Biomedical subjects

A V Filgueiras

Publications and source records attributed to A V Filgueiras.

5 recordsLinked to original sources

PubMed2004

Evaluation of distribution, mobility and binding behaviour of heavy metals in surficial sediments of Louro River (Galicia, Spain) using chemometric analysis: a case study.

Contents of total and extractable heavy metals, carbonates, MnO and Fe2O3, organic matter, and matrix components such as SiO2, Al2O3, CaO, Na2O, MgO, TiO2, K2O and P2O5 are used along with principal component analysis (PCA) for studying distribution, mobility and binding behaviour of Cd, Cr, Cu, Ni and Pb in the Louro River (Galicia, Spain). Eleven surficial sediment samples were taken along the beds of the river course. Total metal concentrations were obtained after microwave-assisted digestion whilst extractable metal contents were obtained following a three-stage sequential extraction scheme (i.e. soluble, reducible and oxidisable fractions). Loading plots of heavy metals bound to carbonates, Fe-Mn oxides, organic matter and aluminosilicates allowed determination of binding behaviour. Correlations found indicate that Pb and Cu are mainly discharged from urban wastes, whereas Cr and Ni are from electroplating and galvanizing industries. The occurrence of diffuse pollution sources along the river can account for the binding behaviour of Cd. Metal mobility decreased in the order: Cd > Pb > Cu > Ni > Cr. Despite total contents indicating moderate-to-high heavy metal pollution in this river, metals are mostly distributed in the residual fraction, hence showing a low risk of mobility.

Journal Article↗

PubMed2002

Comparison of the standard SM&T sequential extraction method with small-scale ultrasound-assisted single extractions for metal partitioning in sediments.

A single extraction method based on the reagents employed in the SM&T (standards, measurement and testing programme) sequential extraction scheme for partitioning of Cd, Cr, Cu, Ni, and Pb in sediments has been developed. Small-scale extractions adapted to electrothermal atomic absorption spectrometric determinations (i.e. 25 mg mass in 1 mL extractant) have been used for the first time in conjunction with selective reagents using conventional operating conditions (i.e. conductive heating, magnetic stirring) or ultrasound-assisted extraction. Small-scale slurry preparations were implemented for determination of the residual/total metal content. The methodology developed enabled drastic reduction of extraction times, yielding extractable contents in accordance with those obtained by application of the conventional SM&T method, which can be regarded as a standard method. An important saving in the amount of sample and reagents is also achieved with small-scale extractions. Homogeneity of sediments at the mg level proved acceptable - precision was similar for between-batch and within-batch measurements. Method development was performed with CRM BCR 601 lake sediment for which extractable amounts of several metals are known. An application to a "real-world" sediment is also presented.

Journal Article↗

PubMed2002

Chemical sequential extraction for metal partitioning in environmental solid samples.

A comprehensive review of the sequential extraction schemes for metal fractionation in environmental samples (ie., sediment, soil, sewage sludge, fly ash, etc.) is presented. The review contains more than 400 references and covers principally the literature published over the last decade. The use of each reagent involved in these schemes is looked at critically, and guidelines for their selectivity and extraction capacity are given. The operational character of these schemes is emphasised. Topics such as comparability between sequential extraction schemes of widespread use, harmonisation, acceleration, validation, etc. are addressed and future developments outlined.

Chemistry Techniques, Analytical↗

PubMed2001

Ultrasound-assisted solubilization of trace and minor metals from plant tissue using ethylenediaminetetraacetic acid in alkaline medium.

A simplified and fast sample pretreatment method based on ultrasound-assisted solubilization of metals from plant tissue with ethylenediaminetetraacetic acid in alkaline medium is described. Powdered unknown and certified plant samples (particle size < 50 microns) were slurried in the solubilization medium and subjected to high intensity ultrasonication by a probe ultrasonic processor (20 kHz, 100 W). Metal solubilization can be accomplished within 3 min using a 30% vibrational amplitude and 0.1 M EDTA at pH 10, the supernatant obtained upon centrifugation being used for analysis. The method is applied to several food plants with unknown metal contents and certified plant samples such as CRM GBW07605 tea leaves, BCR CRM 61 aquatic moss and BCR CRM 482 lichen, with good trueness and precision. Intensive treatments with concentrated acids involving total matrix decomposition can be avoided. Metal determination (Ca, Cd, Mg, Mn, Pb and Zn) in the alkaline extracts was carried out by flame and electrothermal atomic absorption spectrometry.

Bryopsida↗

PubMed1999

Comparison of digestion methods for determination of trace and minor metals in plant samples.

In this paper, three dissolution methods using pressure digestion vessels (low-, medium-, and high-pressure vessels) for the determination of metals in plant samples are described. The Plackett-Burman saturated factorial design was used to identify the significant factors influencing wet ashing and to select optimized dissolution conditions. The three methods were statistically compared (on-way ANOVA) on the same sample; no significant differences were obtained. In all cases the relative standard deviation values were <3%. The digestion method based on the use of low-pressure vessels and a microwave oven was validated against CRM GBW07605 tea leaves. This method was applied to the determination of Cu, Zn, Mn, Fe, Mg, and Ca in 22 different medicinal, aromatic, and seasoning plants by flame-atomic absorption spectrometry. The concentration intervals of metal in the plants analyzed were the following: Cu, 4 (Allium sativum)-35 (Thea sinensis) microg g(-1); Zn, 7 (Piper nigrum)-90 (Betula alba) microg g(-1); Mn, 9 (Allium sativum)-939 (Caryophylus aromaticus) microg g(-1); Fe, 33 (Allium sativum)-2486 (Anethum graveolens) microg g(-1); Mg, 495 (Allium sativum)-7458 (Ocimum basilicum) microg g(-1); Ca, 386 (Allium sativum)-21500 (Ocimum basilicum) microg g(-1).

Analysis of Variance↗