J. Jezkova et al., STABILIZATION OF AN OSMIUM BIS-BIPYRIDYL POLYMER-MODIFIED CARBON-PASTE AMPEROMETRIC GLUCOSE BIOSENSOR USING POLYETHYLENEIMINE, Electroanalysis, 9(13), 1997, pp. 978-984
The modification of carbon paste electrodes by incorporation of the en
zyme glucose oxidase (GOx) and a conducting redox osmium bis-bipyridyl
poly(4-vinylpyridine) polymer (Os-polymer) is described. The resultin
g enzyme electrodes were operated as amperometric glucose sensors in t
he presence or absence of a stabilizer, polyethyleneimine (PEI), mixed
into the paste. Cyclic voltammetric studies showed that Os-polymer co
ntaining Os2+/3+ redox couple mediated the electron transfer from redu
ced GOx to the carbon paste electrode material. Steady-state amperomet
ric responses of the sensors to 2-120 mM glucose at an operating poten
tial of 350 mV (vs. Ag/AgCl) were determined in 0.1 M phosphate buffer
(pH 7.0) medium. The study showed that PEL enhances both. the sensiti
vity and stability of the carbon paste enzyme electrode and that a dif
fusion-limited step precedes electrocatalytic reactions of the biosens
or. Cyclic voltammetric data and the Arrhenius analysis of the apparen
t turnover rate constant, k(cat)', showed that PET decreases the diffu
sion limitations of CPE, thereby increasing the frequency of collision
of reacting species in this biosensor format.