Search results for "Acute Toxicity"

showing 10 items of 96 documents

Acute toxicity of several pesticides to rotifer (Brachionus calyciflorus).

1992

biologyHealth Toxicology and MutagenesisRotiferaRotiferGeneral MedicinePesticideToxicologybiology.organism_classificationPollutionMedian lethal doseAcute toxicityToxicologyLethal Dose 50chemistry.chemical_compoundchemistryToxicityBrachionus calyciflorusMalathionAnimalsPesticidesEndosulfanBulletin of environmental contamination and toxicology
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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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Screening of physical–chemical methods for removal of organic material, nitrogen and toxicity from low strength landfill leachates

2002

Physical-chemical methods have been suggested for the treatment of low strength municipal landfill leachates. Therefore, applicability of nanofiltration and air stripping were screened in laboratory-scale for the removal of organic matter, ammonia, and toxicity from low strength leachates (NH4-N 74-220 mg/l, chemical oxygen demand (COD) 190-920 mg O2/l, EC50 = 2-17% for Raphidocelis subcapitata). Ozonation was studied as well, but with the emphasis on enhancing biodegradability of leachates. Nanofiltration (25 degrees C) removed 52-66% of COD and 27-50% of ammonia, the latter indicating that ammonia may in part have been present as ammonium salt complexes. Biological pretreatment enhanced t…

Environmental EngineeringChemical PhenomenaNitrogenHealth Toxicology and MutagenesisDaphnia magnaWater Purificationchemistry.chemical_compoundAmmoniaOxidants PhotochemicalOzoneRaphidocelis subcapitataAmmoniaToxicity TestsAnimalsSoil PollutantsEnvironmental ChemistryWater PollutantsAmmoniumAir strippingLeachateOrganic ChemicalsbiologyChemistry PhysicalChemical oxygen demandPublic Health Environmental and Occupational HealthGeneral MedicineGeneral Chemistrybiology.organism_classificationPollutionAcute toxicityRefuse DisposalOxygenDaphniachemistryEnvironmental chemistryFiltrationChemosphere
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Antipoxvirus Activity Evaluation of Optimized Corroles Based on Development of Autofluorescent ANCHOR Myxoma Virus

2021

International audience; A series of 43 antiviral corrole-based molecules have been tested on myxoma virus (Lausanne-like T1MYXV strain). An autofluorescent MYXV, with an ANCHOR cassette, has been used for the studies. A(2)B-fluorocorroles display various toxicities, from 40 being very toxic (CC50 = 1.7 mu M) to nontoxic 38 (CC50 > 50 mu M), whereas A(3)-fluorocorroles, with one to three fluorine atoms, are not toxic (with the exception of corroles 9, 10, and 22). In vitro, these compounds show a good selectivity index when used alone. Corrole 35 seems to be the most promising compound, which displays a high selectivity index with the lowest IC50. Interestingly, this "Hit" corrole is easy to…

0301 basic medicinePorphyrins[SDV]Life Sciences [q-bio]030106 microbiologyresistant strainMyxoma virusAntiviral Agents03 medical and health scienceschemistry.chemical_compoundmyxoma viruscorroleIn vivoAnimalsCorroleIC50Strain (chemistry)biologybiology.organism_classificationantiviralAcute toxicityIn vitro3. Good healthdsDNA virus030104 developmental biologyInfectious DiseaseschemistryBiochemistrypoxvirusRabbitsSelectivity
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A screening study on the fate of fullerenes (nC60) and their toxic implications in natural freshwaters

2013

Increasing usage of fullerenes (C60) increases their opportunities to be released into the environment. For risk assessment, it is important to understand the environmental fate and ecotoxicological effects of C60. In the present study, fullerene settling was measured during a 1-yr period with 4 different lake waters and an artificial freshwater, and Daphnia magna immobilization and fullerene accumulation was also measured in each of the lake waters. Depending on the characteristics of the lake waters, fullerenes either exhibited extended water stability or settled rapidly; in all waters, there was a fraction that remained stable after 1 yr. Water stability was affected by the quality and m…

FullerenebiologyChemistryHealth Toxicology and MutagenesisDaphnia magnabiology.organism_classificationAcute toxicityNatural organic matterSettlingMolecular sizeNanotoxicologyEnvironmental chemistryEnvironmental ChemistryScreening studyEnvironmental Toxicology and Chemistry
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An approach to the diazinon toxicity in the European eel: bioaccumulation studies

1993

Abstract The acute toxicity effects of diazinon on European eel ( Anguilla anguilla ) were examined using short-term exposures in static conditions. In these conditions the 96-h median lethal concentration (LC 50 ) was 0.086 mg/1. In addition, the eels were exposed to two sublethal diazinon concentrations, 0.042 and 0.056 mg/1 (1/2 and 2/3 LC 50 96-h, respectively) for different exposure times, till a maximum of 96 h, and bioaccumulation and clearance of this insecticide in liver, muscle, gill and blood tissues were studied. BCF values of diazinon after 96 h exposure to 0.042 mg/l were 1850 in liver, 875 in gill and 775 in eel muscle. BCF values of diazinon over a 48-h exposure period to 0.…

Gillanimal structuresEnvironmental EngineeringDiazinonbiologyPesticidebiology.organism_classificationPollutionAcute toxicityExcretionToxicologychemistry.chemical_compoundAnimal sciencechemistryAnguillidaeBioaccumulationToxicityEnvironmental ChemistryWaste Management and DisposalScience of The Total Environment
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Effect of potential antidotes on the acute toxicity of acrylonitrile

1981

Rats were intoxicated with lethal doses of acrylonitrile by different routes of application, and the effect of potential antidotes was studied. The cyanide antidotes 4-dimethylaminophenol plus thiosulfate showed some protective effect only after oral but not after i.p. or inhalatory acrylonitrile application. Of the sulfhydryl compounds cysteine, N-acetylcysteine, cysteamine and diethyldithiocarbamate the two antidotes cysteine and, to some lesser extent, N-acetylcysteine proved especially effective. Cysteine, at a dose of 200 mg/kg (i.p.), prevented the lethal effect of 100 mg/kg acrylonitrile (i.p.) even when given 2 h after the acrylonitrile dose. From these experiments a tentative sched…

Thiosulfatemedicine.medical_treatmentPublic Health Environmental and Occupational HealthPharmacologyAcute toxicitychemistry.chemical_compoundchemistrymedicineOrganic chemistryCysteamineAcrylonitrileAntidoteCysteineCYANIDE ANTIDOTESInternational Archives of Occupational and Environmental Health
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Cardiotoxicity and Cardioprotection by Artesunate in Larval Zebrafish

2019

Although artesunate (ART) is generally accepted as a safe and well-tolerated first-line treatment of severe malaria, cases of severe side effects and toxicity of this compound are also documented. This study applied larval zebrafishes to determine the acute toxicity and efficacy of ART and performed RNA-sequencing analyses to unravel the underlying signaling pathways contributing to ART’s activities. Results from acute toxicity assay showed that a single-dose intravenous injection of ART from 3.6 ng/fish (1/9 maximum nonlethal concentration) to 41.8 ng/fish (lethal dose 10%) obviously induced pericardial edema, circulation defects, yolk sac absorption delay, renal edema, and swim bladder l…

0301 basic medicinenatural productsHealth Toxicology and MutagenesisShort ReportmalariaDevelopmental toxicityPharmacologyToxicologyNephrotoxicity03 medical and health scienceschemistry.chemical_compound0302 clinical medicineEdemamedicinecancernetwork pharmacologyCardiotoxicityChemical Health and Safetybusiness.industrylcsh:RM1-950Public Health Environmental and Occupational Healthmedicine.diseaseAcute toxicity030104 developmental biologylcsh:Therapeutics. PharmacologychemistryArtesunate030220 oncology & carcinogenesisHeart failureToxicitymedicine.symptombusinessDose-Response
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Pharmacological evaluation of the dichloromethanol extract fromInula crithmoides L.

1995

The pharmacological effect of the dichloromethanol extract of Inula crithmoides L. was analysed in in vitro and in vivo models. The extract dose-dependently decreased arterial blood pressure and furthermore it showed low acute toxicity, CNS depressor activity and analgesic and antiinflammatory effects. Preincubation of the guinea-pig ileum and rat duodenum (100 μg/mL) produced a significant reduction in the contractile effects of histamine and acetylcholine and a concentration-related inhibition of the effects of serotonin. Following further fractionation the methylene chloride/acetone (50/50) fraction caused a significant decrease in motor activity and significantly reduced the threshold o…

PharmacologyInulabiologyAnalgesicBiological activityPharmacologybiology.organism_classificationAcute toxicitychemistry.chemical_compoundchemistryIn vivoAnesthesiaToxicitymedicineHistamineAcetylcholinemedicine.drugPhytotherapy Research
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ChemInform Abstract: Synthesis and Pharmacological Evaluation of 1-Methyl-5- [substituted-4(3H)-oxo-1,2,3-benzotriazin-3-yl]-1H-pyrazole-4-acetic Aci…

2010

Abstract Several new 1-methyl-5-[substituted-4-oxo-1,2,3-benzotriazin-3-yl]-1H-pyrazole-4-acetic acids and their ethyl ester derivatives were prepared. The compounds were tested for analgesic and antiinflammatory activities, acute toxicity, ulcerogenic effect, and as in vitro inhibitors of 3α-hydroxysteroid dehydrogenase (3α-HSD), since it is claimed that the inhibition of such an enzyme predicts in vivo antiinflammatory activity. Some compounds were more active than phenylbutazone in the phenylbenzoquinone and acetic acid peritonitis tests, and equiactive to the same drug in the carrageenin paw edema test. All the compounds inhibited the 3α-HSD, but no correlation was observed with the paw…

chemistry.chemical_classificationChemistryDehydrogenaseGeneral MedicinePyrazoleMedicinal chemistryAcute toxicityIn vitroAcetic acidchemistry.chemical_compoundEnzymeIn vivoPhenylbutazonemedicinemedicine.drugChemInform
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