Search results for "Lethal Dose 50"

showing 10 items of 57 documents

Cuticular hydrocarbon profiles in Blattella germanica: effects of halofenozide, boric acid and benfuracarb

2006

1379-1176 (Print) Journal Article; In order to complete previous studies conducted on Blattella germanica, three insecticides from different groups were evaluated: boric acid, an inorganic compound, benfuracarb, a carbamate, and halofenozide, a non-steroidal ecdysone agonist. Boric acid (8.20%, LD50) and benfuracarb (2%, LD50) were incorporated into the diet and orally administrated to newly emerged adults of both sexes, while halofenozide (0.33%, LD50) was applied topically. Hydrocarbons extracts was made on bidistilled pentane from control and treated series sampled 6 days following treatment. Extracts was analyzed by gas chromatography. Data showed that cuticular profiles of control and …

OralMaleChromatographyHydrazines/*toxicityTime Factorsintegumentary systembeta-Alanine/*analogs & derivatives/toxicityHydrocarbons/*analysisBenzofurans/*toxicityBenzoic Acids/*toxicityLethal Dose 50TopicalInsecticides/*toxicityBoric Acids/*toxicityGasAdministrationAnimalsFemaleBlattellidae/chemistry/drug effects/growth & development
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Photoinduced toxicity of retene to Daphnia magna under enhanced UV-B radiation.

2001

Abstract The effects of UV radiation on the acute toxicity of retene (7-isopropyl-1-methylphenanthrene) to Daphnia magna Straus were studied. Dehydroabietic acid (DHAA) from which retene is formed in the vicinity of pulp and paper industry was also studied. Pyrene, anthracene, and phenanthrene were used as model PAH compounds. The time taken for immobilization (ET50) was monitored under biologically effective UV-B dose rates of 240, 365, 565, and 650 mW m−2 (UV-A and visible light also present). Median effective concentrations (EC50) were determined after a 15-min UV exposure (565 mW m−2) followed by 24 h in the dark. Retene ( 10–320 μg l −1 ) was not acutely toxic in the dark. The inductio…

PaperEnvironmental EngineeringPhotochemistryUltraviolet RaysHealth Toxicology and MutagenesisDaphnia magnaIndustrial WasteAbsorptionLethal Dose 50chemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryAnimalsPolycyclic Aromatic HydrocarbonsAnthraceneRetenebiologyPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPhenanthrenePhenanthrenesbiology.organism_classificationPollutionAcute toxicitychemistryDaphniaToxicityAbietanesPyreneDiterpenesPhototoxicityWater Pollutants ChemicalNuclear chemistryChemosphere
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Correlation of pharmacological properties of a group of beta-blocker agents by molecular topology.

1995

Abstract The molecular connectivity method has been applied to the study of pharmacological properties, among which are found the angor treatment dose, α-distribution half-life and intravenous LD50 in mouse, of a group of β-blocker agents, verifying its application in the prediction of theoretic values for said pharmacological properties. To do this, the obtained multiple regression functions of the corresponding connectivity indices were used in relation with the experimental values of the properties, which are accompanied by the statistical parameters used in their selection criteria, as well as the corresponding random and cross-validation studies of said functions, which corroborate the…

PharmacologyStereochemistryGroup (mathematics)Adrenergic beta-AntagonistsStatistical parameterPharmaceutical ScienceBiological activityCorrelationLethal Dose 50MiceRandom AllocationStructure-Activity RelationshipTreatment doseModels ChemicalLinear regressionInjections IntravenousAnimalsRegression AnalysisMolecular topologyBiological systemSoftwareMathematicsHalf-LifeThe Journal of pharmacy and pharmacology
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Acute toxicity and bioaccumulation of endosulfan in rotifer (Brachionus calyciflorus).

1991

Abstract 1. 1. The acute toxicity of endosulfan was determined for the freshwater rotifer Brachionus calyciflorus . 2. 2. The mean 24 hr lc 50 value for endosulfan was 5.15 ppm with a coefficient of variation of 14.7%. 3. 3. Rotifers were exposed at two sublethal concentrations (1.5–2.0 ppm) of endosulfan for bioaccumulation experiments, for an exposure time of 24, 48, 72 and 96 hr. The rotifers were fed with Nannochloris oculata (5 × 10 5 cell/ml). 4. 4. The highest accumulation of endosulfan was found 24 hr after the start of the exposure to 1.5 ppm of the toxicant. A steady-state concentration in rotifer was reached between 24–48 hr, followed by a gradual decrease until 96 hr.

PharmacologybiologyImmunologyRotiferaRotiferBrachionusbiology.organism_classificationAcute toxicityToxicologyLethal Dose 50chemistry.chemical_compoundAnimal sciencechemistryBioaccumulationToxicityBrachionus calyciflorusAnimalsEndosulfanEndosulfanWater Pollutants ChemicalToxicantComparative biochemistry and physiology. C, Comparative pharmacology and toxicology
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Temperature-toxicity relationships of fluvalinate (synthetic pyrethroid) on Procambarus clarkii (Girard) under laboratory conditions.

1988

Procambarus clarkiiInsecticidesPyrethroidHealth Toxicology and MutagenesisTemperatureFresh WaterGeneral MedicineAstacoideaBiologyToxicologybiology.organism_classificationPollutionToxicologyFluvalinateLethal Dose 50chemistry.chemical_compoundchemistryEnvironmental chemistryToxicityNitrilesPyrethrinsAnimalsNon target organismBulletin of environmental contamination and toxicology
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Cytotoxicity and antimitotic activity of Rhinella schneideri and Rhinella marina venoms.

2019

Abstract Ethnopharmacological relevance Rhinella schneideri and Rhinella marina are toad venoms distributed in different parts of the world, including Brazil, Columbia and amazon. Venoms extracted from different species have many clinical applications such as antimicrobial cardiotonics and treatment of cancer. Aim of the study; In this study, we aim to investigate the effect of venoms extracted from R. schneideri and R. marina on cancer cells and verify possible mechanism of action. Material and method Cytotoxicity analyses was performed using the resazurin reduction assay, where different concentrations of venoms were tested against sensitive CCRF-CEM and P-gp overexpressing ADR/CEM5000 le…

Programmed cell deathCell SurvivalAntimitotic AgentsLethal Dose 5003 medical and health scienceschemistry.chemical_compound0302 clinical medicineTubulinRhinella schneideriCell Line TumorDrug DiscoveryAnimalsHumansPropidium iodideCytotoxicity030304 developmental biologyPharmacology0303 health sciencesbiologyBufalinCell Cycle Checkpointsbiology.organism_classificationBufonidaeMolecular Docking SimulationTubulinchemistryBiochemistryApoptosis030220 oncology & carcinogenesisCancer cellbiology.proteinAmphibian VenomsJournal of ethnopharmacology
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Tumor cell specific toxicity of Inula helenium extracts.

2006

The aim of the research program was to identify botanical extracts with antineoplastic activity. In this respect extracts prepared from Inula helenium roots showed a remarkable activity. As evidenced by the MTT assay, the Inula helenium extract revealed a highly selective toxicity toward four different tumor cell lines (HT-29, MCF-7, Capan-2 and G1), but a much lower toxicity against healthy human peripheral blood lymphocytes (PBLs) from two donors. The extract-induced death of tumor cells was studied extensively by electron microscopy. There was a remarkable similarity of morphological alterations observed in the four cell lines: patchy chromatin condensations, cytoplasmic vesiculation, sw…

Programmed cell deathCell SurvivalContext (language use)Plant RootsLethal Dose 50Cell Line TumorToxicity Tests AcuteHumansMTT assayLymphocytesAnnexin A5CytotoxicityPharmacologyInulabiologyMutagenicity TestsPlant Extractsbiology.organism_classificationMolecular biologyAntineoplastic Agents PhytogenicApoptosisCell cultureImmunologyInulaHT29 CellsHeleniumPhytotherapy research : PTR
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Use of molecular topology for the prediction of physico-chemical, pharmacokinetic and toxicological properties of a group of antihistaminic drugs

2002

We used molecular connectivity to search mathematical models for predicting physico-chemical (e.g. the partition coefficient, P), pharmacokinetic (e.g. the time of maximum plasma level, and toxicological properties (lethal dose, LD) for a group of antihistaminic drugs. The results obtained clearly reveal the high efficiency of molecular topology for the prediction of these properties. Randomization and cross-validation by use of leave-one-out tests were also performed in order to assess the stability and the prediction ability of the connectivity functions selected.

Quantitative structure–activity relationshipChemistryQuantitative Structure-Activity RelationshipPharmaceutical SciencePlasma levelsPharmacologyModels BiologicalLethal Dose 50Structure-Activity RelationshipPharmacokineticsPredictive Value of TestsHistamine H1 AntagonistsRegression AnalysisAntihistaminic drugsMolecular topologyBiological systemInternational Journal of Pharmaceutics
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Pathogenicity of intrathoracically administrated Bacillus thuringiensis spores in Blatta orientalis.

2006

Abstract The ability of Bacillus thuringiensis to produce septicaemia in Periplaneta americana and Blatta orientalis has been investigated. Spores and crystals from several wild-type strains as well as spores of a B. thuringiensis crystal-deficient mutant, were first orally administrated at high doses, and no significant mortality was recorded. Intrathoracic injection of spore suspensions in P. americana revealed that this species is not very susceptible to B. thuringiensis spores. B. orientalis , by contrast, was found to be very susceptible to B. thuringiensis , with a LD 50 of about 35,000 spores, that is similar to that reported on Lepidoptera challenged with parenterally injected B. th…

Spores Bacterialanimal structuresbiologyVirulencefungiBlattaBacillus thuringiensisAdministration OralCockroachesThoraxbiology.organism_classificationMedian lethal doseBacillalesSporeMicrobiologyLepidoptera genitaliaLethal Dose 50BiopesticideBacillus thuringiensisAnimalsDisease SusceptibilityPest Control BiologicalEcology Evolution Behavior and SystematicsPeriplanetaJournal of invertebrate pathology
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Effect of polybrominated biphenyls on bromobenzene lethality in mice.

1977

Polybrominated biphenyls (PBBs) are inducers of hepatic microsomal cytochrome P450 and P1 450 in rats and mice. The purpose of this study was to determine, in mice, the effect of PBBs on the lethality of the hepatotoxin bromobenzene. Female NMRI mice were administered a single ip injection of 150 mg/kg PBBs and other mice received phenobarbital (PB), 100 mg/kg daily for 3 days, or 3‐methylcholanthrene (MC), 20 mg/kg daily for 3 days. At 24 hr after PB or MC and 24, 48, and 96 hr after PBBs animals received 3,150 mg/kg bromobenzene ip (LD85) and the time to death was recorded. Both PB and MC enhanced bromobenzene lethality and decreased the median time to death (LT50) from 23 hr in controls …

Time FactorsStereochemistryPolybrominated BiphenylsPharmacologyToxicologyLethal Dose 50chemistry.chemical_compoundMicemedicineAnimalsDrug InteractionsbiologyBiphenyl CompoundsHepatotoxinCytochrome P450PollutionGlutathionechemistryLiverBromobenzeneNmri micePhenobarbitalMicrosomebiology.proteinLethalityPhenobarbitalPolybrominated BiphenylsFemalemedicine.drugBromobenzenesMethylcholanthreneJournal of toxicology and environmental health
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