Roberto Romero-González

Publications (57) View all

• Article: Analysis of veterinary drug residues in cheese by ultra-high-performance LC coupled to triple quadrupole MS/MS.

  María Luz Gómez Pérez, Roberto Romero-González, José Luis Martínez Vidal, Antonia Garrido Frenich
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  ABSTRACT: A simple, reliable, and fast multiresidue method has been developed for the determination of 17 veterinary drugs belonging to several families (macrolides, sulfonamides, and anthelmintics) in cheese at trace levels. Ultra-high-performance LC coupled to MS/MS has been used for the analysis of these compounds in less than 9 min. Veterinary drug residues have been extracted from cheese samples using a QuEChERS (quick, easy, cheap, effective, rugged, and safe)-based extraction procedure without applying any further clean-up step. Matrix-matched calibration was used for quantification and recoveries were calculated at three concentration levels (10, 50, and 100 μg/kg). The obtained values ranged from 70 to 110% for the selected compounds except for tylosin and josamycin at 100 μg/kg (111.7 and 112.7%, respectively). Intra- and interday precision were also evaluated and RSDs were lower than 25% in all the cases. LOQs ranged from 0.3 μg/kg (for thiabendazole, oxfendazole, mebendazole, josamycin, and fenbendazole) to 10.5 μg/kg (abamectin), whereas decision limit and detection capability ranged from 2.3 (thiabendazole) to 11.3 (abamectin) and 4.2 (thiabendazole) to 14.3 μg/kg (abamectin), respectively. Finally, 13 samples were analyzed and traces of thiabendazole were detected in two different cheeses.
  Journal of Separation Science 04/2013; 36(7):1223-30. · 2.73 Impact Factor
• Article: Systematic study of the contamination of wastewater treatment plant effluents by organic priority compounds in Almeria province (SE Spain).

  Nieves Barco-Bonilla, Roberto Romero-González, Patricia Plaza-Bolaños, José L Martínez Vidal, Antonia Garrido Frenich
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  ABSTRACT: The occurrence of priority organic pollutants in wastewater (WW) effluents was evaluated in a semi-arid area, characterized by a high agricultural and tourism activity, as Almeria province (Southeastern Spain). Twelve wastewater treatment plants (WWTPs) were sampled in three campaigns during 2011, obtaining a total of 33 WW samples, monitoring 226 compounds, including pesticides, polycyclic aromatic hydrocarbons (PAHs), phenolic compounds and volatile organic compounds (VOCs). Certain banned organochlorine pesticides such as aldrin, pentachlorobenzene, o,p'-DDD and endosulfan lactone were found, and the most frequently detected pesticides were herbicides (diuron, triazines). PAHs and VOCs were also detected, noting that some of these pollutants were ubiquitous. Regarding phenolic compounds, 4-tertoctylphenol was found in all the WW samples at high concentration levels (up to 89.7μg/L). Furthermore, it was observed that WW effluent samples were less contaminated in the second and third sampling periods, which corresponded to dry season. This evaluation revealed that despite the WW was treated in the WWTP, organic contaminants are still being detected in WW effluents and therefore they are released into the environment. Finally the risk of environmental threat due to the presence of some compounds in WWTP effluents, especially concerning 4-tertoctylphenol must be indicated.
  Science of The Total Environment 03/2013; 447:381-9. · 3.29 Impact Factor
• Article: Innovative determination of polar organophosphonate pesticides based on high-resolution Orbitrap mass spectrometry.

  Juan Antonio Padilla-Sánchez, Patricia Plaza-Bolaños, Roberto Romero-González, Angel Grande-Martínez, Earl Michael Thurman, Antonia Garrido-Frenich
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  ABSTRACT: The determination of compounds showing a very low molecular weight (i.e. < 200 Da) can be complicated when low-resolution mass spectrometry is used in the selected-reaction monitoring mode, since the possible number of product ions is reduced and the obtained reactions are not selective enough to overcome background noise and/or matrix interferences. In this study, the use of high-resolution mass spectrometry based on Exactive Orbitrap was applied for the determination of a group of polar organophosphonate pesticides and transformation products (TPs), which show the aforementioned features, in agricultural soils. Namely, glyphosate, glufosinate, ethephon and their TPs, aminomethyl phosphonic acid (AMPA), 3-methylphosphinicopropionic acid, N-acetyl-glufosinate and 2-hydroxyethylphosphonic acid were analyzed. The [M-H](-) ions 168.00564, 180.04202, 142.96593, 110.00016, 151.01547, 222.05259 and 124.99982 were used, respectively, for the detection and identification of the compounds. Confirmation was carried out by using accurate mass measurements of ion fragments for each compound, from neutral losses of CO(2) , H(2) O and H(2) CO (formaldehyde). Furthermore, the recently reported tool, relative isotopic mass defect (RΔm), was also used to support the confirmation protocol. The optimized method was fully validated at low levels, including the estimation of a not commonly used parameter: the limit of confirmation (LOC). This LOC is expressed as the lowest concentration of compound that can be confirmed using a fragment or the RΔm, and it ranged from 10 to 50 µg kg(-1) for all compounds. All the data was obtained in a single injection. Finally, the method was applied to real soil samples, and glyphosate and AMPA were found at 265 µg kg(-1) and 105 µg kg(-1) , respectively. Copyright © 2012 John Wiley & Sons, Ltd.
  Biological Mass Spectrometry 11/2012; 47(11):1458-65. · 3.41 Impact Factor
• Article: Analysis of phenolic compounds in olive oil by solid-phase extraction and ultra high performance liquid chromatography-tandem mass spectrometry.

  María Isabel Alarcón Flores, Roberto Romero-González, Antonia Garrido Frenich, José Luis Martínez Vidal
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  ABSTRACT: In this study a simultaneous determination of several classes of polyphenolic compounds (benzoic acid derivates, cinnamic acid derivates, phenyl ethyl alcohols, flavones and other phenolic acids) in feed oils has been carried out by ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). Solid-phase extraction (SPE) with Diol and C(18) cartridges were compared in terms of recovery and number of extracted compounds, obtaining better results when Diol cartridges were used. The analytical procedure was validated, obtaining recoveries ranging from 70% (vanillic acid) to 111% (gallic acid) with repeatability values (expressed as relative standard deviations, RSDs) lower than 20% at two concentration levels (500 and 1000μg/kg). Limits of quantification (LOQs) were always equal or lower than 50μg/kg except for gentisic acid (100μg/kg). Finally the method was applied to different types of feed oils, and it can be observed that higher concentrations of polyphenols were found in olive oil, whereas pomace olive oil and sunflower oil had the lowest level of these compounds.
  Food Chemistry 10/2012; 134(4):2465-72. · 3.65 Impact Factor
• Article: Comprehensive qualitative and quantitative determination of pesticides and veterinary drugs in honey using liquid chromatography-Orbitrap high resolution mass spectrometry.

  María Luz Gómez-Pérez, Patricia Plaza-Bolaños, Roberto Romero-González, José Luis Martínez-Vidal, Antonia Garrido-Frenich
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  ABSTRACT: A database has been created for the simultaneous analysis of more than 350 pesticides and veterinary drugs (including antibiotics) using ultra-high performance liquid chromatography coupled to high resolution Orbitrap mass spectrometry (UHPLC-Orbitrap-MS). This is a comprehensive exact mass database built using the Exactive-Orbitrap analyzer. The developed database includes exact masses of the target ions and retention time data, and allows the automatic search of the included compounds. Generic chromatographic and MS conditions have been applied. The presented database is suitable for qualitative analysis, and it was also evaluated for quantitative purposes in routine analysis, after the optimization and validation of a generic extraction method in honey samples. Adequate recovery and precision values for most of the studied analytes were obtained and the limits of detection (LOD) ranged from 1 to 50 μg kg(-1). For pesticides, LODs were always lower than the MRLs established by European Union in honey, except for a few compounds. This method was applied to the analysis of 26 real honey samples and some pesticides (azoxystrobin, coumaphos, dimethoate and thiacloprid) were detected in 4 samples. Azoxystrobin and coumaphos were determined in two different samples (organic honey) at 1.5 μg kg(-1) and 5.1 μg kg(-1). Veterinary drugs were not detected in the analyzed samples.
  Journal of chromatography. A 06/2012; 1248:130-8. · 4.19 Impact Factor