LONG-FUNCTIONING BETA-D-GLUCOSE AND L-LAC TATE BIOSENSORS FOR CONTINUOUS FLOW-THROUGH MEASUREMENTS FOR FOULING-RESISTANT AND SELECTIVITY-OPTIMIZED SERUM-ANALYSIS AND HAEMOANALYSIS
Jg. Schindler et al., LONG-FUNCTIONING BETA-D-GLUCOSE AND L-LAC TATE BIOSENSORS FOR CONTINUOUS FLOW-THROUGH MEASUREMENTS FOR FOULING-RESISTANT AND SELECTIVITY-OPTIMIZED SERUM-ANALYSIS AND HAEMOANALYSIS, European journal of clinical chemistry and clinical biochemistry, 32(8), 1994, pp. 599-608
Bioelectrochemical membrane-electrodes for O-2-sensitive enzymatic flo
w-through analysis of beta-D-glucose and L-lactate are described. The
enzyme-membranes of the biosensors consist of glucose-oxidase or lacta
te-oxidase molecules cross-linked with glutardialdehyde between two di
alysis membranes. The accuracy of the biosensors is demonstrated by el
ectroanalysis of diluted control serum and compared with redox-mediato
r-free H2O2 detection and photometric methods. Continuous haemoanalysi
s of uncoagulated blood was carried out, using an intermediate carrier
stream with additive systems. Tangential streaming to the miniaturize
d dialysis chamber with a circular channel minimizes blockage of the p
ores of the dialysis membrane by erythrocytes, leukocytes or protein.
An oxygenator pump for the exchange of gases between the buffered solu
tion of the intermediate carrier and the surrounding atmosphere guaran
tees a constant oxygen partial pressure within the carrier stream. The
pulsations produced by the oxygenator pump are dampened by a miniatur
e pressure balance chamber with an unsignificant dead space volume for
protecting the enzyme membrane of the sensor. Glutardialdehyde inhibi
ts growth of microorganisms and any resulting oxygen consumption, so t
hat even in protein-containing measuring solutions enzyme electrodes c
an be used without interference from microbial contamination. The bioe
lectrochemical measuring system can therefore also be employed for the
electroanalysis of fermentation solutions. For continuous flow-throug
h measurements, it is necessary to change the glucose-oxidase membrane
s after 100-150 days, and the lactate-oxidase membranes after 3-6 week
s.