsPolymer ReactionPolymer Synthesis
A simple one-step procedure was employed for the covalent immobilization of an atom-transfer radical polymerization (ATRP) initiator, via the robust Si-C bond, on the hydrogen-terminated Si(111) surface (Si-H surface). Well-defined poly(glycidyl methacrylate) [P(GMA)] brushes, tethered directly on the (111)-oriented single-crystal silicon surface, were prepared via surface-initiated ATRP. Kinetics study on the surface-initiated ATRP of glycidyl methacrylate revealed that the chain growth from the silicon surface was consistent with a "controlled" process. A relatively high concentration of glucose oxidase (GOD; above 0.2 mg/cm2) could be coupled directly to the well-defined P(GMA) brushes via the ring-opening reaction of the epoxide groups with the amine moieties of the enzyme. The resultant GOD-functionalized P(GMA) brushes, with the accompanying hydroxyl groups from the ring-opening reaction of the epoxide groups, serves as an effective spacer to provide the GOD with a higher degree of conformational freedom and a more hydrophilic environment. An equivalent enzyme activity above 1.6 units/cm2 [micromoles of beta-D-(+)-glucose oxidized to d-gluconolactone per minute per square centimeter] and a corresponding relative activity of about 60% could be readily achieved. The immobilized GOD also exhibited an improved stability during storage over that of the free enzyme. The GOD-functionalized silicon substrates are potentially useful to the development of silicon-based glucose biosensors.
| Year | Citations | |
|---|---|---|
Page 1
Page 1