Search results for "Toxicity tests"

showing 10 items of 141 documents

Toxicological interactions between the mycotoxins beauvericin, deoxynivalenol and T-2 toxin in CHO-K1 cells in vitro.

2011

Abstract Beauvericin (BEA), deoxynivalenol (DON) and T-2 toxin (T-2) are important food-borne mycotoxins that have been implicated in human health. In this study, the acute toxicity of individual and combined mycotoxins (BEA, DON and T-2) were tested in immortalized hamster ovarian cells (CHO-K1) at 24, 48 and 72 h of exposure, by the tetrazolium salt (MTT) and neutral red (NR) assays. The IC50 values obtained for all mycotoxins by the MTT and NR assays ranged from 0.017 to 12.08 μM and from 0.042 to 17.22 μM, respectively. Both, individual and combined mycotoxins demonstrated a significant cytotoxic effect in CHO-K1 cells in a dose-dependent manner. When mycotoxins were assayed individuall…

Neutral redToxinHamsterCHO CellsPharmacologyToxicologymedicine.disease_causeAcute toxicityBeauvericinToxicologychemistry.chemical_compoundInhibitory Concentration 50T-2 ToxinchemistryCricetinaeDepsipeptidesmedicineToxicity Tests AcuteAnimalsAntagonismCytotoxicityMycotoxinTrichothecenesToxicon : official journal of the International Society on Toxinology
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Caloric content of Daphnia magna as reflect of propanil stress during a short-term exposure and its relationship to long-term responses

2013

The present study investigates energy stores changes in the aquatic invertebrate Daphnia magna following a 5-d exposure to propanil. Juveniles of D. magna were exposed to sublethal propanil concentrations (0.07, 0.10, 0.21 and 0.55 mgl(-1)) which were used previously to test their effect on reproduction, growth and survival (21 days test) of D. magna. Glycogen, total lipids, proteins, and dry weight were determined in control and exposed daphnids at 24, 48, 72, 96 and 120 h. Data were used to calculate caloric content as biomarker of propanil exposure. Results showed a depletion of energy reserves in D. magna exposed to the herbicide. At 120 h of exposure to the highest propanil concentrati…

OffspringHealth Toxicology and Mutagenesismedia_common.quotation_subjectDaphnia magnaPropanilToxicologyDaphniaArthropod ProteinsToxicologychemistry.chemical_compoundAnimal scienceDry weightToxicity TestsPropanilAnimalsmedia_commonPharmacologyGlycogenbiologyHerbicidesLipid metabolismGeneral MedicineLipid Metabolismbiology.organism_classificationDaphniachemistryReproductionGlycogenWater Pollutants ChemicalEnvironmental Toxicology and Pharmacology
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Experimental techniques for testing the sensitivity of bladder tumours to antineoplastic drugs

1973

A number of laboratory tests can be employed to examine the sensitivity of human bladder tumour cells to various chemotherapeutic agents.-Their principles and methods, and some preliminary results, are described with special reference to certain in vitro and in vivo cytotoxicity tests and to heterotransplantation in the hamster. Satisfactory agreement has sometimes been observed between experimental results and clinical responses, but our experience is still very limited.-The employment of several such tests would probably lead to a greater degree of reliability in the laboratory assessment of the sensitivity of bladder tumours to cytotoxic drugs.

Oncologymedicine.medical_specialtyPathologyAdministration TopicalUrologyTransplantation HeterologousHuman bladderDrug ResistanceHamsterAntineoplastic AgentsBLADDER PAPILLOMAThiophenesFluorescenceCricetinaeInternal medicinemedicineAnimalsHumansGlycosidesMelphalanIn vivo cytotoxicityPodophyllotoxinCell NucleusCarcinoma Transitional Cellbusiness.industryDaunorubicinDemecolcineDNA NeoplasmCytotoxicity Tests ImmunologicMicroscopy FluorescenceUrinary Bladder NeoplasmsDoxorubicinProtein BiosynthesisAntineoplastic DrugsOxidoreductasesbusinessNeoplasm TransplantationThiotepaUrological Research
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Dynamic regulation of CD8 T cell tolerance induction by liver sinusoidal endothelial cells.

2010

Abstract Cross-presentation of soluble Ag on MHC class I molecules to naive CD8 T cells by liver sinusoidal endothelial cells (LSECs) leads to induction of T cell tolerance that requires interaction between coinhibitory B7-H1 on LSECs and programmed cell death-1 on CD8 T cells. In this study, we investigate whether cross-presentation of high as well as low Ag concentrations allowed for LSEC-induced tolerance. Ag concentration directly correlated with the cross-presentation capacity of murine LSECs and thus strength of TCR stimulation. Although LSEC cross-presentation at low-Ag concentrations resulted in tolerance, they induced differentiation into effector T cells (CTL) at high-Ag concentra…

OvalbuminT cellImmunologychemical and pharmacologic phenomenaMice TransgenicCD8-Positive T-LymphocytesLymphocyte ActivationResting Phase Cell CycleMiceCross-PrimingAntigenMHC class ImedicineImmune ToleranceImmunology and AllergyCytotoxic T cellAnimalsCells CulturedMice KnockoutAntigen PresentationbiologyT-cell receptorEndothelial CellsCytotoxicity Tests ImmunologicCoculture TechniquesCell biologyMice Inbred C57BLTolerance inductionCTL*medicine.anatomical_structureLiverbiology.proteinCD80Journal of immunology (Baltimore, Md. : 1950)
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Test procedures for obtaining representative extracts suitable for reliable in vitro toxicity assessment of paper and board intended for food contact.

2009

International audience; This paper describes the use of a suite of extraction procedures applicable to the assessment of the in vitro toxicity of paper/board samples intended for food-contact applications. The sample is extracted with ethanol, water, or exposed to modified polyphenylene oxide (Tenax) for fatty, non-fatty and dry food applications, respectively. The water extracts are directly suitable for safety assessment using in vitro bioassays. The ethanol extracts of the paper/board and of the exposed Tenax require pre-concentration to give acceptable sensitivity. This is because the in vitro bioassays can tolerate only a small percentage of added organic solvent before the solvent its…

PaperFood contact materialsHealth Toxicology and MutagenesisSample (material)[ SDV.TOX ] Life Sciences [q-bio]/ToxicologyTenax[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainIn Vitro TechniquesToxicologyPaper and boardMESH : Gas Chromatography-Mass Spectrometry01 natural sciencesMESH : Food PackagingGas Chromatography-Mass SpectrometryMESH : Toxicity Tests0404 agricultural biotechnologyToxicity TestsBioassayPaperboardMESH : WoodFood contactbusiness.industryTest procedures010401 analytical chemistryExtraction (chemistry)Food PackagingPublic Health Environmental and Occupational HealthLife Sciences04 agricultural and veterinary sciencesGeneral ChemistryGeneral MedicinePulp and paper industryToxicity assessmentWood040401 food science0104 chemical sciencesBiotechnologyMESH : PaperIn vitro testingExtraction proceduresFood contact materialsvisual_artvisual_art.visual_art_mediumEnvironmental sciencebusinessFood Science
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The BIOSAFEPAPER project for in vitro toxicity assessments: preparation, detailed chemical characterisation and testing of extracts from paper and bo…

2008

International audience; Nineteen food contact papers and boards and one non-food contact board were extracted following test protocols developed within European Union funded project BIOSAFEPAPER. The extraction media were either hot or cold water, 95% ethanol or Tenax, according to the end use of the sample. The extractable dry matter content of the samples varied from 1200 to 11,800 mg/kg (0.8-35.5 mg/dm2). According to GC-MS the main substances extracted into water were pulp-derived natural products such as fatty acids, resin acids, natural wood sterols and alkanols. Substances extracted into ethanol particularly, were diisopropylnaphthalenes, alkanes and phthalic acid esters. The non-foo…

PaperPolymersCytotoxicityTenaxFood Contamination[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainToxicologymedicine.disease_causeRisk Assessment01 natural sciencesGas Chromatography-Mass Spectrometrychemistry.chemical_compound0404 agricultural biotechnologyBacillus cereusToxicity TestsmedicineAnimalsHumansBioassaymedia_common.cataloged_instanceChemical analysisEuropean unionmedia_commonChromatographyEthanolMutagenicity TestsFatty Acids010401 analytical chemistryFood PackagingWaterEnvironmental Exposure04 agricultural and veterinary sciencesGeneral MedicineBSTFA040401 food science0104 chemical sciencesSterolsPhthalic acidchemistryGlobal bioassayBIOSAFEPAPERToxicityBiological AssaySafetyGas chromatography–mass spectrometryGenotoxicityFood Science
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Biological effects of high molecular weight lignin derivatives

2010

Abstract A number of high molecular weight (HMW) lignin derivatives possessing varied chemical properties were screened for their biological effects in order to obtain more information on the possible structural features of HMW lignin-related effects. The studied compounds were both commercial and in-house extracted lignin derivatives. Bioassays used include reverse electron transport (RET), Vibrio fischeri, Daphnia magna , and juvenile rainbow trout ( Oncorhynchus mykiss) hepatocytes. The studied lignin derivatives inhibited the in vitro systems and luminescence of V. fischeri bacteria to some extent–daphnids were not affected. It seems that, at least in the RET assay, certain pH-dependent…

Paperendocrine systemHealth Toxicology and MutagenesisDaphnia magnaLigninWaste Disposal Fluidcomplex mixturesMicrobiologyElectron Transportchemistry.chemical_compoundToxicity TestsCytochrome P-450 CYP1A1AnimalsLigninBioassayFinlandVibriobiologyfungitechnology industry and agriculturePublic Health Environmental and Occupational Healthfood and beveragesBiological activityGeneral Medicinebiology.organism_classificationPollutionIn vitroVibrioReverse electron flowDaphniachemistryBiochemistryOncorhynchus mykissHepatocytesBiological AssayWater Pollutants ChemicalBacteriaEcotoxicology and Environmental Safety
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An in vitro procedure for evaluation of early stage oxidative stress in an established fish cell line applied to investigation of PHAH and pesticide …

2004

Oxidative stress by increased production of reactive oxygen species such as superoxide has been implicated in the toxicity of PCB's and non-target toxicity of many pesticides. We report the development of a microplate-based method for determination of early stage oxidative stress using an established cell line (EPC) from a skin tumour of carp Cyprinus carpio L. and 2',7'-dichlorodihydrofluorescein diacetate (H(2)-DCFDA) as a fluorescent probe for detection of reactive oxygen species (ROS) formation. Sublethal concentrations of the herbicide Paraquat, an established redox cycling agent and a crude PCB mixture, Arochlor 1254 elicited a linear increase in ROS formation over 2 h exposure which …

ParaquatAroclorsCarpsTime FactorsAquatic ScienceBiologyIn Vitro TechniquesOceanographymedicine.disease_causePesticide toxicityToxicologychemistry.chemical_compoundParaquatToxicity TestsmedicineTumor Cells CulturedAnimalsPesticidesFluorescent Dyeschemistry.chemical_classificationReactive oxygen speciesSuperoxideGeneral MedicineFluoresceinsPollutionpeople.cause_of_deathAcute toxicityOxidative StresschemistryBiochemistryToxicityMalathionpeopleReactive Oxygen SpeciesOxidative stressMarine environmental research
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Refining in vitro neurotoxicity testing--the development of blood-brain barrier models.

2003

The purpose of this paper is to review the current state of development of advanced in vitro blood–brain barrier (BBB) models. The BBB is a special capillary bed that separates the blood from the central nervous system (CNS) parenchyma. Astrocytes maintain the integrity of the BBB, and, without astrocytic contacts, isolated brain capillary endothelial cells in culture lose their barrier characteristics. Therefore, when developing in vitro BBB models, it is important to add astrocytic factors into the culture system. Recently, novel filter techniques and co-culture methods have made it possible to develop models which resemble the in vivo functions of the BBB in an effective way. With a BBB…

Pathologymedicine.medical_specialtyIn Vitro TechniquesBiologyIn Vitro TechniquesToxicologyBlood–brain barrierModels BiologicalGeneral Biochemistry Genetics and Molecular BiologyIn vivoToxicity TestsmedicinePharmacokineticsCells CulturedNeurotoxicityEndothelial CellsGeneral MedicineIsolated brainmedicine.diseaseCell biologyEndothelial stem cellMedical Laboratory Technologymedicine.anatomical_structurenervous systemBlood-Brain BarrierAstrocytescardiovascular systemNeuronAstrocyteAlternatives to laboratory animals : ATLA
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Adhesion prophylaxis using a copolymer with rationally designed material properties.

2008

Physical barriers are the only licensed adjuncts for adhesion prophylaxis in the United States and Europe. Here, we investigate D,L-polylactide-epsilon-caprolactonetrimethylenecarbonate (PCT copolymer), which is a rationally designed biomaterial, as an adhesion barrier.PCT copolymer membranes were produced by polymerization of the monomers, dissolution in organic solvents, and subsequently processing them by means of modified phase inversion and freeze drying. In vitro cytotoxicity was assayed by fibroblast culture. In vivo adhesion prophylaxis was studied in a rat model that involved standardized traumatization by electrocautery and suturing. The quantity and quality of the resulting adhes…

Pathologymedicine.medical_specialtyPolyestersBiocompatible MaterialsTissue AdhesionsFreeze-dryingSerous MembraneIn vivoMaterials TestingToxicity TestsCopolymermedicineAnimalsHumansRats WistarCells Culturedbusiness.industryBiomaterialMembranes ArtificialAdhesionAdhesion barrierIn vitroRatsMembraneWounds and InjuriesSurgeryLaparoscopybusinessBiomedical engineeringSurgery
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