Search results for "Poloxamer"

showing 10 items of 27 documents

Cytotoxicity and chemosensitizing activity of amphiphilic poly(glycerol)-poly(alkylene oxide) block copolymers.

2014

All polymeric chemosensitizers proposed thus far have a linear poly(ethylene glycol) (PEG) hydrophilic block. To testify whether precisely this chemical structure and architecture of the hydrophilic block is a prerequisite for chemosensitization, we tested a series of novel block copolymers containing a hyperbranched polyglycerol segment as a hydrophilic block (PPO-NG copolymers) on multi-drug-resistant (MDR) tumor cells in culture. PPO-NG copolymers inhibited MDR of three cell lines, indicating that the linear PEG can be substituted for a hyperbranched polyglycerol block without loss of the polymers' chemosensitizing activity. The extent of MDR reversal increased with the polymers affinity…

GlycerolPolymers and PlasticsCell SurvivalPolymersBioengineeringAntineoplastic AgentsMicellePolyethylene GlycolsBiomaterialschemistry.chemical_compoundInhibitory Concentration 50Polymer chemistryAmphiphilePEG ratioMaterials ChemistryCopolymerHumansATP Binding Cassette Transporter Subfamily B Member 1CytotoxicityMicelleschemistry.chemical_classificationDrug SynergismPolymerPoloxamerDrug Resistance MultiplechemistryDoxorubicinDrug Resistance NeoplasmMCF-7 CellsDrug Screening Assays AntitumorK562 CellsEthylene glycolHydrophobic and Hydrophilic InteractionsBiomacromolecules
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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Synergistic behavior of poly(aspartic acid) and Pluronic F127 in aqueous solution as studied by viscometry and dynamic light scattering.

2012

Abstract Pluronic F127/poly(aspartic acid) mixtures were investigated in dilute solutions by viscometry and dynamic light scattering. The two polymers were chosen due to well known applications in biomedical field, taking into account the final purpose (the use of the complex structure as drug delivery systems). The central item was to identify the possibility of complexation between the poly(carboxylic acid) and a non-ionic polymer and to investigate the conditions of the interpolymer complex formation. The ability of Pluronic F127 to form micelle is well known. Poly(aspartic acid), as a polycarboxylic acid with resemblance with polyacrylic acid, can act as dispersant, antiscalant, superab…

LightCarboxylic acidIntrinsic viscosityStatic ElectricityPoloxamerMicellechemistry.chemical_compoundColloid and Surface ChemistryDynamic light scatteringAspartic acidPolymer chemistryScattering RadiationPhysical and Theoretical Chemistrychemistry.chemical_classificationAqueous solutionViscosityPolyacrylic acidWaterSurfaces and InterfacesGeneral MedicinePolymerSolutionschemistryPeptidesRheologyBiotechnologyColloids and surfaces. B, Biointerfaces
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Dissolution and dissolution/permeation experiments for predicting systemic exposure following oral administration of the BCS class II drug clarithrom…

2017

In order to save time and resources in early drug development, in vitro methods that correctly predict the formulation effect on oral drug absorption are necessary. The aim of this study was to 1) evaluate various BCS class II drug formulations with in vitro methods and in vivo in order to 2) determine which in vitro method best correlates with the in vivo results. Clarithromycin served as model compound in formulations with different particle sizes and content of excipients. The performed in vitro experiments were dissolution and dissolution/permeation experiments across two types of membrane, Caco-2 cells and excised rat intestinal sheets. The in vivo study was performed in rats. The oral…

MaleCell Membrane PermeabilityChemistry PharmaceuticalAdministration OralPharmaceutical ScienceExcipient02 engineering and technologyAbsorption (skin)030226 pharmacology & pharmacyExcipients03 medical and health sciences0302 clinical medicineIn vivoClarithromycinmedicineAnimalsHumansIntestinal MucosaRats WistarSolubilityDissolutionChromatographyChemistryPermeation021001 nanoscience & nanotechnologyRatsMucusIntestinal AbsorptionSolubilityPoloxamer 407Caco-2 Cells0210 nano-technologyEx vivomedicine.drugEuropean Journal of Pharmaceutical Sciences
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Pluronic nanoparticles as anti-oxidant carriers for polymers

2016

Abstract The immobilization of anti-oxidant stabilizers for polymers, particularly naturally occurring systems, can be considered a valuable route for preventing their migration, volatilization, thermo-degradation and decomposition at typical high processing temperatures, as well as for enhance their solubility in polymers. In this work, an innovative approach for the immobilization of naturally occurring stabilizer, through the encapsulation in copolymer nanoparticles, is proposed. Pluronic nanoparticles (PNPs), based on PEO-PPO-PEO, (PEO: poly (ethylene oxide); PPO: poly(propylene oxide)), without and with quercetin, Q, have been successfully formulated and the critical micellar condition…

Materials Chemistry2506 Metals and AlloysAnti-oxidant carrierMaterials sciencePEO-PPO-PEO nanoparticlePolymers and PlasticsNanoparticle02 engineering and technologyCondensed Matter Physic010402 general chemistry01 natural scienceschemistry.chemical_compoundDynamic light scatteringPolymer chemistryMaterials ChemistryPhoto-oxidationMechanics of MaterialPropylene oxideSolubilitychemistry.chemical_classificationPolymers and PlasticEthylene oxideAnti-oxidant carrier; PEO-PPO-PEO nanoparticles; Photo-oxidation; Condensed Matter Physics; Mechanics of Materials; Polymers and Plastics; Materials Chemistry; 2506; Metals and Alloystechnology industry and agricultureMetals and AlloysPolymerPoloxamer021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical scienceschemistryChemical engineeringMechanics of MaterialsPEO-PPO-PEO nanoparticles25060210 nano-technologyEthylene glycol
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Polymeric micelles as a new generation of anti-oxidant carriers

2017

A promising strategy to immobilize a natural stabilizer in polymeric films is presented. Par-Ticularly, nevadensin (N, a natural basil flavonoid) molecules have been encapsulated in Pluronic F-127 micelles [F127, a triblock copolymer poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide)] and the obtained nanoparticles have been introduced in poly(ethylene glycol), PEG [otherwise known as poly(ethylene oxide), PEO]. In order to verify the effectiveness of the micelles as anti-oxidant carriers, PEG-based films have been subjected to artificial weathering. The encapsulation of anti-oxidant molecules allows the enhancement of N solubility in PEG, leading to advanced materials with enh…

Materials Chemistry2506 Metals and AlloysAnti-oxidant carrierPhoto-oxidative stabilityPolymers and PlasticsGeneral Chemical EngineeringPoly(ethylene oxide)Nanoparticlemacromolecular substances02 engineering and technology01 natural sciencesMicellechemistry.chemical_compoundAnti-oxidant carriers; Photo-oxidative stability; Poly(ethylene oxide); Polymeric micelles; Chemical Engineering (all); Polymers and Plastics; Materials Chemistry; 2506; Metals and AlloysPolymeric micellePEG ratioCopolymerMaterials ChemistryChemical Engineering (all)Propylene oxidePolymers and PlasticEthylene oxidetechnology industry and agricultureMetals and AlloysPoloxamer021001 nanoscience & nanotechnology010406 physical chemistry0104 chemical scienceschemistryChemical engineeringPolymeric micelles25060210 nano-technologyAnti-oxidant carriersEthylene glycol
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Functional response of novel bioprotective poloxamer-structured vesicles on inflamed skin

2017

[EN] Resveratrol and gallic acid, a lipophilic and a hydrophilic phenol, were co-loaded in innovative, biocompatible nanovesicles conceived for ensuring the protection of the skin from oxidative-and inflammatory-related affections. The basic vesicles, liposomes and glycerosomes, were produced by a simple, one-step method involving the dispersion of phospholipid and phenols in water or water/glycerol blend, respectively. Liposomes and glycerosomes were modified by the addition of poloxamer, a stabilizer and viscosity enhancer, thus obtaining viscous or semisolid dispersions of structured vesicles. The vesicles were spherical, unilamellar and small in size (similar to 70 nm in diameter). The …

Materials scienceCell SurvivalSwineSkin AbsorptionBiomedical EngineeringPhospholipidPharmaceutical ScienceMedicine (miscellaneous)Bioengineering02 engineering and technologyPoloxamerResveratrol010402 general chemistry01 natural sciencesCell Linechemistry.chemical_compoundMiceIn vivoGallic AcidStilbenesGlycerolAnimalsEdemaGeneral Materials SciencePhenolsSkinLiposomePhenolVesicleAnti-Inflammatory Agents Non-SteroidalSkin inflammationPoloxamerFibroblasts021001 nanoscience & nanotechnology0104 chemical sciencesOxidative StresschemistryBiochemistryResveratrolLiposomesPhospholipid vesicleBiophysicsMolecular MedicineFemale0210 nano-technology
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Preparation, characterization and in vitro antimicrobial activity of ampicillin-loaded polyethylcyanoacrylate nanoparticles.

1998

In this paper, the experimental conditions for preparing ampicillin-loaded polyethylcyanoacrylate (PECA) nanoparticles are described. The effects of drug concentration and surfactant type in the polymerization medium on the particle size distribution and loading capacity were studied. The results of these studies show that only the type of surfactant has an impact on the nanoparticle dimensions. The release rate of ampicillin from PECA nanoparticles at pH 7.4 (extracellular value pH) performed either with and without esterases, show that the drug release is considerably increased in the presence of these exzymes. The results of drug release study at pH 1.1 (simulated gastric juice) are very…

Materials scienceChemistry PharmaceuticalBiophysicsNanoparticleBioengineeringBiocompatible MaterialsMicrobial Sensitivity TestsPenicillinsPoloxamerBiomaterialsSurface-Active AgentsPulmonary surfactantDrug StabilityExtracellularOrganic chemistryCyanoacrylatesDrug CarriersChromatographyBiomaterialBiodegradationAntimicrobialIn vitroPolymerizationMechanics of MaterialsDelayed-Action PreparationsCeramics and CompositesAmpicillinBiomaterials
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Dispersions of nanosilica in biocompatible copolymers

2010

Dispersions of nanosilica in matrices of biocompatible copolymers were prepared by melt blending. Copolymers with variable molecular size at fixed hydrophilic/hydrophobic ratio and nanosilicas with different interfacial areas were studied. For comparison, a nanoclay was also investigated. The interfacial area played a relevant role in conferring peculiar properties on the nanohybrids. Amazingly, the macromolecule adsorbed on the nanosilica surface maintains some crystallinity which was quantitatively evaluated. In contrast, all the macromolecule anchored to the nanoclay surface is amorphous. The change of the crystalline state was reflected in the dielectric and the electrical conductivity …

Materials scienceNanocompositePolymers and PlasticsPoloxamerCondensed Matter PhysicsMicrostructureAmorphous solidCrystallinityPluronics Nanosilica Laponite RD Crystallinity Morphology Thermal stabilityMechanics of MaterialsMaterials ChemistryCopolymerThermal stabilityComposite materialMacromoleculeSettore CHIM/02 - Chimica Fisica
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Physical characterization of alginate-Pluronic F127 gel for endoluminal NABDs delivery

2014

Here we focus the attention on the physical characteristics of a highly biocompatible hydrogel made up of crosslinked alginate and Pluronic F127 (PF127). This is a composite polymeric blend we propose for artery endoluminal delivery of an emerging class of molecules named nucleic acid based drugs (NABDs). The physical characterization of our composite gel, i.e. mesh size distribution and PF127-alginate mutual organization after crosslinking, can significantly determine the NABDs release kinetics. Thus, to explore these aspects, different technical approaches, i.e. rheology, low/high field NMR and TEM, were used. While rheology provided information at the macroscopic and nano-level, the othe…

Materials sciencegel pavingAlginatesKineticsComposite numberNanotechnologyPoloxamerMicellerestenosisRheologyalginateArterial wallMicellesDrug Carriersgel paving; rheology; NMR; alginate; Pluronic; restenosisGeneral ChemistryPluronicPoloxamerCondensed Matter PhysicsNMRCharacterization (materials science)Chemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSolute diffusionrheologyNABDs release kinetics PF127 alginate gel paved stent artery endoluminal deliveryGels
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