Carmelo G. Barroso
University of Cádiz
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Publication
Featured researches published by Carmelo G. Barroso.
Journal of Chromatography A | 2003
Mauricio A. Rostagno; Miguel Palma; Carmelo G. Barroso
Efficiency in extracting four isoflavone derivatives (daidzin, glycitin, genistin and malonyl genistin) from freeze-dried ground soybeans was compared for mix-stirring extraction and ultrasound-assisted extraction, using different solvents and extraction temperatures with both. The efficiency of the extraction of soy isoflavones was improved by ultrasound but was dependent on the solvent employed. Optimization of the ratios of sample quantity to solvent volume and length of extraction time was also performed. Isoflavones can be quantitatively extracted from soybeans with 50% ethanol at 60 degrees C using ultrasound-assisted extraction in 20 min.
Analytica Chimica Acta | 2012
Ceferino Carrera; Ana Ruiz-Rodríguez; Miguel Palma; Carmelo G. Barroso
A new ultrasound-assisted extraction method was developed for the determination of phenolic compounds present in grapes. Several extraction variables including extraction temperature (0-75°C), output amplitude (20, 50 and 100%), duty cycle (0.2 s, 0.6 s and 1 s), the quantity of sample (0.5-2 g), and the total extraction time (3-15 min) were evaluated. One of the most widely used extraction methods of polyphenol extraction has been used as reference method. Three parameters were compared: total amount of phenolic compounds, total amount of anthocyanins and total amount of tannic components. The resulting method produced similar or higher recoveries for these three parameters; however a much shorter extraction time was needed: 6 min (ultrasound assisted extraction method) instead of 60 min (reference method). Analytical properties for the new method were established, including limit of detection, limit of quantification, repeatability and reproducibility. The developed method was applied to two different types of grapes in different ripening degree.
Journal of Chromatography A | 2001
Miguel Palma; Zulema Piñeiro; Carmelo G. Barroso
The stability of nine phenolic compounds in the extraction with superheated methanol at different temperatures (40, 50, 100 and 150 degrees C) has been tested. The evolution of the same compounds in boiling methanol (65 degrees C) in contact with air was also determined. All the assayed phenolic compounds were stable under the extraction conditions with the exception of catechin and epicatechin (recoveries: 87.4% for catechin and 86.0% for epicatechin at 150 degrees C and 94.1% for epicatechin at 100 degrees C). Phenolic compounds kept at the boiling point of methanol (65 degrees C) showed lower recoveries: gentisic acid (85.5%), syringic aldehyde (92.8%), catechin (63.7%) and epicatechin (63.4%). Extraction with superheated solvents was also applied to the extraction of phenolic compounds from solid wastes of the winemaking process.
Analytica Chimica Acta | 2002
Miguel Palma; Carmelo G. Barroso
Abstract The optimization of an ultrasound-assisted extraction (UAE) method for tartaric and malic acids from grape derived samples is shown. A fractional factorial experimental design allowed for the determination of the effects of seven extraction variables. Relationships between all the variables were examined. By applying graphical analysis, the best extractions conditions were obtained. The most important variables were the extracting liquid and the extraction temperature. Later, a central composite design was applied for optimizing the temperature and the composition of the extracting liquid. The optimized method was applied to grapes and to winemaking by-products. The repeatability of the method was studied and the recovery of tartaric and malic acids was established. Organic acids quantification was done by liquid chromatography (LC) using a post-column buffer and a conductivity detector.
Talanta | 2008
Gerardo F. Barbero; Ali Liazid; Miguel Palma; Carmelo G. Barroso
The development of a rapid, reproducible and simple method of extraction of the majority capsaicinoids (nordihydrocapsaicin, capsaicin, dihydrocapsaicin, homocapsaicin and homodihydrocapsaicin) present in hot peppers by the employment of ultrasound-assisted extraction is reported. The study has covered four possible solvents for the extraction (acetonitrile, methanol, ethanol and water), the optimum temperature for extraction (10-60 degrees C), the extraction time (2-25 min), the quantity of sample (0.2-2 g), and the volume of solvent (15-50 mL). Under the optimum conditions of the method developed, methanol is employed as solvent, at a temperature of 50 degrees C and an extraction time of 10 min. The repeatability and reproducibility of the method (R.S.D.<3%) have been determined. The capsaicinoids extracted have been analysed by HPLC with fluorescence detection and using monolithic columns for the chromatographic separation. The method developed has been employed for the quantification of the various capsaicinoids present in different varieties of hot peppers cultivated in Spain.
Talanta | 2002
Miguel Palma; Carmelo G. Barroso
FT-IR spectra were employed for the differentiation and classification of wines and brandies during their ageing process, as well as for the characterisation and differentiation of distilled drinks from several producing countries. The FT-IR spectra have enabled the differentiation of the six scales of ageing of sherry wine. A good linear regression fit (regression coefficient=0.995) has been obtained between ageing scale and the data of the FT-IR spectrum. In the case of Brandy of Jerez, it has been possible to differentiate the three degrees of ageing and to devise a system of classification by means of linear discriminant analysis, with a reliability of 83%. The application of the regression by partial least squares has allowed us to obtain a regression between the degree of ageing and the data of the FT-IR spectrum (correlation coefficient=0.986). Lastly, Spanish, French and South African brandies, as well as cognacs and armagnacs have been characterised, and a complete differentiation of the latter two types from the rest of the samples of distilled drinks has been obtained.
Journal of Chromatography A | 2001
Cristina Domı́nguez; Dominico A. Guillén; Carmelo G. Barroso
A method has been developed for the simultaneous determination of resveratrol in all its forms (free isomers and glycosylates) in wines by high-performance liquid chromatography with diode array and mass spectrometric detection. Prior to injection into the column, preconcentration of the sample by automated solid-phase extraction is carried out. In the detection by UV absorption, quantitation was carried out at 280 and 305 nm, and in detection by mass spectrometry, quantitation was performed in the selected ion monitoring mode at m/z 228 and at m/z 238. A comparative study between both detection systems was carried out.
Journal of Chromatography A | 2002
Miguel Palma; Zulema Piñeiro; Carmelo G. Barroso
A new method of pressurized-fluid extraction coupled in-line with solid-phase extraction has been used for the extraction of phenolic compounds from grapes. The full extraction method is performed under an inert atmosphere. Five different solvents have been assayed using different extraction pressures and temperatures. Using two extraction stages with two different solvents, water and methanol, quantitative recovery for most of the assayed compounds has been found in the second extract. Only the most polar phenolic compound, gallic acid, was found distributed in both extracts. The application to real samples allows for a clean-up of the extracts. Cinnamic esters like caftaric acid, cis and trans-coutaric acids were found only in the methanolic extract. The reproducibility for the new method was measured using both an inert solid spiked with standards and grapes. Using between 202 and 424 microg of spiked standards, the resulting relative standard deviations were less than 5%, with the exception of gallic acid (RSD=13%). For grapes, the resulting RSD were 11% for trans-coutaric acid, 10% for caftaric acid and 6% for cis-coutaric acid.
Analytica Chimica Acta | 2002
P. Benítez; Remedios Castro; Carmelo G. Barroso
Abstract Ion exchange techniques have been used to reduce the content of iron, copper and manganese in white wines. Two exchanger resins have been compared, a chelating resin, the active group of which is iminodiacetate and a Dowex, acidic cation exchange resin. The results obtained show that the technique of using exchanger resins is extremely effective in lowering the metal content of wines, although on occasions, their use alters the organoleptic characteristics of the wine. Treated wines present lower polyphenolic and aromatic profiles than the untreated wines. Polyphenolic and metallic reductions would explain why treated wines present a notably reduced susceptibility to browning.
Analytica Chimica Acta | 2002
Cristina Domı́nguez; Dominico A. Guillén; Carmelo G. Barroso
An easy, fast and reliable analytical method is proposed to determine the concentration of volatile phenols (ethyl- and vinylphenols) in fino sherry wines. The technique employed is a single stage sample treatment by solid-phase extraction (SPE) following a simple, fast procedure that enables 12 samples to be extracted simultaneously and requires a small volume sample and little time. Subsequently, the extracts are analyzed by gas chromatography (GC) with flame ionization detection. The method proposed has been applied to the study of fino sherry wines affected by microbial contamination with yeasts of the Brettanomyces genus, and the relationship of these yeasts with the concentrations of volatile phenols present in this wine.