Influence of gamma irradiation on a natural source of peroxidase and its effect in the reagentless amperometric biosensor for hydrogen peroxide.

Peroxidase was extracted from a natural source (turnip) and irradiated with 60Co (0.1 kGy). It was then used in the construction of biosensors for hydrogen peroxide determination, in order to study the effect of the gamma irradiation on the performance of the biosensors. The biosensors were constructed using two immobilization procedures: cross-linking with glutaraldehyde and covalent binding through carbodiimide. The biosensor prepared using covalent binding through carbodiimide showed a higher sensitivity for H2O2. A good enhancement in stability and sensitivity was obtained for the biosensors from irradiated material, when compared to biosensors prepared with non-irradiated enzyme. However, the initial linear response range (1.0 to 10.0 mmol dm-3) and response time (0.5 s) were equal with or without irradiation.

Development of a tubular periodate electrode for flow-injection determination of glycerol.

Periodate electrodes without inner reference solution based on tetraoctylammonium periodate plus solvent mediator (dibutyl phthalate or 2-nitrophenyl octylether) were constructed. Linear dynamic range, practical detection limit, slope, stability, selectivity coefficients, pH dependence, response time and lifetime were evaluated. A tubular version was further developed and coupled to a flow-injection system for glycerol determination in samples relevant to the industrial production of soaps, detergents and similar. The method involves glycerol oxidation by periodate with potentiometric evaluation of its consumption. The influence of oxidizing agent concentration (10(-5)-10(-2)M NalO(4)), ionic strength (0.0-1.0M Na(2)SO(4)) and mean resident time were investigated and the feasibility of using a single-fine manifold was discussed. The proposed system handles about 40 samples/hr, is very stable and suitable to industrial control. Results within the 1000 and 5000 mg/l range glycerol are precise (r.s.d. <0.005) and in fair agreement with conventional procedures. Baseline drift or noise is not observed and a thermostat water bath is not required. A noteworthy feature is the almost linear relationship between glycerol concentration and recorded peak height which is a consequence of combined effects of reaction kinetics and electrode Nernstian response.