Both condensation beta-cyclodextrin polymer (beta-CDP) and condensatio
n carboxymethylated beta-cyclodextrin polymer (beta-CDPA) were used fo
r preparation of membranes for amperometric glucose biosensors. Glucos
e oxidase (GOD) was covalently immobilized in the membranes and the te
trathiafulvalenium/tetrathiafulvalene (TTF+/TTF) mediating couple was
retained in the beta-CDP membrane due to supramolecular complex format
ion while in the beta-CDPA one due to supramolecular complex formation
as well as ion exchange (by the pending carboxymethyl groups). In the
latter case, retention of the mediator was greatly improved, leading
to a superior biosensor performance. This performance was tested in ph
osphate buffer pH 7.4 with respect to the optimum GOD and TTF loadings
as well as the membrane thickness. Under the optimum conditions, i.e.
, at the 90 units GOD and 0.1 mg TTF loadings and ca. 45 mu m membrane
thickness, the electrode detectability, sensitivity and response time
towards glucose were 0.2 mM, 2.54 mu A ml(-1) and 25.5 s, respectivel
y. The (beta-CDPA)-GOD-TTF biosensor displays excellent selectivity to
wards glucose in the presence of commonly interfering substances, such
as ascorbic acid, uric acid and acetaminophen. The (beta-CDPA)-GOD-TT
F preparation strategy was employed for fabrication of glucose biosens
ors based on a disposable screen-printed Ag-carbon strip two-electrode
transducer.