Search results for "Viability assay"

showing 10 items of 279 documents

Lipid nanocarriers containing esters prodrugs of Flurbiprofen. Preparation, physical-chemical characterization and biological studies.

2013

In this paper, the preparation, chemical-physical, technological and in vitro characterization of nanostructured lipid carriers (NLC) carrying R-flurbiprofen ester prodrugs, were analyzed for a potential pharmaceutical application. R-flurbiprofen was chosen as a model drug because it has been found to play an effective role in counteracting secretases involved in neurodegenerative diseases, although it does not cross the Blood Brain Barrier (BBB). In this study, two R-flurbiprofen ester prodrugs (ethyl and hexyl) were successfully synthesized and entrapped into non-pegylated and pegylated NLC. The obtained systems showed average diameters in the colloidal size range, negative zeta potential…

Nanostructured Lipid CarriersMaterials scienceMagnetic Resonance SpectroscopyR-Flurbiprofen Ester ProdrugCell SurvivalFlurbiprofenStatic ElectricityBiomedical EngineeringPharmaceutical ScienceMedicine (miscellaneous)BioengineeringEsteraseBrain TargetingCell Line TumormedicineZeta potentialHumansGeneral Materials ScienceProdrugsViability assayParticle SizeCytotoxicityCell ShapeDrug CarriersNanostructured Lipid CarrierChromatographyDose-Response Relationship DrugEstersProdrugR-Flurbiprofen Ester ProdrugsLipidsIn vitroNanostructuresCitotoxicity Assays.BiochemistryFlurbiprofenSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryCitotoxicity AssaysDrug Deliverymedicine.drug
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T-2 toxin and its metabolites: Characterization, cytotoxic mechanisms and adaptive cellular response in human hepatocarcinoma (HepG2) cells

2020

Abstract The T-2 toxin (T-2) is a type A trichothecene produced by Fusarium species, and the most cytotoxic mycotoxin of the group. A study was made to determine T-2 cytotoxicity in human hepatocarcinoma (HepG2) cells; evaluate whether there is an adaptive response of HepG2 cells exposed to low concentrations of T-2; identify the T-2 metabolites by LC-Q-TOF MS; and determine whether T-2 disrupts cell proliferation in HepG2 cells. The IC50 values obtained ranged from 61.9 ± 2.4 nM to 70.7 ± 7.4 nM. No adaptive response was observed. There was no evidence of extra- or intracellular accumulation of T-2 after 24 h of exposure as determined by LC-Q-TOF MS. However, some T-2 metabolites such as H…

NecrosisCell SurvivalApoptosisToxicologymedicine.disease_causeNecrosis03 medical and health sciences0404 agricultural biotechnologymedicineHumansCytotoxic T cellViability assayCytotoxicity030304 developmental biology0303 health sciencesCell growthChemistryToxinCell CycleHep G2 Cells04 agricultural and veterinary sciencesGeneral MedicineAdaptation Physiological040401 food scienceMolecular biologyT-2 ToxinApoptosismedicine.symptomIntracellularFood ScienceFood and Chemical Toxicology
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Apoptotic activity of isoespintanol derivatives in human polymorphonuclear cells

2016

Background: Inflammation is a complex physiopathologic response to different stimuli. Recently, some pharmacological strategies have been proposed that could be used for resolution of inflammation by enhancing apoptosis of inflammatory cells. Objectives: To study in vitro apoptotic activity of isoespintanol [ISO] and of two semi-synthetic derivatives, bromide isoespintanol [BrI] and demethylated isoespintanol [DMI], in human polymorphonuclear (PMN) cells. Methods: PMN were exposed to the different concentrations of ISO, BrI and DMI for 30 min in phosphate-buffered saline pH 7.4 containing 1 mg/mL glucose, 0.4 mM Mg2+, and 1.20 mM Ca2+. Viability was assessed by dimethylthiazol diphenyl tetr…

NeutrófilosProgrammed cell deathNeutrophilsPopulationApoptosisBiologyApplied Microbiology and BiotechnologyFood processing and manufactureFlow cytometrychemistry.chemical_compoundneutrophilsAnnexinmedicineMTT assayPropidium iodideViability assayeducationPharmacology Toxicology and Pharmaceutics (miscellaneous)Pharmaceutical industryInflammationeducation.field_of_studyInflamaciónmedicine.diagnostic_testapoptosisTP368-456Molecular biologyIsoespintanolchemistryBiochemistryinflammationApoptosisCiencias MédicasHD9665-9675Food ScienceRevista Vitae
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Influence of E-smoking liquids on human periodontal ligament fibroblasts.

2014

Introduction: Over the last years, electronic cigarettes (ECs) have become more popular, particularly in individuals who want to give up smoking tobacco. The aim of the present study was to assess the influence of the different e-smoking liquids on the viability and proliferation of human periodontal ligament fibroblasts. Method and materials: For this study six test solutions with components from ECs were selected: lime-, hazelnut- and menthol-flavored liquids, nicotine, propylene glycol, and PBS as control group. The fibroblasts were incubated up to 96 h with the different liquids, and cell viability was measured by using the PrestoBlue® reagent, the ATP detection and the migration assay.…

NicotineCell SurvivalPeriodontal LigamentCellClinical NeurologyDentistryElectronic Nicotine Delivery SystemsAndrologyNicotinechemistry.chemical_compoundIn vitromedicinePeriodontal fiberHumansddc:610Viability assayGeneral DentistryIncubationCells CulturedCell proliferationMigration AssayDentistry(all)business.industryCell growthResearchSmokingFibroblastsMentholmedicine.anatomical_structureOtorhinolaryngologychemistryElectronic cigarettesNeurology (clinical)businessMentholmedicine.drugHeadface medicine
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Electrochemical sensor based on rGO/Au nanoparticles for monitoring H2O2 released by human macrophages

2021

Abstract Increased oxidative burden contributes to the pathogenesis of most inflammatory diseases and is associated with aging and chronic inflammation. Macrophages contribute to the generation of reactive oxygen species (ROS) within inflamed tissues. Currently, ROS generation is measured using fluorescent probes and colorimetric/fluorimetric biochemical assays. Hydrogen peroxide (H2O2) diffuses through the cell membrane and can be monitored in the extracellular space. Herein, we present a sensor for H2O2 detection released by cells in culture supernatants. H2O2 sensing performance was evaluated using chronoamperometric detection. A sensitivity of 0.0641 μA μM−1 cm−2 with a limit of detecti…

Nigericin02 engineering and technology010402 general chemistrymedicine.disease_cause01 natural sciencesFlow cytometrychemistry.chemical_compoundSettore ING-IND/17 - Impianti Industriali MeccaniciMaterials ChemistrymedicineExtracellularGold nanoparticlesViability assayElectrical and Electronic EngineeringInstrumentationGraphene oxidechemistry.chemical_classificationReactive oxygen speciesmedicine.diagnostic_testMacrophagesMetals and Alloys021001 nanoscience & nanotechnologyCondensed Matter PhysicsHydrogen peroxide0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSettore ING-IND/23 - Chimica Fisica ApplicatachemistryElectrochemical sensorCell cultureOxidative stressBiophysics0210 nano-technologyOxidative stressIntracellular
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Neurotoxic effects of ochratoxin A on the subventricular zone of adult mouse brain

2014

Ochratoxin A (OTA), a mycotoxin that was discovered as a secondary metabolite of the fungal species Aspergillus and Penicillium, is a common contaminant in food and animal feed. This mycotoxin has been described as teratogenic, carcinogenic, genotoxic, immunotoxic and has been proven a potent neurotoxin. Other authors have previously reported the effects of OTA in different structures of the central nervous system as well as in some neurogenic regions. However, the impact of OTA exposure in the subventricular zone (SVZ) has not been assessed yet. To elucidate whether OTA affects neural precursors of the mouse SVZ we investigated, in vitro and in vivo, the effects of OTA exposure on the SVZ …

Ochratoxin Aanimal diseasesCellular differentiationSubventricular zoneAnatomyBiologyToxicologyNeural stem cellCell biologychemistry.chemical_compoundmedicine.anatomical_structurenervous systemNeuroblastchemistryIn vivomedicineNeurotoxinViability assayJournal of Applied Toxicology
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Cytotoxic effect of silorane and methacrylate based composites on the human dental pulp stem cells and fibroblasts

2014

Objectives: The aim of this study was to compare the cytotoxic effect of a methacrylate-based and a silorane- based composite on the human dental pulp stem cells (DPSCs) versus human dental pulp fibroblasts (DPFs). Study Design: Samples of the Filtek Z250 and P90 were polymerized and immersed in the culture medium to obtain extracts after incubation for one, seven and 14 days. Magnetic cell sorting based on the CD146 expression was performed to purify DPSCs and DPFs. After incubation of both cells with the extracts, cytotoxicity was de - termined using the MTT test. Results: For the extracts of first and seventh day, both composites showed significantly lower cytotoxicity on DPSCs than DPFs…

OdontologíaComposite Resinsstomatognathic systemDental pulp stem cellsCytotoxic T cellHumansViability assaySilorane ResinsComposite materialCytotoxicityGeneral DentistryIncubationDental PulpOral Medicine and PathologyChemistryResearchStem CellsFibroblasts:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASPulp (tooth)MethacrylatesSurgeryStem cellSilorane ResinsMedicina Oral, Patología Oral y Cirugía Bucal
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Bcl-xL and Myeloid cell leukaemia-1 contribute to apoptosis resistance of colorectal cancer cells

2008

AIM: To explore the role of Bcl-x(L) and Myeloid cell leukaemia (Mcl)-1 for the apoptosis resistance of colorectal carcinoma (CRC) cells towards current treatment modalities. METHODS: Bcl-x(L) and Mcl-1 mRNA and protein expression were analyzed in CRC cell lines as well as human CRC tissue by Western blot, quantitative PCR and immunohistochemistry. Bcl-x(L) and Mcl-1 protein expression was knocked down or increased in CRC cell lines by applying specific siRNAs or expression plasmids, respectively. After modulation of protein expression, CRC cells were treated with chemotherapeutic agents, an antagonistic epidermal growth factor receptor (EGFR1) antibody, an EGFR1 tyrosine kinase inhibitor, …

Organoplatinum CompoundsCell SurvivalCellbcl-X ProteinAntineoplastic AgentsApoptosisBcl-xLAdenocarcinomaBiologyIrinotecanTNF-Related Apoptosis-Inducing LigandDownregulation and upregulationhemic and lymphatic diseasesCell Line TumormedicineHumansRNA Messengerfas ReceptorViability assayneoplasmsColorectal CancerGastroenterologyGeneral MedicineTransfectionFas receptorMolecular biologydigestive system diseasesErbB ReceptorsOxaliplatinmedicine.anatomical_structureProto-Oncogene Proteins c-bcl-2ApoptosisCell cultureCancer researchbiology.proteinMyeloid Cell Leukemia Sequence 1 ProteinCamptothecinFluorouracilColorectal NeoplasmsWorld Journal of Gastroenterology
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Effects of a low-level diode laser on oral keratinocytes, oral fibroblasts, endothelial cells and osteoblasts incubated with bisphosphonates: An

2014

Bisphosphonate-associated osteonecrosis of the jaw may have multiple causes, including altered bone remodeling, angiogenesis inhibition and impact of bisphosphonate on the soft tissues. Successful treatment is difficult. As a positive effect of low-level laser application on wound healing is well known, an in vitro study was designed to analyze the effect of low-level laser (280 mW, 670 nm) treatment on keratinocytes, fibroblasts, endothelial cells and osteoblasts treated with clodronate, ibandronate, pamidronate or zoledronate. Pure irradiation had a positive effect on cell viability, whereas bisphosphonate treatment had a negative impact. Viability was significantly increased in cells tre…

Pathologymedicine.medical_specialtyBisphosphonate-associated osteonecrosis of the jawbusiness.industryGeneral Neurosciencemedicine.medical_treatmentCellGeneral MedicineArticlesBisphosphonatemedicine.diseaseGeneral Biochemistry Genetics and Molecular BiologyBone remodelingmedicine.anatomical_structureApoptosismedicineCancer researchViability assayGeneral Pharmacology Toxicology and PharmaceuticsWound healingOsteonecrosis of the jawbusinessBiomedical reports
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Protection of Flupirtine on β-Amyloid-Induced Apoptosis in Neuronal Cells In Vitro: Prevention of Amyloid-Induced Glutathione Depletion

2002

Effective drugs are not available to protect against beta-amyloid peptide (A beta)-induced neurotoxicity. Cortical neurons from rat embryos were treated with the toxic fragment A beta25-35 at 1 microM in the presence or absence of flupirtine, a triaminopyridine, successfully applied clinically as a nonopiate analgesic drug. Five days later 1 microM A beta25-35 caused reduction of cell viability to 31.1%. Preincubation of cells with flupirtine (1 or 5 microg/ml) resulted in a significant increase of the percentage of viable cells (74.6 and 65.4%, respectively). During incubation with A beta25-35 the neurons undergo apoptosis as determined by appearance of the characteristic stepladder-like D…

Pathologymedicine.medical_specialtyCell SurvivalAminopyridinesApoptosisPharmacologymedicine.disease_causeBiochemistryAntioxidantsCellular and Molecular NeurosciencemedicineAnimalsViability assaySenile plaquesRats WistarCerebral CortexNeuronsAmyloid beta-PeptidesChemistryNeurotoxicitymedicine.diseaseGlutathionePeptide FragmentsRatsOxidative StressNeuroprotective AgentsApoptosisCell cultureDNA fragmentationFlupirtineOxidative stressmedicine.drugJournal of Neurochemistry
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