Search results for "CELL SURVIVAL"

showing 10 items of 870 documents

Agarose/κ-carrageenan-based hydrogel film enriched with natural plant extracts for the treatment of cutaneous wounds.

2020

Abstract Hydrogels for complex and chronic wound dressings must be conformable, absorb and retain wound exudates and maintain hydration. They can incorporate and release bioactive molecules that can accelerate the healing process. Wound dressings have to be in contact with the wound and epidermis, even for long periods, without causing adverse effects. Hydrogel dressing formulations based on biopolymers derived from terrestrial or marine flora can be relatively inexpensive and well tolerated. In the present article hydrogel films composed by agarose (1.0 wt%), κ-carrageenan at three different concentrations (0.5, 1.0 and 1.5 wt%) and glycerol (3.0 wt%) were prepared without recourse to cros…

Chronic woundCell Survival02 engineering and technologyCarrageenanBiochemistryAntioxidants03 medical and health scienceschemistry.chemical_compoundMiceStructural BiologymedicineGlycerolAnimalsFibroblastCytotoxicityMolecular Biology030304 developmental biology0303 health sciencesEpidermis (botany)Plant ExtractsSepharoseGeneral MedicineFibroblasts021001 nanoscience & nanotechnologyMethylgalactosidesBandagesBryopsidaElasticityBiomechanical Phenomenamedicine.anatomical_structureAgarose/κ-carrageenan lend Cryphaea heteromalla bryophyte Wound healingchemistrySelf-healing hydrogelsBiophysicsNIH 3T3 CellsAgaroseSettore CHIM/07 - Fondamenti Chimici Delle Tecnologiemedicine.symptomSwelling0210 nano-technologyInternational journal of biological macromolecules
researchProduct

Relationship between mutagenicity and DNA adduct formation in mammalian cells for fjord- and bay-region diol-epoxides of polycyclic aromatic hydrocar…

1991

Abstract Chinese hamster V79 cells were treated with the anti- and syn-diastereomers of the bay- or fjord-region diol-epoxides of four polycyclic aromatic hydrocarbons, namely benzo[a]pyrene (BP), benzo[c]chrysene (BcC), benzo[g]chrysene (BgC) and benzo[c]phenanthrene (BcPh). The frequency of induction of 6-thioguanine-resistant mutations was determined, and the extent of formation of DNA adducts was measured by 32P-postlabelling. When expressed as mutation frequency per nanomoles compound per millilitre incubation medium, this group of chemicals expressed a 160-fold range in potency. In agreement with previous experimental studies, the anti-diol-epoxide of BcC was highly mutagenic, inducin…

ChryseneStereochemistryCell SurvivalBenzo(c)phenanthreneToxicologyAdductchemistry.chemical_compoundCricetulusIsomerismCricetinaepolycyclic compoundsBenzo(a)pyreneAnimalsheterocyclic compoundsPolycyclic CompoundsMutation frequencyCells Culturedintegumentary systemorganic chemicalsfungiGeneral MedicineDNAPhenanthrenechemistryBenzo(a)pyreneMutationPyreneDNAMutagensChemico-biological interactions
researchProduct

Role of Seroalbumin in the Cytotoxicity of cis-Dichloro Pt(II) Complexes with (N^N)-Donor Ligands Bearing Functionalized Tails

2018

Given the potent anticancer properties of cisdiamminedichloroplatinum( II) and knowing its mode of action, we synthesized four new cis-[PtCl2(N^N)] organoplatinum complexes, two with N-substituted pbi ligands (pbiR = 1-R-2-(2-pyridyl)benzimidazole) (namely, 1 and 2) and two more with 4,4′-disubstituted bpy ligands (bpy = 2,2′-bipyridine) (namely, 3 and 4). We explored their cytotoxicity and ability to bind to deoxyguanosine monophosphate (dGMP), DNA, and albumin models. By 1H NMR and UV−vis spectroscopies, circular dichroism, agarose gel electrophoresis, differential scanning calorimetry measurements, and density functional theory calculations, we verified that only 3 can form aquacomplex s…

Circular dichroismCell SurvivalStereochemistryLigandPlasma protein bindingHeLa CellLigands010402 general chemistry01 natural sciencesChemistry Physical and theoreticalInorganic ChemistryHeLaBipyridinechemistry.chemical_compoundDrug StabilityCoordination ComplexesQuímica físicaHumansPhysical and Theoretical ChemistryCytotoxicityA549 CellOrganoplatinumPlatinumCoordination ComplexeCalorimetry Differential ScanningMolecular Structurebiology010405 organic chemistryChemistryRational designDeoxyguanine NucleotidesSerum Albumin BovineDNAbiology.organism_classification0104 chemical sciencesSettore CHIM/03 - Chimica Generale E InorganicaA549 CellsAgarose gel electrophoresisDeoxyguanine NucleotideHumanHeLa CellsProtein BindingInorganic Chemistry
researchProduct

Halloysite nanotubes-carbon dots hybrids multifunctional nanocarrier with positive cell target ability as a potential non-viral vector for oral gene …

2019

Abstract Hypothesis The use of non-viral vectors for gene therapy is hindered by their lower transfection efficiency and their lacking of self-track ability. Experiments This study aims to investigate the biological properties of halloysite nanotubes-carbon dots hybrid and its potential use as non-viral vector for oral gene therapy. The morphology and the chemical composition of the halloysite hybrid were investigated by means of high angle annular dark field scanning TEM and electron energy loss spectroscopy techniques, respectively. The cytotoxicity and the antioxidant activity were investigated by standard methods (MTS, DPPH and H2O2, respectively) using human cervical cancer HeLa cells …

Circular dichroismCell SurvivalSurface PropertiesStatic ElectricityAdministration Oral02 engineering and technologyCellular imagingengineering.material010402 general chemistry01 natural sciencesHalloysiteAntioxidantsBiomaterialsHeLaColloid and Surface ChemistryDynamic light scatteringFluorescence microscopeTumor Cells CulturedCarbon dotsAnimalsHumansParticle SizeSettore CHIM/02 - Chimica FisicaDrug CarriersbiologyMolecular StructureHalloysite nanotubesChemistryNanotubes CarbonOptical ImagingGene Transfer TechniquesTransfectionDNASettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologybiology.organism_classificationDark field microscopyDNA interaction0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHalloysite nanotubes Carbon dots DNA interaction Cellular imagingengineeringBiophysicsCattleNanocarriers0210 nano-technologyPorosityHeLa Cells
researchProduct

Micronucleus frequencies and clonogenic cell survival in TK6 cells exposed to changing dose rates under controlled temperature conditions.

2014

In most exposure scenarios the dose rate of exposure is not constant. Despite this, very little information exists on the possible biological effects of exposing cells to radiation under the conditions of a changing dose rate. The current study highlights interesting effects following exposure under these conditions.We constructed a new exposure facility that allows exposing cells inside an incubator and used it to irradiate human lymphoblastoid TK6 cells both after a moderate (0.48 Gy) and a high (1.1 Gy) dose, where the change in dose rate was, respectively, ≈ 17-fold (2.2-37 mGy/min) and ≈ 39-fold (2.7-106 mGy/min). Clonogenic survival and micronuclei (MN) induction were the chosen endpo…

Clonogenic survivalDNA RepairCell SurvivalBiologyCell LineAndrologyRadiation IonizingHumansRadiology Nuclear Medicine and imagingLymphocytesPoisson DistributionInterphaseCytokinesisChromosome AberrationsMicronucleus TestsRadiological and Ultrasound TechnologyLymphoblastX-RaysTemperatureDose-Response Relationship RadiationClonogenic cellArea Under CurveImmunologyMicronucleus testDose rateMicronucleusModerate-DoseDNA DamageInternational journal of radiation biology
researchProduct

Quantitative Analysis of Dynamic Association in Live Biological Fluorescent Samples

2014

Determining vesicle localization and association in live microscopy may be challenging due to non-simultaneous imaging of rapidly moving objects with two excitation channels. Besides errors due to movement of objects, imaging may also introduce shifting between the image channels, and traditional colocalization methods cannot handle such situations. Our approach to quantifying the association between tagged proteins is to use an object-based method where the exact match of object locations is not assumed. Point-pattern matching provides a measure of correspondence between two point-sets under various changes between the sets. Thus, it can be used for robust quantitative analysis of vesicle …

Computer and Information SciencesFluorescence-lifetime imaging microscopyMatching (graph theory)Cell SurvivalImage ProcessingAssociation (object-oriented programming)SciencerakkulatBioinformaticsTime-Lapse ImagingFluorescenceImage (mathematics)cellular structuresfluorescence imagingCell Line TumorMolecular Cell BiologyalgoritmitHumansComputer SimulationkuvantamismenetelmätPhysicsta113MicroscopyvesiclesMultidisciplinarySoftware Toolsbusiness.industryCytoplasmic VesiclesQRta1182Biology and Life SciencesSoftware EngineeringColocalizationExperimental dataPattern recognitionCell BiologyObject (computer science)imaging techniquesMolecular ImagingfluoresenssimikroskopiaSignal ProcessingEngineering and TechnologyMedicineArtificial intelligenceCellular Structures and OrganellesbusinessVesicle localizationResearch ArticlePLoS ONE
researchProduct

Cell inactivation and membrane damage after long-term treatments at sub-zero temperature in the supercooled and frozen states.

2008

The survival of cells subjected to cooling at sub-zero temperature is of paramount concern in cryobiology. The susceptibility of cells to cryopreservation processes, especially freeze-thawing, stimulated considerable interest in better understanding the mechanisms leading to cell injury and inactivation. In this study, we assessed the viability of cells subjected to cold stress, through long-term supercooling experiments, versus freeze-thawing stress. The viability of Escherichia coli, Saccharomyces cerevisiae, and leukemia cells were assessed over time. Supercooled conditions were maintained for 71 days at -10 degrees C, and for 4 h at -15 degrees C, and -20 degrees C, without additives or…

CryobiologyCell Membrane PermeabilityTime FactorsMembrane permeabilityOsmotic shockCell Survival[SDV]Life Sciences [q-bio]BioengineeringSaccharomyces cerevisiaeApplied Microbiology and BiotechnologyCryopreservation03 medical and health sciences[SPI]Engineering Sciences [physics]Cell Line TumorCongelation[ SPI ] Engineering Sciences [physics]Escherichia coliHumansViability assayComputingMilieux_MISCELLANEOUS030304 developmental biologyCryopreservation0303 health sciencesMicrobial Viability[ SDV ] Life Sciences [q-bio]Chemistry030302 biochemistry & molecular biologyCell MembraneMembraneBiophysicsWater of crystallizationBiotechnologyBiotechnology and bioengineering
researchProduct

Vitrification of human mature oocytes in clinical practice.

2009

Oocyte cryopreservation has long been the focus of unsuccessful efforts to perfect its clinical application. Lately, vitrification has been shown to provide high degrees of success by different research groups. This review attempts to address the efficiency of oocyte vitrification in clinical practice through an analysis of reports of IVF cycles in which embryo transfers have been conducted with vitrified metaphase-II human oocytes.

CryopreservationResearch groupsCell SurvivalObstetrics and GynecologyOocyte cryopreservationFertilization in VitroBiologyOocyteEmbryo TransferClinical PracticeAndrologymedicine.anatomical_structureTreatment OutcomeReproductive MedicinePregnancymedicineOocytesHumansVitrificationFemaleDevelopmental BiologyReproductive biomedicine online
researchProduct

Test system for trifunctional antibodies in 3D MCTS culture.

2009

The aim of the present study was to assess the feasibility of a 3D tumor cell culture model, that is, multicellular tumor spheroids (MCTSs) as an adequate model for micrometastases and therefore as a pharmacological model for efficacy testing of trifunctional therapeutic antibodies. Unlike conventional monolayer cultures, spheroids allow researchers to study parameters, such as 3D cell shape, 3D cell arrangement and microenvironment, and penetration efficiency of defense cells that may largely influence the efficacy of antibody treatment in vivo. The authors established a long-term coculture of human MCTSs with peripheral blood mononuclear cells (PBMCs) to test the anticancer effect of the …

Culture modelAntibodies NeoplasmCell SurvivalCellCatumaxomabCell Culture TechniquesApoptosisEfficiencyBiochemistryPeripheral blood mononuclear cellCancer VaccinesAnalytical ChemistryIn vivoSpheroids CellularAntibodies BispecificmedicineTumor Cells CulturedHumansCell ProliferationbiologySpheroidTrifunctional antibodymedicine.anatomical_structureHead and Neck NeoplasmsImmunologybiology.proteinCancer researchCarcinoma Squamous CellMolecular MedicineImmunotherapyAntibodyBiotechnologymedicine.drugJournal of biomolecular screening
researchProduct

The effect of light curing units and modes on cytotoxicity of resin-core systems

2010

Objective: The aim of this study was to compare the cytotoxic effects of various resin-based core materials that were cured with three light curing units (LCUs) in different modes on L?929 mouse fibroblast cells over 24 h and 72 h periods. Study design: Eighty-four cylindrical discs (2 mm in thickness and 6 mm in diameter) of each material (Rebilda, Voco; Build-It FR, Pentron; Clearfil DC Core, Kuraray and Bis-core, Bisco) were cured by QTH LCU (soft-up and high-power modes), LED LCU (exponential and standard modes) and PAC LCU (normal and ramp-curing modes). Then the samples were aged for 24 and 72 hours in Dulbecco?s Modified Eagle Medium/Ham?s F12 (DMEM/F12). After each ageing interval, …

Curing Lights DentalChemistryFibroblasts:CIENCIAS MÉDICAS [UNESCO]Light curingMultifactorial analysisMiceResins SyntheticOtorhinolaryngologyUNESCO::CIENCIAS MÉDICASPure cultureAnimalsSurgeryMouse FibroblastCytotoxicityGeneral DentistryCell survivalCuring (chemistry)Nuclear chemistry
researchProduct