Glucose oxidase method for continuous automated blood glucose determination.

A glucoseoxidase-peroxidasemethod for continuous automated monitoring of blood glucosehas been developed.The responseis linear over the range 0-800 mg/100 ml. Sensitivity can be maintained for 24 hr or longer and can be restored by rinsing the analytic system with sulfuric acid to permit studies of longer than 48 hr in duration. A precisionof ± 1% can be maintained between rinsesfor samplescontaining 100600 mg of glucoseper 100 ml. This method is satisfactorily specific for glucose: The response with other sugars is less than 1% of the response obtained with the same concentration of glucose. Ascorbic acid causes no significant inhibition of the response to glucose. The inhibition by uric acid has been reduced fifty-fold compared to that in other methods. Transit through the sampling catheter and analytic system requires 15 mm. Timed from the first detectable response to a change in concentration, 25% of total responseis achieved in 30 sec and 90% in 80 sec. Fifty percent of an oscillation with a half-period of 45 sec can be detected; no oscillations this short were observedin records of human blood glucose. Applicability and feasibility of this method have been demonstrated in over 2000 hr of repeated blood glucose recordingsin 12 diabetic and 6 normal subjects.