We adapted a new technology for the modification of carbon base electr
odes for use as probe-type, potentially-implantable glucose sensors. C
arbon rods (diameter 0.3 mm) were modified by repeated potential cycli
ng in 0.1 M potassium hexacyanoferrate (III). The modified-carbon elec
trodes were sealed in plastic pipette tips with an exposed reaction ar
ea where glucose oxidase was immobilized using glutaraldehyde. An oute
r membrane of Nafion, followed by 15% (w/v) polyurethane, was applied
over the enzyme layer. The miniature modified-carbon glucose sensors d
isplayed a sensitivity to glucose in phosphate-buffered saline of 91.4
+/-19 nA/mM (mean+/-SEM) and a linear range up to 5.3+/-1 mM glucose w
hen operated at 750 mV versus a silver/silver chloride reference. Corr
esponding, unmodified-carbon based glucose sensors displayed a lower s
ensitivity of 20.7+/-3 nA/mM with a linear range up to 3.8+/-0.5 mM. T
he modified-carbon glucose sensors responded to glucose when operated
in plasma but with a reduced sensitivity compared with that in buffere
d saline. Glucose sensors displayed good stability for up to 6.5 days
during continuous operation in 5 mM buffered glucose solution. Interfe
rence from ascorbate and 4-acetamidophenol at both physiological and p
harmacological ranges was significantly lower at the modified-carbon b
ase electrodes than that at the unmodified-carbon base electrodes. Als
o, the relatively large effect of ascorbate and 4-acetamidophenol at t
he unmodified-carbon base electrode was reduced considerably when the
base electrode was coated with glucose oxidase, Nafion and polyurethan
e membranes. (C) 1996 Elsevier Science Limited