Search results for "biocompatibility"

showing 10 items of 233 documents

Tissue reaction to sealing materials: different view at biocompatibility

2010

Abstract The biodegradability of root canal sealers in areas other than the root canal system is crucial to the overall success rate of endodontic treatment. The aim of the present study was to investigate, the cell and tissue reaction to GuttaFlow and AHPlus, both in vitro and in vivo. For the in vitro experiments the materials were incubated with Human Periodontal Ligament Fibroblasts and cell proliferation and cytotoxicity analyses were performed. Additional fluorescence-microscope stainings were carried out in order to visualize cell growth and morphology. For assessment of the tissue reaction to the materials a subcutaneous implantation model in Wistar rats was employed and the inflamm…

Pathologymedicine.medical_specialtyBiocompatibilityPeriodontal LigamentRoot canallcsh:MedicineDentistryBiocompatible MaterialsDinoprostoneRoot Canal Filling MaterialsbiocompatibilityIn vivomedicineAnimalsHumansPeriodontal fiberRats WistarApical foramenCell Proliferationbusiness.industryChemistryResearchsealing materiallcsh:RbiomaterialGranulation tissueBiomaterialHistologyGeneral MedicineRatsmedicine.anatomical_structureAHPlusFemaleGuttaflowbusinessEuropean Journal of Medical Research
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Effect of Morphology and Size of Halloysite Nanotubes on Functional Pectin Bionanocomposites for Food Packaging Applications

2017

Pectin bionanocomposite films filled with various concentrations of two different types of halloysite nanotubes were prepared and characterized in this study as potential films for food packaging applications. The two types of halloysite nanotubes were long and thin (patch) (200-30 000 nm length) and short and stubby (Matauri Bay) (50-3000 nm length) with different morphological, physical, and dispersibility properties. Both matrix (pectin) and reinforcer (halloysite nanotubes) used in this study are considered as biocompatible, natural, and low-cost materials. Various characterization tests including Fourier transform infrared spectroscopy, field emission scanning electron microscopy, rele…

PectinScanning electron microscopeHalloysite nanotube02 engineering and technology01 natural sciencesPackaging machineContact angleBionanocompositeHeat resistanceGeneral Materials ScienceComposite materialSettore CHIM/02 - Chimica FisicapectinNanotubesYarn Antimicrobial filmFourier transform infrared spectroscopypatch halloysiteSalicylic acidDynamic mechanical analysis021001 nanoscience & nanotechnologyReinforcementPackagingPolyethylenepectin Kaoliniteantimicrobial filmPectinsAluminum SilicatesBiocompatibility0210 nano-technologyScanning electron microscopyMicroorganismMaterials sciencefood.ingredientBiocompatibilityengineering.materialDynamic mechanical analysi010402 general chemistryHalloysiteFood packagingfoodUltimate tensile strengthFourier transform infrared spectroscopyContact angleBacteriaField emission microscopeFunctional foodthermal resistanceHalloysite0104 chemical sciencesNanotubeBiological materialengineeringClayACS Applied Materials & Interfaces
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Propolis-Based Nanofiber Patches to Repair Corneal Microbial Keratitis

2021

In this research, polyvinyl-alcohol (PVA)/gelatin (GEL)/propolis (Ps) biocompatible nanofiber patches were fabricated via electrospinning technique. The controlled release of Propolis, surface wettability behaviors, antimicrobial activities against the S. aureus and P. aeruginosa, and biocompatibility properties with the mesenchymal stem cells (MSCs) were investigated in detail. By adding 0.5, 1, and 3 wt.% GEL into the 13 wt.% PVA, the morphological and mechanical results suggested that 13 wt.% PVA/0.5 wt.% GEL patch can be an ideal matrix for 3 and 5 wt.% propolis addition. Morphological results revealed that the diameters of the electrospun nanofiber patches were increased with GEL (from…

Pharmaceutical ScienceBiocompatible Materials02 engineering and technologyGelatinAnalytical ChemistryContact angleQD241-4410302 clinical medicineAnti-Infective AgentsSpectroscopy Fourier Transform InfraredDrug DiscoveryMesenchymal stem cell proliferationDrug CarriersChemistrySSCAFFOLDHYDROGELP<i>S. aureus</i>021001 nanoscience & nanotechnologyControlled releaseaeruginosaElectrospinningpropolisChemistry (miscellaneous)microbial keratitisPseudomonas aeruginosaBLINDNESSMolecular MedicineELECTROSPUN0210 nano-technologyStaphylococcus aureusfood.ingredient<i>P. aeruginosa</i>BiocompatibilitySurface PropertiesFABRICATIONMicrobial Sensitivity TestsCHEMICAL-COMPOSITIONaureusArticle03 medical and health sciencesfoodnanofibersPhysical and Theoretical Chemistrycorneal patchelectrospinningKeratitisCOMPOSITEGELATINOrganic ChemistryPropolisS. aureusDrug LiberationP. aeruginosaPolyvinyl AlcoholNanofiber030221 ophthalmology & optometryPROPERTYMEMBRANENuclear chemistry
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Methods of protein surface PEGylation under structure preservation for the emulsion-based formation of stable nanoparticles

2016

Proteins show remarkable versatility as multifunctional materials for therapeutic applications. They can be easily modified with the toolkit of bioorganic chemistry and are particularly attractive because of their degradability and biocompatibility. Herein, we evaluate different methods for the attachment of multiple PEG chains on the surface of the enzyme lysozyme. For this, we activated standard 2 kDa mPEG chains with four different electrophilic groups and tested their ability to react with different amino acids on the surface of our model protein. The aim was to find an effective and at the same time mild modification method that preserves the native structure and activity of the enzyme…

PharmacologyBiocompatibilityChemistryOrganic ChemistryPharmaceutical ScienceNanoparticle02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCombinatorial chemistry0104 chemical sciencesDrug DiscoveryEmulsionPEG ratioAmphiphilePEGylationMolecular MedicineBioorganic chemistryOrganic chemistrySolubility0210 nano-technologyMedChemComm
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Opportunities and Challenges of Fluorescent Carbon Dots in Translational Optical Imaging

2015

The fluorescent carbon dot (C-dot) is a new class of carbon nanomaterials. It has a discrete or quasispherical structure, typically measures less than 10 nm and contains sp(2)/sp(3) carbon, oxygen/nitrogen-based groups and surface-modified functional groups. Compared with semiconductor quantum dots (QDs), C-dots offer much lower toxicity and a better biocompatibility profile. Their other favorable features include easy and inexpensive synthesis and surface modification potential. C-dots can be morphologically classified into graphene-based quantum dots (GQDs) and amorphous carbon nanodots (ACNDs). Numerous methods have been developed to synthesize C-dots, and are mainly divided into 'top-do…

PharmacologyBiocompatibilityGrapheneCarbonizationOptical Imagingchemistry.chemical_elementNanotechnologyFerric CompoundsCarbonlaw.inventionchemistryAmorphous carbonlawQuantum dotQuantum DotsDrug DiscoveryAnimalsHumansSurface modificationNanodotCarbonFluorescent DyesCurrent Pharmaceutical Design
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Inulin Derivatives Obtained &lt;i&gt;Via&lt;/i&gt; Enhanced Microwave Synthesis for Nucleic Acid Based Drug Delivery

2015

A new class of therapeutic agents with a high potential for the treatment of different socially relevant human diseases is represented by Nucleic Acid Based Drugs (NABD), including small interfering RNAs (siRNA), decoy oligodeoxynucleotides (decoy ODN) and antisense oligonucleotides (ASOs). Although NABD can be engineered to be specifically directed against virtually any target, their susceptibility to nuclease degradation and the difficulty of delivery into target tissues severely limit their use in clinical practice and require the development of an appropriate nanostructured delivery system. For delivery of NABD, Inulin (Inu), a natural, water soluble and biocompatible polysaccharide, wa…

PharmacologyNucleaseBiocompatibilitybiologyChemistryClinical BiochemistryCombinatorial chemistrychemistry.chemical_compoundBiochemistryDrug DiscoveryDrug deliveryNucleic acidbiology.proteinMolecular MedicineAgaroseAmine gas treatingLuciferaseCytotoxicityCurrent Drug Targets
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Preparation of Poly(l-lactic acid) Scaffolds by Thermally Induced Phase Separation: Role of Thermal History

2018

Abstract Poly-L-Lactic Acid (PLLA) scaffolds for tissue engineering were prepared via thermally induced phase separation of a ternary system PLLA/dioxane/tetrahydrofurane. An extension to solution of a previously developed method for solidification from the melt was adopted, the technique being based on a Continuous Cooling Transformation (CCT) approach, consisting in recording the thermal history of rapidly cooled samples and analysing the resulting morphology. Different foams were produced by changing the thermal history, the dioxane to THF ratio (50/50, 70/30, 90/10 v/v) and the polymer concentration (2, 2.5, 4 ° wt) in the starting ternary solution. Pore size, porosity, melting and crys…

Poly l lactic acidPore sizeMorphology (linguistics)Materials sciencePolymers and PlasticsBiocompatibilitySpinodal decompositionGeneral Chemical Engineering02 engineering and technology010402 general chemistryMEMBRANES01 natural sciencesSPINODAL DECOMPOSITIONIndustrial and Manufacturing EngineeringBIOCOMPATIBILITYPOROUS SCAFFOLDSTISSUE REGENERATIONTissue engineeringMaterials ChemistryPOLYMERIC SCAFFOLDSTernary numeral systemPORE-SIZECELL TRANSPLANTATION021001 nanoscience & nanotechnology0104 chemical sciencesMembraneChemical engineeringMORPHOLOGY0210 nano-technologyBEHAVIOR
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Biocompatibility evaluation of PLLA scaffolds for vascular tissue engineering

2015

Poly-L-lactic acid (PLLA), a hemicrystalline material, has been extensively studied in applications of engineered tissues, because it is biodegradable, absorbable and it supports cell attachment and growth. The purpose of this study is to evaluate tissue/ material interactions, neovascularization and the biocompatibility of PLLA by optical and scanning electron microscopy in a model of animal implant. PLLA porous disks were implanted into the dorsal subcutis of BALB/C mice for 1, 2, 3, and 8 weeks. The bioptic samples of excised PLLA and the surrounding tissue were evaluated for inflammatory response and tissue ingrowth. The samples were divided in two halves: one was fixed in neutral buffe…

Poly-L-lactic acid; (PLLA); biocompatibility; immune responce; implant; scaffold; angiogenesisBiocompatibility PLLA scaffolds angiogenesis tissue engineering
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Gold nanostars coated with neutral and charged polyethylene glycols: A comparative study of in-vitro biocompatibility and of their interaction with S…

2015

Gold nanostars (GNS) have been coated with four different polyethylene glycols (PEGs) equipped with a -SH function for grafting on the gold surface. These PEGs have different chain lengths with average MW = 2000, 3000, 5000 and average number of -O-CH2-CH2 - units 44, 66, and 111, respectively. Two are neutral and two are terminated with -COOH and -NH2 functions, thus bearing negative and positive charges at physiological pH, thanks to the formation of carboxylate and ammonium groups. The negative charge of the GNS coated with PEG carboxylate has also been exploited to further coat the GNS with the PAH (polyallylamine hydrochloride) cationic polymer. Vitality tests have been carried out on …

Polyethylene glycolBiocompatibilityCell SurvivalMetal NanoparticlesPolyethylene glycolCell morphologyBiochemistryPolyethylene GlycolsInorganic Chemistrychemistry.chemical_compoundNeuroblastomaMicroscopy Electron TransmissionCell Line TumorPEG ratioOrganic chemistryHumansCarboxylatechemistry.chemical_classificationGold nanostarsMolecular StructureEndocytosiCationic polymerizationGold nanostarPolymerEndocytosisTwo-photon luminescenceNanomedicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiocompatibilityGoldPolyallylamine hydrochlorideNuclear chemistry
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New copolymers graft of α,β-poly(N-2-hydroxyethyl)-d,l-aspartamide obtained from atom transfer radical polymerization as vector for gene delivery

2012

Abstract New cationic α,β-poly(N-2-hydroxyethyl)- d , l -aspartamide (PHEA) graft copolymers were synthesized by ATRP, using diethylamino ethyl methacrylate (DEAEMA) as monomer for polymerization, yielding polycations (PHEA-pDEAEMA) able to condense DNA. Then, consecutive ATRP conditions were set up on PHEA-pDEAEMA to obtain copolymers containing also hydrophilic chains (PHEA-IB-pDMAEMA-pPEGMA) able to improve biocompatibility of polyplexes and to provide them stealth properties. Agarose gel studies showed that the copolymers effectively condensed plasmid DNA to form polyplexes. Light scattering studies were used to analyze the size and the ζ -potential of these polyplexes, showing that cop…

Polymers and PlasticsBiocompatibilityAtom-transfer radical-polymerizationGeneral Chemical EngineeringCationic polymerizationPHEA ATRP gene deliveryGeneral ChemistryBiochemistrychemistry.chemical_compoundMonomerchemistryPolymerizationPolymer chemistryMaterials ChemistryCopolymerSide chainEnvironmental ChemistryAgaroseReactive and Functional Polymers
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