Search PubMed⌕ Search

Biomedical subjects

G de Oliveira Neto

Publications and source records attributed to G de Oliveira Neto.

3 recordsLinked to original sources

Study of NADH stability using ultraviolet-visible spectrophotometric analysis and factorial design.

The chemical stability of nicotinamide adenine dinucleotide coenzyme (NADH/NAD+) and its derivatives (NADPH/NADP+) was investigated using changes in the UV-visible absorption spectra of these compounds. The spectra of cofactor (reduced form) were monitored at 340 nm wavelength in different buffers, showing a faster degradation in phosphate buffer. This was assigned to the adduct formation between phosphate and NADH (pyridine ring). The three-factor-two-level factorial design study evaluated the contributions: buffers (phosphate and Pipes 0.1 M), pH's (6.8 and 7.8), and temperature (25 and 30 degrees C). The freshly prepared aqueous solutions of coenzyme were analyzed after 40 min under the different conditions (eight assays in triplicate) of the experiment. The main observed effects of the NADH oxidation were, in increasing order, pH, temperature, and buffer without appreciable interactive effects. Therefore, it was verified that the better conditions for cofactor use were alkaline media employing Pipes buffer or its derivatives and low temperatures.

Buffers↗

Bombardier beetle based biosensor.

A biosensor constructed by combining an oxygen electrode with the liquid ejected by bombardier beetles (Pheropsophus aequinoctialis) immobolized on a collagen membrane is developed for hydrogen peroxide. The sensor presents a linear range of 2.0 x 10(-4)-2.0 x 10(-3) M and a reproductibility of approximately 2%. It shows a better lifetime than similar ones employing purified catalase. The selectivity is good since other enzymes are not present in the natural source employed.

Animals↗

Determination of urea in serum by using naturally immobilized urease in a flow injection conductimetric system.

A flow injection method was developed, aimed at the determination of urea in human serum. The system makes use of the naturally immobilized urease present in Canavalia ensiformis DC (jack bean). A column is filled with small pieces of this bean, and the sample (50 microliters) containing urea passes through it carried by a 1% NaCl solution. On leaving the column the stream is merged with an alkaline reagent (0.5 mol dm-3 NaOH; 0.5% disodium dihydrogen ethylenediaminetetraacetate). The ammonium ions, arising from the enzymatic reaction that occurs inside the column, are changed into the molecular form, which permeates a polytetrafluoroethylene membrane and is received in a de-ionized water acceptor stream. The ammonia ionizes causing an increase in the conductance, which is proportional to the urea content of the sample. About 40 samples can be processed in 1 h with negligible carry-over and with a relative standard deviation of 1% or less. The results are in agreement with those obtained by a standard spectrophotometric method.

Conductometry↗