Search results for "Viability assay"

showing 10 items of 279 documents

Comparative evaluation of the impact on endothelial cells induced by different nanoparticle structures and functionalization

2015

In the research field of nanoparticles, many studies demonstrated a high impact of the shape, size and surface charge, which is determined by the functionalization, of nanoparticles on cell viability and internalization into cells. This work focused on the comparison of three different nanoparticle types to give a better insight into general rules determining the biocompatibility of gold, Janus and semiconductor (quantum dot) nanoparticles. Endothelial cells were subject of this study, since blood is the first barrier after intravenous nanoparticle application. In particular, stronger effects on the viability of endothelial cells were found for nanoparticles with an elongated shape in compa…

Materials scienceBiocompatibilitymedia_common.quotation_subjectJanus particlesGeneral Physics and AstronomyNanoparticleJanus particlesNanotechnologyquantum dotslcsh:Chemical technologylcsh:TechnologyFull Research PaperNanotechnologylcsh:TP1-1185General Materials ScienceViability assayElectrical and Electronic Engineeringlcsh:ScienceInternalizationNanoparticle Applicationcell viabilitymedia_commonlcsh:Tlcsh:QC1-999internalizationNanoscienceColloidal goldgold nanoparticlesSurface modificationlcsh:Qlcsh:PhysicsBeilstein Journal of Nanotechnology
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Inulin coated plasmonic gold nanoparticles as a tumor-selective tool for cancer therapy.

2015

Preferential uptake by cancer cells of PEG-inulin coated gold nanoparticles loaded with the drug doxorubicin.

Materials scienceBiomedical EngineeringNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesHeLamedicineFluorescence microscopeGeneral Materials ScienceDoxorubicinViability assayCytotoxicitybiologyMedicine (all)Chemistry (all)technology industry and agricultureCancerGeneral ChemistryGeneral Medicine021001 nanoscience & nanotechnologymedicine.diseasebiology.organism_classification0104 chemical sciences3. Good healthChemistryColloidal goldSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoCancer cellBiophysicsMaterials Science (all)0210 nano-technologymedicine.drugJournal of materials chemistry. B
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Cytotoxicity of Root Canal Filling Materials to Three Different Human Cell Lines

2001

The aim of this study was to investigate the biological compatibility of five root canal sealers (Sealapex, Endion, Super-EBA, Ketac-Endo, and AH Plus) and regular and calcium hydroxide-based gutta-percha in three different human cell lines. Cultures without root canal sealers were used as controls. Cell growth, cell morphology, cell viability, protein content of the cells, and prostaglandin E 2 (PGE 2 ) release were used as parameters to determine the cytotoxicity of the materials. The protein content of the three cell lines—nasal fibroblasts, gingival fibroblasts, and epithelial tumor cells—was significantly reduced (p ≤ 0.001) by all materials tested. Determinations of PGE 2 release show…

Materials scienceCell SurvivalRoot canalmedicine.medical_treatmentStatistics as TopicCellGingivaDentistryBiocompatible MaterialsCell morphologyDinoprostoneCell LineCalcium HydroxideRoot Canal Filling Materialschemistry.chemical_compoundTumor Cells CulturedmedicineHumansNeoplasms Glandular and EpithelialViability assayCytotoxicityGeneral DentistryCalcium hydroxideEpoxy ResinsCell growthbusiness.industryProteinsFibroblastsMolecular biologySalicylatesNasal Mucosamedicine.anatomical_structurechemistryGlass Ionomer CementsDentin-Bonding AgentsGutta-PerchabusinessBiomarkersCell DivisionProstaglandin EJournal of Endodontics
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Optimization of Cell Growth on Bacterial Cellulose by Adsorption of Collagen and Poly-L-Lysine

2015

Poly-L-lysine and collagen were separately added to bacterial cellulose (BC) nanofibers. The ionic surface charge had been previously modified in order to promote the adsorption of poly-L-lysine and collagen. Cell adhesion of Chinese hamster ovary (CHO) cells on BC surfaces was confirmed by removing unattached cells from the BC substrates. Cell viability was calculated and it was determined that both poly-L-lysine-BC and collagen-BC substrates are viable for cell growth. The results showed that the cell viability in poly-L-lysine modified BC substrate is similar to the one observed in polystyrene tissue culture plates.

Materials sciencePolymers and PlasticsCell growthGeneral Chemical EngineeringChinese hamster ovary cellSubstrate (chemistry)complex mixturesAnalytical Chemistrychemistry.chemical_compoundTissue cultureAdsorptionchemistryBiochemistryBacterial celluloseBiophysicsbacteriaViability assayCell adhesionInternational Journal of Polymeric Materials and Polymeric Biomaterials
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Protective effect of bioaccessible fractions of citrus fruit pulps against H2O2-induced oxidative stress in Caco-2 cells

2017

Fruit pulps from Navel (N) and Cara Cara (CC) oranges, and Clementine mandarin freshly harvested (M) and refrigerated stored (M12) were used to evaluate the cytoprotective effect of their bioaccessible fractions (BF) against H2O2-induced oxidative stress in Caco-2 cells. BF of samples preserved viability vs. H2O2 treated cells, reaching values similar to controls. Lipid peroxidation was reduced to levels of control cells, but M did not reach control values. ROS and mitochondrial membrane potential changes (Δψm) values were reduced compared with H2O2 treated cells, but without achieving control levels. A significant reduction in cell proportions in G1 phase and a significant increase in sub-…

Membrane potentialChemistryIn vitro digestion04 agricultural and veterinary sciencesCell cyclemedicine.disease_cause040401 food scienceBioactive compoundsAntioxidantsLipid peroxidationchemistry.chemical_compound0404 agricultural biotechnologyBiochemistryCaco-2ApoptosisOxidative stressmedicineViability assayFood scienceCitrus fruit pulpsCaco-2 cellsOxidative stressFood ScienceCitrus fruit
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Influence of cell-cell contact between L. thermotolerans and S. cerevisiae on yeast interactions and the exo-metabolome

2019

International audience; Sequential fermentation of grape must inoculated with L. thermotolerans and then S. cerevisiae 24 h later (typical wine-making practice) was conducted with or without cell-cell contact between the two yeast species. We monitored cell viability of the two species throughout fermentation by flow cytometry. The cell viability of S. cerevisiae decreased under both conditions, but the decrease was greater if there was cell-cell contact. An investigation of the nature of the interactions showed competition between the two species for nitrogen compounds, oxygen, and must sterols. Volatile-compound analysis showed differences between sequential and pure fermentation and that…

MetaboliteL. thermotoleransInteractionsS. cerevisiaeWineSaccharomyces cerevisiaeMicrobiologyFlow cytometry03 medical and health scienceschemistry.chemical_compoundMetabolomicsMetabolomemedicineMetabolomics[CHIM]Chemical SciencesVitisViability assayFlow cytometryCell-cell contact030304 developmental biology0303 health sciencesCell cell contactMicrobial Viabilitymedicine.diagnostic_testEthanol030306 microbiologyChemistryfood and beveragesYeastCoculture TechniquesOxygenBiochemistryInteractions ; S. Cerevisiae ; L. Thermotolerans ; Cell-cell Contact ; Flow Cytometry ; MetabolomicsFermentationSaccharomycetalesMetabolomeMicrobial InteractionsFermentationFood Science
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Approaches to study yeast cell aging and death

2014

For millennia, yeast has been exploited to obtain fermentation products, such as foods and beverages. For c. 50 years, yeast has been an established model organism for basic and applied research, and more specifically, for c. 15 years, this unicellular organism has been applied to dissect molecular mechanisms of cell aging and programmed cell death. In this review, we present an overview of approaches to study cell aging and death in yeast, including lifespan assessments, calorie restriction, cell viability, survival, and death markers.

Microbiological TechniquesProgrammed cell deathTime FactorsCell Deathved/biologyved/biology.organism_classification_rank.speciesCalorie restrictionSaccharomyces cerevisiaeMycologySaccharomyces cerevisiaeGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyUnicellular organismYeastCell biologyyeast aging. chronological aging methods in yeast geneticsSettore BIO/13 - Biologia ApplicataViability assayModel organismCell agingFEMS Yeast Research
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Biocompatibility of three new calcium silicate-based endodontic sealers on human periodontal ligament stem cells.

2016

Aim To evaluate the biocompatibility of three calcium silicate-based endodontic sealers, Bioroot BC Sealer (Septodont, Saint-Maur-des-Fosses, France), Endoseal MTA (EndoSeal, Maruchi, Seoul, Korea) and Nano-ceramic Sealer (B&L Biotech, Fairfax, VA, USA) (NCS), on human periodontal ligament stem cells (hPDLSCs). Methodology Human periodontal ligament stem cells were cultured in the presence of various endodontic sealer eluates for 24 h. Cell viability was determined using the MTT assay. Cell death and changes in phenotype induced by the set endodontic sealer eluates were evaluated through flow cytometry. Also, an in vitro scratch wound-healing model was used to determine their effects in cel…

Mineral trioxide aggregateBiocompatibilityPeriodontal ligament stem cellsPeriodontal LigamentDentistry02 engineering and technologyCell morphologyEndodonticsRoot Canal Filling Materials03 medical and health sciences0302 clinical medicineCell MovementMaterials TestingPeriodontal fiberHumansMTT assayViability assayGeneral DentistryCells CulturedCell Proliferationbusiness.industryCell growthChemistrySilicatesStem Cells030206 dentistryCalcium Compounds021001 nanoscience & nanotechnologyMolecular biology0210 nano-technologybusinessInternational endodontic journal
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Thermo-setting glass ionomer cements promote variable biological responses of human dental pulp stem cells.

2017

To evaluate the in vitro cytotoxicity of Equia Forte (GC, Tokyo, Japan) and Ionostar Molar (Voco, Cuxhaven, Germany) on human dental pulp stem cells (hDPSCs).hDPSCs isolated from third molars were exposed to several dilutions of Equia Forte and Ionostar Molar eluates (1/1, 1/2 and 1/4). These eluates were obtained by storing material samples in respective cell culture medium for 24h (n=40). hDPSCs in basal growth culture medium were the control. Cell viability and cell migration assays were performed using the MTT and wound-healing assays, respectively. Also, induction of apoptosis and changes in cell phenotype were evaluated by flow cytometry. Changes in cell morphology were analysed by im…

MolarMaterials scienceCell SurvivalGlass ionomer cementApoptosis02 engineering and technologyFlow cytometry03 medical and health sciences0302 clinical medicineCell MovementDental pulp stem cellsMaterials TestingmedicineHumansGeneral Materials ScienceViability assayGeneral DentistryCells CulturedDental Pulpmedicine.diagnostic_testCell growthSpectrophotometry AtomicStem CellsSpectrometry X-Ray Emission030206 dentistry021001 nanoscience & nanotechnologyFlow CytometryMolecular biologyStainingPhenotypeMechanics of MaterialsCell cultureGlass Ionomer CementsMicroscopy Electron ScanningMolar Third0210 nano-technologyDental materials : official publication of the Academy of Dental Materials
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Grafting TRAIL through Either Amino or Carboxylic Groups onto Maghemite Nanoparticles: Influence on Pro-Apoptotic Efficiency

2021

International audience; Tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL) is a member of the TNF cytokine superfamily. TRAIL is able to induce apoptosis through engagement of its death receptors DR4 and DR5 in a wide variety of tumor cells while sparing vital normal cells. This makes it a promising agent for cancer therapy. Here, we present two different ways of covalently grafting TRAIL onto maghemite nanoparticles (NPs): (a) by using carboxylic acid groups of the protein to graft it onto maghemite NPs previously functionalized with amino groups, and (b) by using the amino functions of the protein to graft it onto NPs functionalized with carboxylic acid groups. The two …

Molecular modelGeneral Chemical EngineeringCarboxylic acidmedicine.medical_treatment02 engineering and technologyArticlelcsh:Chemistry03 medical and health sciencesmedicine[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyGeneral Materials Science[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyViability assaycancer diseasecell viability030304 developmental biologysurface functionalizationchemistry.chemical_classification0303 health sciencesChemistrymolecular modelingtechnology industry and agriculture021001 nanoscience & nanotechnologyLigand (biochemistry)3. Good healthmaghemiteCytokinelcsh:QD1-999BiochemistryApoptosisCell cultureTumor necrosis factor alpha0210 nano-technology
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