Search results for "Aromatic hydrocarbon"

showing 10 items of 155 documents

Efficacy of Ozonation Treatments of Smoked Fish for Reducing Its Benzo[a]pyrene Concentration and Toxicity

2017

Ozone is widely used in food processing, for example, to decompose mycotoxins or pesticide residues, to extend the shelf life of products, and for sanitation. The objective of this study was to assess the possibility of expanding the application of ozone for oxidative degradation of polycyclic aromatic hydrocarbons (PAHs). The evaluation was conducted by ozonation of a benzo[a]pyrene (BaP) standard solution and smoked fish (sprats) contaminated with PAHs. The effect of ozonation was immediate in the BaP solution; 89% of this toxic compound was decomposed after only 1 min of treatment. However, the impact of ozonation on the smoked sprats was less pronounced, even after prolonged treatment. …

ChryseneFood Handling010501 environmental sciencesShelf life01 natural sciencesMicrobiologychemistry.chemical_compound0404 agricultural biotechnologySmokeBenzo(a)pyrenepolycyclic compoundsAnimalsHumansOrganic chemistryPolycyclic Aromatic Hydrocarbons0105 earth and related environmental sciencesFluorantheneFluorenesPesticide residueChemistryFishes04 agricultural and veterinary sciences040401 food scienceSmoked fishBenzo(a)pyreneEnvironmental chemistryToxicityPyreneFood ScienceJournal of Food Protection
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Extraction of polycyclic aromatic hydrocarbons from cookies: a comparative study of ultrasound and microwave-assisted procedures.

2008

The chromatographic determination of 15 polycyclic aromatic hydrocarbons (PAHs) in cookies has been improved in order to obtain a fast method with a low limit of detection through the combination of microwave-assisted extraction (MAE), oil saponification and solid-phase extraction clean-up before the injection of purified extracts in a C18 201TP52 (5 microm, 250 x 2.1 mm) column. Using acetonitrile-water as mobile phase, with a 50% to 95% w/w acetonitrile gradient for a fixed flow of 0.250 ml min(-1), 15 PAHs were separated in 45 min. The column temperature was maintained at 15 degrees C; and fluorimetric detection was made at a fixed excitation wavelength of 264 nm and emission measurement…

ChryseneHealth Toxicology and MutagenesisFlourAnalytical chemistryFood ContaminationFluoreneToxicologyHigh-performance liquid chromatographychemistry.chemical_compoundFood IndustryFluorometryUltrasonicsSolid phase extractionPolycyclic Aromatic HydrocarbonsMicrowavesChromatography High Pressure LiquidDetection limitChromatographyExtraction (chemistry)Solid Phase ExtractionPublic Health Environmental and Occupational HealthGeneral ChemistryGeneral MedicineToluenechemistryPyreneFood ScienceFood additivescontaminants. Part A, Chemistry, analysis, control, exposurerisk assessment
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Microsomal activation of dibenzo[def,mno]chrysene (anthanthrene), a hexacyclic aromatic hydrocarbon without a bay-region, to mutagenic metabolites.

2002

Metabolically formed dihydrodiol epoxides in the bay-region of polycyclic aromatic hydrocarbons are thought to be responsible for the genotoxic properties of these environmental pollutants. The hexacyclic aromatic hydrocarbon dibenzo[def,mno]chrysene (anthanthrene), although lacking this structural feature, was found to exhibit considerable bacterial mutagenicity in histidine-dependent strains TA97, TA98, TA100, and TA104 of S. typhimurium in the range of 18-40 his(+)-revertant colonies/nmol after metabolic activation with the hepatic postmitochondrial fraction of Sprague-Dawley rats treated with Aroclor 1254. This mutagenic effect amounted to 44-84% of the values determined with benzo[a]py…

ChryseneMaleSalmonella typhimuriumStereochemistryAnthanthreneToxicologyRats Sprague-Dawleychemistry.chemical_compoundmedicineAnimalsBenzopyreneschemistry.chemical_classificationStrain (chemistry)Mutagenicity TestsGeneral MedicineChlorodiphenyl (54% Chlorine)RatschemistryEnzyme InductionPhenobarbitalMicrosomeMicrosomes LiverPyrenePhenobarbitalAromatic hydrocarbonAfter treatmentNADPmedicine.drugMethylcholanthreneMutagensChemical research in toxicology
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Covalent DNA adducts formed by benzo[c]chrysene in mouse epidermis and by benzo[c]chrysene fjord-region diol epoxides reacted with DNA and polynucleo…

1997

The metabolic activation in mouse skin of benzo[c]chrysene (B[c]C), a weakly carcinogenic polycyclic aromatic hydrocarbon (PAH) present in coal tar and crude oil, was investigated. Male Parkes mice were treated topically with 0.5 mumol of B[c]C, and DNA was isolated from the treated areas of skin at various times after treatment and analyzed by 32P-postlabeling. Seven adduct spots were detected, at a maximum level of 0.89 fmol of adducts/microgram of DNA. Four B[c]C-DNA adducts persisted in skin for at least 3 weeks. Treatment of mice with 0.5 mumol of the optically pure putative proximate carcinogens (+)- and (-)-trans-benzo[c]chrysene-9,10-dihydrodiols [(+)- and (-)-B[c]C-diols] led to th…

ChryseneMaleStereochemistryPolynucleotidesToxicologyAdductchemistry.chemical_compoundDNA AdductsMiceAnimalsCarcinogenBiotransformationChromatography High Pressure LiquidSkinCarcinogenic Polycyclic Aromatic HydrocarbonSingle-Strand Specific DNA and RNA EndonucleasesAbsolute configurationGeneral MedicineDNAPhenanthreneschemistryCovalent bondPolynucleotideAutoradiographyEpoxy CompoundsSpectrophotometry UltravioletChromatography Thin LayerDNAChemical research in toxicology
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Glutathione Transferase A1-1 Catalyzed Conjugation of Polycyclic Aromatic Hydrocarbon Diol-Epoxides with Glutathione

1996

Abstract The glutathione transferase A1-1 (GSTA1-1) isoenzyme catalyzes the formation of GSH-conjugates of the isomeric bay-region diol-epoxides (DEs) of trans-1,2-dihydroxy-3,4-epoxy-1,2,3,4-tetrahydrochrysene (CDE) and trans-3,4-dihydroxy-1,2-epoxy-1,2,3,4-tetrahydrodibenz[a,h]anthracene (DBADE) as well as the isomeric fjord-region DEs trans-3,4-dihydroxy-1,2-epoxy-1,2,3,4-tetrahydrobenzo[c]phenanthrene (BPhDE) and trans-9,10-dihydroxy-11,12-epoxy-9,10,11,12-tetrahydro-benzo[c]chrysene (BCDE) although with an approx. 20-fold variation in catalytic efficiency. With the anti-diastereomers and the syn-diastereomers of BPhDE and BCDE, GSTA1-1 demonstrated a significant preference for the enan…

Chrysenechemistry.chemical_classificationAnthracenePolymers and PlasticsStereochemistryOrganic ChemistryPolycyclic aromatic hydrocarbonGlutathionePhenanthreneConjugated systemCatalysischemistry.chemical_compoundchemistryMaterials ChemistryOrganic chemistryEnantiomerPolycyclic Aromatic Compounds
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Molecular analysis of the catechol-degrading bacterial community in a coal wasteland heavily contaminated with PAHs

2010

International audience; A PCR-based molecular tool was developed to estimate the diversity of the catechol-degrading bacterial community in a coal wasteland heavily contaminated with PAHS. A degenerate primer pair specific to catA sequences was designed by multiple alignment of known sequences coding a key intermediate of the β-ketoadiapate pathway degrading catechol, namely catechol 1,2-dioxygenase. The specificity of this primer pair was assessed in 21 pure strains by PCR and sequencing. Comparison of the 16S rDNA and catA phylogenies revealed an absence of congruence between these two genes. The primer set was able to amplify catA sequences in DNA extracts from an industrial soil highly …

DNA BacterialEnvironmental Engineering[SDV]Life Sciences [q-bio]Health Toxicology and MutagenesisCatecholsIndustrial WasteBACTERIAL COMMUNITYActinobacteriaSOIL DNA03 medical and health sciencesPhylogeneticsCATHECOLProteobacteriaBotanySoil PollutantsEnvironmental ChemistryPolycyclic Aromatic HydrocarbonsWaste Management and Disposal030304 developmental biology0303 health sciencesMultiple sequence alignmentBacteriabiologyPhylogenetic tree030306 microbiologybiology.organism_classification16S ribosomal RNAPollutionActinobacteriaBiodegradation EnvironmentalCoalPCR[SDE]Environmental SciencesHorizontal gene transferBIODIVERSITYRestriction fragment length polymorphismPrimer (molecular biology)CAT A SEQUENCEJournal of Hazardous Materials
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Micellar electrokinetic chromatography with bile salts for predicting ecotoxicity of aromatic compounds.

2004

The retention factors of several aromatic compounds were obtained by micellar electrokinetic chromatography (MEKC) using cholate, taurocholate, deoxycholate and deoxytaurocholate as micellar systems. The possibility of using these retention factors to describe and predict several ecotoxicological activities of different aromatic compounds was evaluated. Adequate correlations retention–ecotoxicity (log LC50 in fish and daphnia, log EC50 in green algae and daphnia, chronic values in fish and green algae, bioconcentration factor, and soil sorption coefficient) were obtained for the micellar systems studied. The predictive ability of the models obtained for these micellar systems was compared. …

Daphnia magnaPolycyclic aromatic hydrocarbonBioconcentrationmacromolecular substancesBiochemistryDaphniaMicellar electrokinetic chromatographyAnalytical ChemistryBile Acids and SaltsAnimalsPolycyclic CompoundsChromatography Micellar Electrokinetic Capillarychemistry.chemical_classificationChromatographybiologyOrganic ChemistryFishesGeneral MedicineReference Standardsbiology.organism_classificationHydrocarbonchemistryDaphniaEnvironmental chemistryGreen algaeIndicators and ReagentsEcotoxicityWater Pollutants ChemicalJournal of chromatography. A
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New micromethod combining miniaturized matrix solid-phase dispersion and in-tube in-valve solid-phase microextraction for estimating polycyclic aroma…

2008

Abstract Miniaturized matrix solid-phase dispersion (MSPD) was developed for the extraction of common polycyclic aromatic hydrocarbons (PAHs) from bivalve samples (100 mg, dry weight). Additional clean-up and analyte enrichment was accomplished by in-tube solid-phase microextraction (SPME). For this purpose the extracts collected after MSPD were diluted with water and injected into a capillary column coated with the extractive phase. This capillary column was connected to the analytical column by means of a switching valve. Separation and quantification of the PAHs were carried out using a monolithic LC column and fluorescence detection. Since the in-tube SPME device allowed the processing …

Detection limitAnalyteChromatographyChemistryOrganic ChemistryExtraction (chemistry)Analytical chemistryReproducibility of ResultsGeneral MedicineReference StandardsSolid-phase microextractionBiochemistryHigh-performance liquid chromatographySensitivity and SpecificityAnalytical ChemistryBivalviaMatrix (chemical analysis)AnimalsSample preparationSolid phase extractionPolycyclic Aromatic HydrocarbonsSolid Phase MicroextractionChromatography LiquidJournal of chromatography. A
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Analysis of Polycyclic Aromatic Hydrocarbons and Their Oxygen-Containing Derivatives and Metabolites in Soils

2010

Although polycyclic aromatic hydrocarbons (PAHs) have been extensively studied, the knowledge of their oxygen-containing derivatives and metabolites (OPAHs) in soils is limited. We modified and tested an existing analytical protocol involving pressurized liquid extraction of soil followed by fractionation of target compounds into PAHs and OPAHs on a silica gel column and gas chromatography/ mass spectrometry-based separation and quantification. Polycyclic aromatic hydrocarbons and carbonyl-OPAHs were quantified directly after separation on silica gel columns, and hydroxyl/carboxyl-OPAHs were quantified after silylation with N,O-bis(trimethylsilyl)trifluoroacetamide. Recoveries between 78 an…

Detection limitEnvironmental EngineeringChromatographyOpahbiologySilylationChemistrySilica gelExtraction (chemistry)Industrial WasteFractionationManagement Monitoring Policy and Lawbiology.organism_classificationPollutionOxygenSoilchemistry.chemical_compoundEnvironmental chemistrySoil PollutantsSample preparationGas chromatographyPolycyclic Aromatic HydrocarbonsWaste Management and DisposalEnvironmental MonitoringWater Science and TechnologyJournal of Environmental Quality
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Comparison of different methods for extraction of polycyclic aromatic hydrocarbons (PAHs) from Sicilian (Italy) coastal area sediments.

2012

This paper describes a work aimed at improving the conditions of an extraction method, coupling GC-MS determination, for the analysis without cleanup phase, of polycyclic aromatic hydrocarbons (PAHs) from sediment samples. The automatic Soxhlet extraction in warm mode (using Extraction System B-811 Standard, Buchi) has demonstrated advantages for automation, reduced extraction time, and lower solvent use than for conventional Soxhlet extraction. Under these conditions, the recoveries are very good as they resulted greater than 85 % and, in most of the cases, near 100 %. The repeatability is also satisfactory (relative standard deviation less than 15 %). The detection limits are also accepta…

Detection limitGeologic SedimentsExtraction (chemistry)SedimentGeneral MedicineRepeatabilityChemical FractionationManagement Monitoring Policy and LawPollutionGas Chromatography-Mass SpectrometrySettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliMatrix (chemical analysis)Dry weightEnvironmental chemistryEnvironmental scienceEcotoxicologySeawaterSettore CHIM/01 - Chimica AnaliticaPolycyclic Aromatic HydrocarbonsGas chromatography–mass spectrometryAutomatic extraction .CRM . PAHs . Sediments . GC-MSSicilyWater Pollutants ChemicalEnvironmental MonitoringGeneral Environmental Science
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