Sueli Pércio Quináia

Composição química e atividade biológica de extrato oleoso de própolis: uma alternativa ao extrato etanólico

Propolis is mostly used as hydroalcoholic extract. Recently there has been a growing number of patents dealing with new solvents for preparing propolis extracts. This study aimed to prepare edible oil propolis extracts and compare their chemical composition and biological activity with ethanolic propolis extracts. ESI-MS and spectrophotometric methods were used for qualitative and quantitative analyses, respectively. Antibacterial activity was evaluated by diffusion in agar. Cytotoxicity was tested by MTT assay using tumor cell lines. The oil is able to extract bioactive compounds from propolis. Further studies are needed to improve extraction efficiency and to characterize the active components.

Direct determination of Cd, Pb and Cr in honey by slurry sampling electrothermal atomic absorption spectrometry

Slurry sampling electrothermal atomic absorption spectrometry was used for direct determination of Cr, Pb and Cd in honey without sample pretreatment. The honey slurries were prepared in aqueous solution containing hydrogen peroxide and nitric acid. The slurries were directly introduced in the pyrolytic graphite tubes. Pd-Mg was used as a chemical modifier only for Cd determination. Analytical curves were performed with aqueous standards for Pb and Cr and with addition of fructose for Cd. The quantification limits for Cd, Pb and Cr were 2.0, 5.4 and 9.4ngg(-1), respectively. Acceptable precision of the methodology was obtained through repeatability and intermediate precision. In the accuracy study, recoveries were satisfactory (94-101%) for the three elements. The methodology was applied in honey from Paraná (Brazil). The concentrations of Pb, Cd and Cr ranged from 141 to 228ngg(-1), <2.0 to 8ngg(-1) and 83 to 94ngg(-1), respectively.

Avaliação da contaminação de metais em sedimentos superficiais das praias do lago de Itaipu

This work was performed to evaluate the distribution of metals Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb and Zn in the sediment surface in the Itaipu Lake-PR-Brazil. It was also performed to measurement the pH, phosphorus, organic carbon and particle size. In accordance of international criteria of quality of sediment, the results indicate an anthropogenic collaborations since some metals reached an excessive values. The factor of contamination was also used to evaluate the levels of contamination. The levels of Cu and Pb indicate a moderate contamination, so that its possible to do harm to the balance of the ecosystem studied.

Biomonitoramento de Cr e Pb em peixes de água doce

Trace metal content of three fish species harvested from a tank located in the City of Guarapuava-PR, Brazil were determined by digestion and voltametry. Trace metal content in fish samples were 0.10-1.30 µg/g (muscle) and 0.45-15.90 µg/g (liver) for chromium, 0.35-2.56 µg/g (muscle) and 2.32-34.30 µg/g (liver) for lead. The levels of lead and chromium in fish samples were higher than the recommended legal limits for human consumption. To assess the dietary intake of Cr and Pb by fish, weekly intake was calculated based on average metals contents and weekly consumption of fish and it compared with PTWI (Provisional Tolerable Weekly Intake). The Cr and Pb have achieved up to 25 and 45%, respectively, of PTWI recommended by WHO/FAO.

Determinação direta de crômio em açúcar e leite por espectrometria de absorção atômica com atomização eletrotérmica em forno de grafite

A fast and direct method for the determination of Cr in milk and cane sugar suspensions using graphite furnace atomic absorption spectrometry with Zeeman-effect background correction is described. No sample pre-treatment was necessary, minimizing the risk of contamination. The concentration of chromium in cane sugar was evaluated using Cr reference solutions prepared in 1% v/v HNO3 solution. The milk samples were introduced into the furnace with a mixture of amines for avoiding the autosampler blockage and foaming of milk. Chromium determination in milk was based on the standard additions method (SAM). The limit of detection and characteristic mass for cane sugar sample (30 mL) were 0,13 ng/ml and 4,3 pg, and for milk sample (10 mL) were 0,23 ng/ml and 7,8 pg, respectively. The graphite tube lifetime was 300 firings for sugar-cane sample and 100 firings for milk sample. The heating program was implemented in 68 s.

Effect of extraction solvent on antiradical activity of the obtained propolis extracts

Summary Total phenolic, flavonoid and mineral contents and antiradical activity are usually used as a measure of propolis extract quality. The purpose of this study was to compare the quality of propolis extracts obtained with different solvents such as water, ethanolic solutions (30, 70, 95%, v/v in water) and edible vegetable oils (canola and soybean). LC-MS was used to identify constituents of the extracts. Antiradical activity was assayed using chemiluminescence from the luminol/hemin/H2O2/CTAB system and the DPPH test. Both antiradical assays were strongly correlated (r = -0.97). Principal Component Analysis indicated positive correlations for phenolics, flavonoid levels and antiradical activity showing that all phenolic compounds are important for the scavenging activity of Brazilian propolis. The extract obtained with ethanol 30% v/v had the highest antiradical activity mainly due to its high content of dicaffeoylquinic acids.

Development and in house validation of a new thermogravimetric method for water content analysis in soft brown sugar.

Recently the use of brown sugar has increased due to its nutritional characteristics, thus requiring a more rigid quality control. The development of a method for water content analysis in soft brown sugar is carried out for the first time by TG/DTA with application of different statistical tests. The results of the optimization study suggest that heating rates of 5°C min(-1) and an alumina sample holder improve the efficiency of the drying process. The validation study showed that thermo gravimetry presents good accuracy and precision for water content analysis in soft brown sugar samples. This technique offers advantages over other analytical methods as it does not use toxic and costly reagents or solvents, it does not need any sample preparation, and it allows the identification of the temperature at which water is completely eliminated in relation to other volatile degradation products. This is an important advantage over the official method (loss on drying).

Clay and charcoal composites: characterisation and application of factorial design analysis for dye adsorption

The characterisation of smectite clay, charcoal and prepared clay-charcoal composites was carried out through the X-ray diffractometry, energy dispersive X-ray spectroscopy (EDS), simultaneous thermal analysis (TGA/DTA), infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The analysis revealed the composites to have different characteristics from the precursor clay and charcoal, and a peak displacement (d001) was observed through the X-ray diffraction; this suggests the incorporation of charcoal into the clay lamellas and the formation of a new phase. Tests of adsorption with methylene blue dye were also carried out to evaluate the percentage of dye removal by the adsorbent, in which the composites presented better results than charcoal, indicating great potential for industrial use. A 23 factorial design was employed to evaluate the influence of temperature, ionic strength and pH on the adsorption of methylene blue using the AV50 composite that presented the best adsorption efficiency.

A fast microwave-assisted, acid-vapor, steam-cleaning procedure for autosampler cups

Abstract A new and fast procedure is proposed for cleaning autosampler cups using acid-vapor steam-cleaning with a miniaturized assembly in a microwave-heated sealed Teflon vessel. A glass cactus-shaped holder was made to support six polyethylene autosampler cups (volume, 2.0 mL) inside a 100 mL microwave vessel. Regent-grade nitric acid was added to the vessels, and the system was heated in a microwave oven for 5 min at 300 W. Chromium was determined by graphite-furnace atomic-absorption spectrophotometry. The blank values were lower with cleaned cups compared to untreated cups (i.e., as received from supplier). The quantification limits, estimated from detection limits established with Milli-Q water, were 0.66 and 0.95 μg Cr L −1 for cleaned and untreated auto-sampler cups, respectively.

Fractionation and Potential Toxic Risk of Metals From Superficial Sediment in Itaipu Lake—Boundary Between Brazil and Paraguay

The objective of this study was to evaluate fractions of metals (labile and pseudo-total) extracted from sediment samples collected in Itaipu Lake (boundary between Brazil and Paraguay) and to assess the dynamics and mobility of these fractions by identifying the same bioavailability and ecological risk to metals in the aquatic environment. The concentrations of metal ions were determined by flame atomic absorption spectrometry. There was a correlation between the metal ions, both in the labile and the pseudo-total, with regard to particle size. To assess metals concentrations in sediment, numerical sediment-quality guidelines were applied. The concentrations of aluminum, cadmium, iron, manganese, lead, and zinc in all sediment samples are lower than the proposed probable effects level (PEL), thus possibly indicating that there are no harmful effects from these metals. In contrast, concentrations of copper, chromium, and nickel exceeded the PEL in some samples, thus indicating that these stations are at potential risk. The level of contamination in sediments of Itaipu Lake for all metals was evaluated using contamination factor, degree of contamination, and sum-of-metals toxic unit.