共查询到20条相似文献,搜索用时 31 毫秒
1.
2.
Angela Paoloni Michele Solfrizzo Rita Bibi 《Journal of environmental science and health. Part. B》2018,53(5):327-333
The objective of this study was to develop a liquid chromatography tandem mass spectrometry (LC-MS/MS) method for the determination of Ochratoxin A (OTA) and Ochratoxin α (OTα) in poultry tissues and eggs. The two toxins were extracted by a mixture of acetonitrile/water, purified with a reversed phase C18 solid phase extraction column (SPE) and determined by LC-MS/MS. The LC-MS/MS method performances were evaluated in terms of linearity in solvent and in matrix (ranged from 0.5 to 15.10 µg L?1 for OTA and from 0.60 to 17.85 µg L?1 for OTα), limit of detection (LOD), limit of quantitation (LOQ), specificity, accuracy and precision in repeatability conditions. Recovery experiments were performed by spiking poultry liver, kidney, muscle and eggs around 1 µg kg?1 and 10 µg kg?1. LODs were 0.27 and 0.26 µg kg?1 while LOQs were fixed at 1.0 and 1.2 µg kg?1 for OTA and OTα, respectively. Main recoveries for OTA ranged from 82 to 109% and for OTα ranged from 55 to 89%. The values of within-laboratory relative standard deviation (RSDr) were equal to or below 20%. Considering the results obtained and that all analytical performance criteria were fulfilled, the new extraction and purification method developed for OTA and OTα determination in animal tissues and eggs was found appropriate for control laboratories and research activities designed to ensure food safety. 相似文献
3.
Karina M. Tonon Geovana D. Savi 《Journal of environmental science and health. Part. B》2013,48(10):685-691
ABSTRACTAn analytical method based on liquid chromatography–tandem mass spectrometry (LC–MS/MS) was validated and applied for the analysis of aflatoxin M1 (AFM1), ochratoxin A (OTA) and deoxynivalenol (DON) in infant formula and milk-based products for young children commercialized in Brazil. A total of 38 samples were evaluated, including 12 infant formula, 14 follow-on formula and 12 samples of milk-based products. AFM1 was detected in 12 (32%) samples, and seven (18%) samples contained AFM1 levels above the method limit of quantification in a concentration range between 0.013 and 0.067 ng mL?1 (0.026 ± 0.019). Two samples of milk-based products exceeded the maximum level (ML) fixed by the European Union for AFM1 in baby foods, however, all samples were in agreement with the levels established by the Brazilian regulation. OTA and DON were not detected in any of the analyzed samples. 相似文献
4.
5.
Angela Paoloni Sabrina Alunni Alessandro Pelliccia 《Journal of environmental science and health. Part. B》2016,51(3):133-142
A simple and straightforward method for simultaneous determination of residues of 13 pesticides in honey samples (acrinathrin, bifenthrin, bromopropylate, cyhalothrin-lambda, cypermethrin, chlorfenvinphos, chlorpyrifos, coumaphos, deltamethrin, fluvalinate-tau, malathion, permethrin and tetradifon) from different pesticide classes has been developed and validated. The analytical method provides dissolution of honey in water and an extraction of pesticide residues by n-Hexane followed by clean-up on a Florisil SPE column. The extract was evaporated and taken up by a solution of an injection internal standard (I-IS), ethion, and finally analyzed by capillary gas chromatography with electron capture detection (GC-µECD). Identification for qualitative purpose was conducted by gas chromatography with triple quadrupole mass spectrometer (GC-MS/MS). A matrix-matched calibration curve was performed for quantitative purposes by plotting the area ratio (analyte/I-IS) against concentration using a GC-µECD instrument. According to document No. SANCO/12571/2013, the method was validated by testing the following parameters: linearity, matrix effect, specificity, precision, trueness (bias) and measurement uncertainty. The analytical process was validated analyzing blank honey samples spiked at levels equal to and greater than 0.010 mg/kg (limit of quantification). All parameters were satisfactorily compared with the values established by document No. SANCO/12571/2013. The analytical performance was verified by participating in eight multi-residue proficiency tests organized by BIPEA, obtaining satisfactory z-scores in all 70 determinations. Measurement uncertainty was estimated according to the top-down approaches described in Appendix C of the SANCO document using the within-laboratory reproducibility relative standard deviation combined with laboratory bias using the proficiency test data. 相似文献
6.
Poirier Larabie Sylvie Jutras Martin Leclair Grégoire St-Jean Isabelle Kleinert Christine Gagné François Gagnon Christian 《Environmental science and pollution research international》2022,29(30):45303-45313
Environmental Science and Pollution Research - Aquatic organisms are continuously exposed to emerging contaminants coming from urban effluents of wastewater treatment plants. The contamination of... 相似文献
7.
8.
9.
10.
Matthaios P. Kavvalakis Manolis N. Tzatzarakis Eleftheria P. Theodoropoulou Emmanouil G. Barbounis Andreas K. Tsakalof Aristidis M. Tsatsakis 《Chemosphere》2013
Imidacloprid (IMI) is a relatively new neuro-active neonicotinoid insecticide and nowadays one of the largest selling insecticides worldwide. In the present study a LC–APCI–MS based method was developed and validated for the quantification of imidacloprid and its main metabolite 6-chloronicotinic acid (6-CINA) in urine and hair specimens. The method was tested in biomonitoring of intentionally exposed animals and subsequently applied for biomonitoring of Cretan urban and rural population. 相似文献
11.
12.
氯苯和氯酚是生活垃圾焚烧过程产生的重要污染物,目前对垃圾焚烧炉飞灰中氯苯和氯酚的研究较少。本文采用超声萃取法结合GC-ECD、LC-MS/MS,建立了飞灰等固体介质中的氯苯氯酚的定量检测方法,通过实验确定出较优的前处理条件,飞灰样品中滴加少量浓硫酸,以正己烷/丙酮(1:1)为萃取溶剂,40℃超声萃取20 min,萃取3次,然后液相萃取分离氯酚氯苯,分别净化,浓缩,最后进机检测,对三、四、五、六氯代苯和所有的氯酚均获得较好的回收率。应用建立的检测方法测试了3座正常运行过程中的生活垃圾焚烧炉飞灰的氯苯和氯酚含量,样品中一到四氯代氯酚的含量都在定量限以下,五氯酚含量范围为5~11 ng·g-1,三氯苯、四氯苯、五氯苯和六氯苯的含量在3~70 ng·g-1的范围。 相似文献
13.
14.
15.
16.
Urszula Kotowska Justyna Kapelewska Joanna Sturgulewska 《Environmental science and pollution research international》2014,21(1):660-673
A method combining ultrasound-assisted emulsification–microextraction (USAEME) with gas chromatography–mass spectrometry (GC–MS) was developed for simultaneous determination of four acidic pharmaceuticals, ibuprofen, naproxen, ketoprofen, and diclofenac, as well as four phenols, 4-octylphenol, 4-n-nonylphenol, bisphenol A, and triclosan in municipal wastewaters. Conditions of extraction and simultaneous derivatization were optimized with respect to such aspects as type and volume of extraction solvent, volume of derivatization reagent, kind and amount of buffering salt, location of the test tube in the ultrasonic bath, and extraction time. The average correlation coefficient of the calibration curves was 0.9946. The LOD/(LOQ) values in influent and effluent wastewater were in the range of 0.002–0.121/(0.005–0.403) μg L?1 and 0.002–0.828/(0.006–2.758) μg L?1, respectively. Quantitative recoveries (≥94 %) and satisfactory precision (average RSD 8.2 %) were obtained. The optimized USAEME/GC–MS method was applied for determination of the considered pharmaceuticals and phenols in influents and treated effluents from nine Polish municipal wastewater treatment plants. The average concentration of acidic pharmaceuticals in influent and effluent wastewater were in the range of 0.06–551.96 μg L?1 and 0.01–22.61 μg L?1, respectively, while for phenols were in the range of 0.03–102.54 μg L?1 and 0.02–10.84 μg L?1, respectively. The removal efficiencies of the target compounds during purification process were between 84 and 99 %. 相似文献
17.
《Atmospheric environment(England)》1984,18(5):937-951
A combined transport/chemistry model which simulates the regional distribution of SO2 and sulfate within the lower troposphere is described. The mathematical analysis is based on the coupled three-dimensional advection-diffusion equations for SO2 and sulfate, and incorporates chemical transformations as well as the physical phenomena of dry deposition at the surface. The analysis also considers spatial variations in topography and spatial and temporal variations in both the mixing layer heights and the wind field. Based on the results from a series of numerical experiments, the dynamic model employs a Galerkin method for the numerical solution of the partial differential equations.A SO2 photochemical oxidation mechanism is incorporated into the transport model. The SO2 photochemical oxidation rate is based on a set of 27 reactions used to estimate the hydroxyl and peroxyl radical concentrations. The kinetic mechanism has been tested in simulations of smog chamber studies and yields realistic concentrations and conversion rates in model simulations of both urban and natural tropospheres.Other major facets treated in the formulation of the model include the interpretation and use of data available on dry deposition and the development of procedures to calculate meteorological model inputs (e.g., eddy diffusivities, dry deposition velocities, the three components of wind velocity, etc.) from routinely measured meteorological data. Simulations using the analysis are presented in a companion paper. 相似文献
18.
19.
GC—MS方法测定垃圾焚烧炉飞灰中的二恶英 总被引:4,自引:0,他引:4
采用索氏抽提,多级硅胶/氧化铝柱层析等预处理方法,提纯分离出垃圾焚烧炉飞灰中的恶英并进行GC-MS分析,检出所测样品中存在的6 ̄8个氯取代的二恶英。 相似文献
20.
Hua-Yun Xiao Cong-Guo Tang Hong-Wei Xiao Yan-Li Wang Xue-Yan Liu Cong-Qiang Liu 《Environmental pollution (Barking, Essex : 1987)》2010,158(5):1726-1732
In urban cities in Southern China, the tissue S/N ratios of epilithic mosses (Haplocladium microphyllum), varied widely from 0.11 to 0.19, are strongly related to some atmospheric chemical parameters (e.g. rainwater SO42−/NH4+ ratios, each people SO2 emission). If tissue S/N ratios in the healthy moss species tend to maintain a constant ratio of 0.15 in unpolluted area, our study cities can be divided into two classes: class I (S/N > 0.15, S excess) and class II (S/N < 0.15, N excess), possibly indicative of stronger industrial activity and higher density of population, respectively. Mosses in all these cities obtained S and N from rainwater at a similar ratio. Sulphur and N isotope ratios in mosses are found significantly linearly correlated with local coal δ34S and NH4+-N wet deposition, respectively, indicating that local coal and animal NH3 are the major atmospheric S and N sources. 相似文献