Determination of Emerging Contaminants in Cereals by Gas Chromatography-Tandem Mass Spectrometry.

Cereals are staple foods for human consumption in both developed and developing countries. In order to improve agricultural outputs, resources like reclaimed water for irrigation and biosolids and manure as fertilizers are frequently used, although they may increase the input of contaminants that can potentially be absorbed by crops and enter the food chain. Emerging contaminants (human and veterinary pharmaceuticals, personal care products, surfactants, plasticizers, and industrial additives, among others) are continuously introduced in the environment from a variety sources and these contaminants may enter the food chain through plant uptake. In this study, an analytical method, based on ultrasound-assisted extraction and dispersive solid-phase cleanup, was developed for the determination of emerging contaminants from different classes in four highly consumed cereal grains (wheat, oat, barley, and rice). These analytes were selected considering the results of our previous studies carried out in soil and vegetables and those frequently detected in real samples were chosen. The target compounds selected were bisphenol A (BPA), bisphenol F (BPF), methyl paraben, propyl paraben, linear chain nonylphenol in position 4 (4-n-NP), mixture of ring and chain isomers of NP and six pharmaceutical compounds (allopurinol, mefenamic acid, carbamazepine, paracetamol, diclofenac and ibuprofen). Recoveries ranging from 68 to 119% with relative standard deviations (RSD) <18% were obtained for all the compounds except for allopurinol, with recoveries that ranged from 30 to 66% with RSD ≤ 12% and the limits of detection achieved ranged from 0.03 to 4.9 ng/g. The method was applied to the analysis of 16 cereal samples, ten were purchased in local supermarkets and the rest were collected directly from agricultural fields, five of which were fertilized with organic amendments. Bisphenol A (BPA) was detected in all samples at levels that ranged from 1.6 to 1,742 ng/g. Bisphenol F, a substitute for BPA, was also found in six samples (up to 22 ng/g). Linear 4-n-NP was found in a reduced number of samples but the mixture of NP isomers was found in all the samples, being the mean concentrations in wheat, barley, oat and rice 49, 90, 142, and 184 ng/g, respectively.

Analysis of emerging organic contaminants in poultry manure by gas chromatography-tandem mass spectrometry.

A multiresidue method was developed for the determination of 19 emerging organic contaminants (pharmaceutical drugs, personal care products, and bisphenol A) in poultry manure. Lyophilized samples of manure were extracted by ultrasound-assisted matrix solid-phase dispersion and the extracts were analyzed by gas chromatography with tandem mass spectrometry after derivatization. Analysis of spiked poultry manure samples, at levels ranging from 25 to 150 ng/g, gave satisfactory recovery results for all the compounds, with values from 67 to 106%. The developed procedure provided detection limits that ranged from 0.9 to 2.2 ng/g. Finally, the validated method was applied to poultry manure samples collected from 23 poultry farms in Spain. Salicylic acid was found in most of the samples analyzed at levels up to 2501 ng/g, whereas, methyl paraben, orthophenylphenol, ibuprofen, paracetamol, and carbamazepine were detected at levels up to 250 ng/g. Composting of manure showed an important decrease in the levels of the detected contaminants.

Determination of endocrine-disrupting compounds in water samples by magnetic nanoparticle-assisted dispersive liquid-liquid microextraction combined with gas chromatography-tandem mass spectrometry.

A rapid extraction procedure is presented for the determination of five endocrine-disrupting compounds, estrone, ethinylestradiol, bisphenol A, triclosan, and 2-ethylhexylsalicylate, in water samples. The analysis involves a two-step extraction procedure that combines dispersive liquid-liquid microextraction (DLLME) with dispersive micro-solid phase extraction (D-µ-SPE), using magnetic nanoparticles, followed by in situ derivatization in the injection port of a gas chromatograph coupled to triple quadrupole mass spectrometry. The use of uncoated or oleate-coated Fe3O4 nanoparticles as sorbent in the extraction process was evaluated and compared. The main parameters involved in the extraction process were optimized applying experimental designs. Uncoated Fe3O4 nanoparticles were selected in order to simplify and make more cost-effective the procedure. DLLME was carried out at pH 3, during 2 min, followed by the addition of the nanoparticles for D-µ-SPE employing 1 min in the extraction. Analysis of spiked water samples of different sources gave satisfactory recovery results for all the compounds with detection limits ranging from 7 to 180 ng l-1. Finally, the procedure was applied in tap, well, and river water. Graphical abstract Diagram of the extraction method using magnetic nanoparticles (MNPs).

Application of magnetic iron oxide nanoparticles for the analysis of PCBs in water and soil leachates by gas chromatography-tandem mass spectrometry.

Two magnetic solid-phase extraction methods (mSPE) were developed and compared for the extraction and preconcentration of polychlorinated biphenyls (PCBs) from water and soil leachates. Analyses were carried out by gas chromatography coupled to triple quadrupole mass spectrometry. The mSPE extraction parameters were optimised using Fe3O4 nanoparticles coated with palmitate or oleate. Differences were found between the developed mSPE methods depending on the magnetic nanoparticle coating. The extraction efficiency of both sorbents was studied by spiking soil leachates at three concentration levels (from 0.6 to 0.18 ng ml(-1) and from 0.4 to 0.04 ng ml(-1) using palmitate or oleate coated nanoparticles, respectively) and recoveries from 86 to 109 % were obtained. The developed method provided a preconcentration factor of 250. The detection limits were about 29 times lower with the oleate-coated nanoparticles. Although both mSPE procedures could be used for the extraction of PCBs from water and soil leachates, oleate-coated nanoparticles gave the best extractive conditions and lower quantifications limits. Finally, the mSPE using oleate-coated nanoparticles was applied to the analysis of PCBs in river waters and in soil leachates obtained from soil with different physico-chemical characteristics. The levels of PCBs present in the leachates depended on the soil sample. The present work demonstrates the applicability of both mSPE methods to the determination of PCBs in water and soil leachates, which is of interest for mobility and bioavailability studies of these compounds in soil.

Gas chromatography-triple-quadrupole mass spectrometry for analysis of selected polyhalogenated pollutants in plants. Comparison of extraction methods.

Different extraction methods, followed by gas chromatography coupled to triple quadrupole mass spectrometry, were evaluated for simultaneous extraction of seven polychlorinated biphenyls (PCBs) and six polybrominated diphenyl ethers (PBDEs) from common weeds. Pressurized liquid extraction (PLE) with in-cell clean-up, ultrasound-assisted extraction (UAE) with in-column clean-up, and UAE with dispersive solid-phase extraction (dSPE) clean-up were evaluated and compared. In-cell clean-up with 4 g Florisil and 0.5 g graphitized carbon black (GCB) and two extraction cycles of 10 min with n-hexane-ethyl acetate 80:20 (v/v) at 60 °C were used for the PLE procedure. UAE with in-column clean-up was conducted under conditions similar to those reported for the PLE method whereas in UAE with dSPE clean-up purification of the extract was performed after extraction using primary and secondary amine sorbent (PSA) and GCB. Recovery from 82 to 104% was obtained for all the compounds by PLE whereas, in general, lower extraction efficiency was obtained by UAE with in-column clean-up (especially for BDE-17 and BDE-183, for which recovery was 70 and 41%, respectively) and by UAE with dSPE clean-up, for which the main drawback is that BDE-183 cannot be extracted. Finally, PLE was used for analysis of PCBs and PBDEs in different plants (Lolium rigidum, Lactuca serriola, Malva sylvestris, and Verbascum thapsus) collected from residential and/or rural areas of Madrid (Spain). Several of the analyzed compounds were detected at low levels in these plants, but only PCB-153 could be quantified.

Composition and antioxidant activity of Trigona carbonaria honey from Australia.

Stingless bees (Tribe Meliponini) are a diverse group of highly eusocial bees distributed throughout the tropics and subtropics. Trigona carbonaria honey, from Australia, was characterized by traditional physicochemical parameters (acidity, sugars, diastase, electrical conductivity, hydroxymethylfurfural, invertase, nitrogen, and water content) and other compositional factors (flavonoids, polyphenols, organic acids, and water activity), as well as total antioxidant capacity and radical scavenging activity. For the Australian T. carbonaria, the traditional analytical parameters were similar to those previously reported for neotropical stingless bee honey and confirm that honeys produced by Meliponini bees possess several physicochemical properties that are distinctly different from Apis mellifera honey, with higher values of moisture (26.5 +/- 0.8 g of water/100 g of honey), water activity (0.74 +/- 0.01), electrical conductivity (1.64 +/- 0.12 mS/cm), and free acidity (124.2 +/- 22.9 mEq/kg of honey) and a very low diastase activity (0.4 +/- 0.5 diastase number) and invertase activity (5.7 +/- 1.5 invertase number). The sugar spectrum was quite different from that of A. mellifera honey, with 20.3 +/- 2.9 g of maltose/100 g of honey. The values of pH (4.0 +/- 0.1), lactonic acidity (4.7 +/- 0.8 mEq/kg of honey), sucrose (1.8 +/- 0.4 g/100 g of honey), and fructose/glucose ratio (1.42 +/- 0.13) fell in the same ranges as those of A. mellifera honey. Citric (0.23 +/- 0.09) and malic (0.12 +/- 0.03) acid concentrations (in g/kg of honey) of T. carbonaria honeys were in the range described for A. mellifera honey. D-Gluconic was more concentrated (9.9 +/- 1.3 g/kg of honey), in the range of Italian Castanea, Thymus, Arbutus, and honeydew honeys. Flavonoid content was 10.02 +/- 1.59 mg of quercetin equivalents/100 g of honey, and polyphenol contents were 55.74 +/- 6.11 mg of gallic acid equivalents/100 g of honey. The antioxidant activity, expressed as percentage of 2,2'-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid) cation (ABTS(*+)) decolorization, was 233.96 +/- 50.95 microM Trolox equivalents, and free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH(*)) depletion was 48.03 +/- 12.58 equivalents of ascorbic acid. All reported values are averages +/- standard deviation. The antioxidant activity can represent an important added value for T. carbonaria honey, to initiate a medicinal approach for both nutritional and pharmaceutical applications, besides further physicochemical characterization.

Amino acid composition and antioxidant capacity of Spanish honeys.

The amino acid composition of 53 honey samples from Spain, consisting of 39 floral, 5 honeydew, and 9 blend honeys, has been determined. Physicochemical characteristics, polyphenolic content, amino acid composition, and estimation of the radical scavenging capacity against the stable free radical DPPH of the honey samples were analyzed. The resulting data have been statistically evaluated. The results showed that pH, acidity, net absorbance, electrical conductivity, and total polyphenolic contents of the honeys showed a strong correlation with the radical scavenging capacity. The correlation between the radical scavenging capacity of honey and amino acid contents was high with 18 of the 20 amino acids detected, with correlation values higher than those obtained for polyphenolic content. These results suggest that the amino acid composition of honey is an indicator of the sample's scavenging capacity.