Search results for "Polyesters"

showing 10 items of 117 documents

Antibacterial suture vs silk for the surgical removal of impacted lower third molars. A randomized clinical study.

2015

Background The aim of this study was to evaluate the clinical and microbiological impact of an antibacterial suture (Monocryl® Plus) in the surgical removal of I3M. Material and Methods A “split-mouth”, prospective pilot clinical study was designed involving 20 patients programmed for the surgical removal of I3M. Each side was randomly sutured with Monocryl® Plus or silk suture and removed for microbiological study 72 hours and 7 days after surgery. Presence of SSI, wound bleeding and the degree of discomfort associated with each type of suture material (scored by means of a visual analog scale) were evaluated. The level of contamination of each material was observed under the scanning elec…

MolarMaleDentistryInfection controlPilot Projectsmedicine.disease_causeDioxanes0302 clinical medicineSuture (anatomy)Control d'infeccionsPrevotella030212 general & internal medicineProspective StudiesbiologyTooth ImpactedDent molar:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saludPeptostreptococcusAnti-Bacterial AgentsDental surgeryUNESCO::CIENCIAS MÉDICASFemaleOral SurgeryAdultmedicine.medical_specialtyAdolescentVisual analogue scalePolyestersVeillonellaCirurgia dentalSilkOdontología03 medical and health sciencesYoung AdultOral surgerymedicineHumansGeneral DentistryCirurgia oralSuturesbusiness.industryResearch030206 dentistrybiology.organism_classificationMolarSurgeryOtorhinolaryngologyDental surgerySurgeryMolar ThirdbusinessStaphylococcusMedicina oral, patologia oral y cirugia bucal
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1-n-Butyl-3-methylimidazolium-2-carboxylate: a versatile precatalyst for the ring-opening polymerization of ε-caprolactone and rac-lactide under solv…

2013

The ring-opening polymerization of ε-caprolactone (ε-CL) and rac-lactide (rac-LA) under solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as precatalyst is described. Linear and star-branched polyesters were synthesized by successive use of benzyl alcohol, ethylene glycol, glycerol and pentaerythritol as initiator alcohols, and the products were fully characterized by 1H and 13C{1H} NMR spectroscopy, gel permeation chromatography (GPC), and differential scanning calorimetry (DSC). BMIM-2-CO2 acts as an N-heterocyclic carbene precursor, resulting from in situ decarboxylation, either by heating under vacuo (method A) or by addition of NaBPh4 (method B)…

N-heterocarbene precursorLactideLetterOrganic ChemistryRing-opening polymerizationPentaerythritollcsh:QD241-441chemistry.chemical_compoundChemistryimidazolium-2-carboxylateschemistryPolymerizationlcsh:Organic chemistryBenzyl alcoholgreen polymerization reactionPolymer chemistryaliphatic polyestersOrganic chemistrylcsh:QorganocatalysisCarboxylatelcsh:ScienceCaprolactoneEthylene glycolBeilstein Journal of Organic Chemistry
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Galactosylated polymeric carriers for liver targeting of sorafenib

2014

In this paper, we describe the preparation of liver-targeted polymeric micelles potentially able to carry sorafenib to hepatocytes for treatment of hepatocarcinoma (HCC), exploiting the presence of carbohydrate receptors, ASGPR. These micelles were prepared starting from a galactosylated polylactide-polyaminoacid conjugate. This latter was obtained by chemical reaction of α,β-poly(N-2-hydroxyethyl) (2-aminoethylcarbamate)-d,l-aspartamide (PHEA-EDA) with polylactic acid (PLA), and subsequent reaction with lactose, leading to PHEA-EDA-PLA-GAL copolymer. Liver-targeted sorafenib-loaded micelles were obtained in aqueous media at low PHEA-EDA-PLA-GAL copolymer concentration value with nanometer …

NiacinamideSorafenibBiodistributionPolyestersBiological AvailabilityPharmaceutical ScienceAntineoplastic AgentsPharmacologyKidneyMicellechemistry.chemical_compoundPolylactic acidHepatic cell-targeted carriersmedicineZeta potentialAnimalsLungneoplasmsMicellesDrug CarriersActive targetingPhenylurea CompoundsHepatic cell-targeted carrierGalactoseActive targeting; Galactosylation; Hepatic cell-targeted carriers; Polymeric micellesSorafenibEthylenediaminesdigestive system diseasesMice Inbred C57BLLiverBiochemistrychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoGalactosylationDrug deliveryPolymeric micellesFemalePeptidesDrug carrierSpleenmedicine.drugConjugateInternational Journal of Pharmaceutics
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P(HPMA)-block-P(LA) copolymers in paclitaxel formulations: Polylactide stereochemistry controls micellization, cellular uptake kinetics, intracellula…

2012

In order to explore the influence of polymer microstructure and stereochemistry in biological settings, the synthesis, micellization, cellular fate and the use in paclitaxel formulations of poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(L-lactide) (P(HPMA)-block-P(LLA)) and poly(N-(2-hydroxypropyl)-methacrylamide)-block-poly(DL-lactide) block copolymers (P(HPMA)-block-P(DLLA)) were studied. To this end, P(HPMA)-block-P(lactide) block copolymers and their fluorescently labeled analogues were synthesized. The polymers exhibited molecular weights M-n around 20,000 g/mol with dispersities (D=M-w/M-n) below 1.3. In addition, the solution conformation of this new type of partially degradable…

PaclitaxelStereochemistryCell SurvivalPolyestersTacticityMolecular ConformationPharmaceutical ScienceMicellechemistry.chemical_compoundTacticityAmphiphilePolymer chemistryPolylactide block copolymersCopolymerHumansReversible addition−fragmentation chain-transfer polymerizationMicelleschemistry.chemical_classificationLactideRAFT polymerizationPoly(N-(2-hydroxypropyl)-methacrylamideBiological TransportPolymerStructure activity relationshipAntineoplastic Agents PhytogenicKineticschemistryDrug deliveryHPMA block copolymersMethacrylatesHeLa Cells
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Adhesion prophylaxis using a copolymer with rationally designed material properties.

2008

Physical barriers are the only licensed adjuncts for adhesion prophylaxis in the United States and Europe. Here, we investigate D,L-polylactide-epsilon-caprolactonetrimethylenecarbonate (PCT copolymer), which is a rationally designed biomaterial, as an adhesion barrier.PCT copolymer membranes were produced by polymerization of the monomers, dissolution in organic solvents, and subsequently processing them by means of modified phase inversion and freeze drying. In vitro cytotoxicity was assayed by fibroblast culture. In vivo adhesion prophylaxis was studied in a rat model that involved standardized traumatization by electrocautery and suturing. The quantity and quality of the resulting adhes…

Pathologymedicine.medical_specialtyPolyestersBiocompatible MaterialsTissue AdhesionsFreeze-dryingSerous MembraneIn vivoMaterials TestingToxicity TestsCopolymermedicineAnimalsHumansRats WistarCells Culturedbusiness.industryBiomaterialMembranes ArtificialAdhesionAdhesion barrierIn vitroRatsMembraneWounds and InjuriesSurgeryLaparoscopybusinessBiomedical engineeringSurgery
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Margination of Fluorescent Polylactic Acid-Polyaspartamide based Nanoparticles in Microcapillaries In Vitro: the Effect of Hematocrit and Pressure.

2017

The last decade has seen the emergence of vascular-targeted drug delivery systems as a promising approach for the treatment of many diseases, such as cardiovascular diseases and cancer. In this field, one of the major challenges is carrier margination propensity (i.e., particle migration from blood flow to vessel walls); indeed, binding of these particles to targeted cells and tissues is only possible if there is direct carrier–wall interaction. Here, a microfluidic system mimicking the hydrodynamic conditions of human microcirculation in vitro is used to investigate the effect of red blood cells (RBCs) on a carrier margination in relation to RBC concentration (hematocrit) and pressure drop…

Pharmaceutical ScienceNanoparticle02 engineering and technologyPolymeric nanoparticleHematocrit01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundDrug Delivery SystemsPolylactic acidDrug Discoveryαβ-poly-(N-2-hydroxyethyl)-dl-aspartamide (PHEA)medicine.diagnostic_testMolecular StructureChemistry">l-aspartamide (PHEA)poly(ethylene glycol) (PEG)Microfluidic Analytical Techniques021001 nanoscience & nanotechnologypolymeric nanoparticlesBiochemistryHematocritmarginationChemistry (miscellaneous)Drug deliveryMolecular Medicine0210 nano-technologyDrug carrier">PolyestersIn Vitro Techniquesα β-poly-(N-2-hydroxyethyl)-D010402 general chemistryFluorescenceArticleMicrocirculationαβ-poly-(N-2-hydroxyethyl)-<span style="font-variant: small-caps;">d</span><span style="font-variant: small-caps;"></span><span style="font-variant: small-caps;">l</span>-aspartamide (PHEA); poly(lactic acid) (PLA); poly(ethylene glycol) (PEG); polymeric nanoparticles; marginationlcsh:QD241-441Rhodaminelcsh:Organic chemistrypoly(lactic acid) (PLA)PEG ratiomedicineHumansPhysical and Theoretical ChemistryParticle Sizeα β-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA)αβ-poly-(N-2-hydroxyethyl)-RhodaminesMicrocirculationOrganic Chemistry0104 chemical sciencesBiophysicsNanoparticles">dPeptidesMolecules (Basel, Switzerland)
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Nanosized shape-changing colloids from liquid crystalline elastomers.

2010

A method to prepare shape-changing nanospheres from liquid crystalline elastomers is reported. The nanosized colloids are prepared by a miniemulsion process. During this process, colloids are prepared from a liquid crystalline (LC) main-chain polyester and subsequently crosslinked into a nanometer-sized LC elastomer. The ability of these LC elastomers to change their shape at the phase transition temperature from the smectic A to the isotropic phase was detected by temperature-dependent transmission electron microscopy. The phase transition-induced shape change leads to strongly shape anisotropic nanosized elastomer particles.

Phase transitionMaterials sciencePolymers and PlasticsPolyestersdigestive oral and skin physiologyOrganic ChemistryNanoparticleElastomerLiquid CrystalsMiniemulsionPolyesterChemical engineeringElastomersTransmission electron microscopyPhase (matter)Polymer chemistryMaterials ChemistryNanoparticlessense organsParticle sizeColloidsParticle SizeMacromolecular rapid communications
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Establishment of a pulmonary epithelial barrier on biodegradable poly-L-lactic-acid membranes

2019

Development of biocompatible and functional scaffolds for tissue engineering is a major challenge, especially for development of polarised epithelia that are critical structures in tissue homeostasis. Different in vitro models of the lung epithelial barrier have been characterized using non-degradable polyethylene terephthalate membranes which limits their uses for tissue engineering. Although poly-L-lactic acid (PLLA) membranes are biodegradable, those prepared via conventional Diffusion Induced Phase Separation (DIPS) lack open-porous geometry and show limited permeability compromising their use for epithelial barrier studies. Here we used PLLA membranes prepared via a modification of the…

PhysiologyCell MembranesCell Culture TechniquesBiocompatible Materials02 engineering and technologyEpitheliumTissue engineeringAnimal CellsAbsorbable ImplantsMaterials TestingElectric ImpedanceMedicine and Health SciencesLungTissue homeostasisBarrier functionStaining0303 health sciencesMultidisciplinaryTissue ScaffoldsTight junctionPolyethylene TerephthalatesChemistryQRCell Staining021001 nanoscience & nanotechnologyMembrane StainingElectrophysiologyMembranePhysical SciencesMedicineCytokinesBiological CulturesCellular Structures and OrganellesJunctional ComplexesCellular TypesAnatomy0210 nano-technologyResearch ArticleCell PhysiologySciencePolyestersMaterials ScienceMaterial PropertiesResearch and Analysis MethodsMembrane PotentialPermeabilityCell LineTight Junctions03 medical and health sciencesCell AdhesionHumans030304 developmental biologyBiochemistry Genetics and Molecular Biology (all)Tissue EngineeringBiology and Life SciencesEpithelial CellsMembranes ArtificialCell BiologyCell CulturesBiological TissueAgricultural and Biological Sciences (all)Specimen Preparation and TreatmentCell culturePermeability (electromagnetism)BiophysicsCytokine secretionPLOS ONE
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Nanoencapsulation in Lipid-Core Nanocapsules Controls Mometasone Furoate Skin Permeability Rate and Its Penetration to the Deeper Skin Layers

2013

&lt;b&gt;&lt;i&gt;Aims:&lt;/i&gt;&lt;/b&gt; The influence of nanoencapsulation of mometasone furoate (MF) in poly(ε-caprolactone) lipid-core nanocapsules (LNC) on its in vitro human skin permeation and penetration was evaluated. &lt;b&gt;&lt;i&gt;Methods:&lt;/i&gt;&lt;/b&gt; Semisolid formulations were prepared by increasing the viscosity of LNC using a carbomer (Carbopol® Ultrez at 0.5% w/v). Two complementary techniques (the static Franz diffusion cell model and the Saarbrücken penetration model) were used to evaluate skin permeation/penetration. &lt;b&gt;&lt;i&gt;Results:&lt;/i&gt;&lt;/b&gt; The drug release rate was decreased by nanoencapsulation. The skin permeability of MF was control…

PhysiologyPolyestersSkin AbsorptionMometasone furoateHuman skinDermatologySkin permeabilityPharmacologyPermeabilityNanocapsulesNanocapsulesmedicineStratum corneumHumansParticle SizePregnadienediolsSkinPharmacologyintegumentary systemChemistryGeneral MedicinePenetration (firestop)PermeationLipidsmedicine.anatomical_structureSelf-healing hydrogelsMometasone Furoatemedicine.drugBiomedical engineeringSkin Pharmacology and Physiology
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Biodegradable tablets having a matrix of low molecular weight poly-L-lactic acid and poly-D,L-lactic acid.

1990

Biodegradable Homo- and Copolymers of lactic and glycolic acids have been used for manufacture of microparticles and matrix implants1,5). To ensure sufficient hydrolytic matrix stability lactic acids of high and medium degree of polymerization have been used. The manufacture of poly lactic acid tablets with an average molecular weight of 25000 and 6000 was reported recently, after finishing the following study2). Bioabbaubare Gerusttabletten aus niedermolekularer poly-L-Milchsaure und poly-D,L-Milchsaure

Poly l lactic acidChemistryPolymersMatrix stabilityPolyestersPharmaceutical ScienceStereoisomerismDegree of polymerizationLactic acidMatrix (chemical analysis)Molecular WeightHydrolysischemistry.chemical_compoundDrug DiscoveryCopolymerLactatesMolar mass distributionOrganic chemistryLactic AcidBiotransformationTabletsArchiv der Pharmazie
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