Search results for "controlled release."

showing 10 items of 132 documents

Biodegradable pH-Sensitive Poly(ethylene glycol) Nanocarriers for Allergen Encapsulation and Controlled Release

2015

In the last decades, the number of allergic patients has increased dramatically. Allergen-specific immunotherapy (SIT) is the only available cause-oriented therapy so far. SIT reduces the allergic symptoms, but also exhibits some disadvantages; that is, it is a long-lasting procedure and severe side effects like anaphylactic shock can occur. In this work, we introduce a method to encapsulate allergens into nanoparticles to avoid severe side effects during SIT. Degradable nanocarriers combine the advantage of providing a physical barrier between the encapsulated cargo and the biological environment as well as responding to certain local stimuli (like pH) to release their cargo. This work int…

Polymers and PlasticsProton Magnetic Resonance SpectroscopyNanoparticleBioengineeringmacromolecular substancesmedicine.disease_causePolyethylene GlycolsBiomaterialschemistry.chemical_compoundAllergenPolymer chemistryPEG ratioMaterials ChemistrymedicineHumansNanotechnologyDrug CarriersAcetalAllergensHydrogen-Ion ConcentrationEndolysosomeControlled releaseCombinatorial chemistrychemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationChromatography GelNanocarriersEthylene glycolBiomacromolecules
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Metallo-Polymer Chain Extension Controls the Morphology and Release Kinetics of Microparticles Composed of Terpyridine-Capped Polylactides and their …

2016

Control over morphology and porosity of supramolecular complexed polylactide (PLA) microparticles can be achieved by manipulation of the supramolecular interactions between their constituent polymeric building blocks. It is expected that such modular systems are ideal candidates to serve as degradable delivery carriers. In view of this goal, this study reports about a modular fabrication of biodegradable microparticles from terpyridine (TPy) and bisterpyridine (bisTPy) end-functionalized PLAs that can be transiently extended by chain association through differently strong complexation to three metal cations: Ni2+ , Co2+ , or Fe2+ . Further influence on the morphology of the particles can be…

Polymers and PlasticsPyridinesSurface PropertiesPolyestersKineticsSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundMaterials ChemistryOrganometallic CompoundsMicroparticleParticle SizePorositychemistry.chemical_classificationMolecular StructureChemistryOrganic ChemistryStereoisomerismPolymer021001 nanoscience & nanotechnologyControlled release0104 chemical sciencesKineticsChemical engineeringParticleTerpyridine0210 nano-technologyMacromolecular rapid communications
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CONTROLLED RELEASE OF IgG BY NOVEL UV INDUCED POLYSACCHARIDE/POLY(AMINO ACID)HYDROGELS

2009

The development of new protein and peptide drugs needs new delivery systems able to entrap such drugs in safe conditions without affecting their structure and biological activity. In this context, the present work reports a new approach to load IgG, used as a model of therapeutic proteins such as anti-TNF-alpha monoclonal antibodies, into a polymeric system able to release the entrapped IgG in a controlled manner. In particular, new polysaccharide/poly(amino acid) UV induced hydrogels are proposed as colon delivery systems for human IgG. The poly(amino acid), alpha,beta-poly[N-(2-hydroxyethyl)-D,L-aspartamide], has been functionalized with methacrylic anhydride, while the polysaccharide, in…

Polymers and PlasticsUltraviolet RaysMethacrylic anhydrideBioengineeringPeptideContext (language use)Enzyme-Linked Immunosorbent AssayBiomaterialschemistry.chemical_compoundCrohn DiseasePolysaccharidesMaterials ChemistryOrganic chemistryHumanshydrogels drug releaseAmino Acidschemistry.chemical_classificationChromatographytechnology industry and agricultureSuccinic anhydrideHydrogelsControlled releaseAmino acidchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDelayed-Action PreparationsImmunoglobulin GSelf-healing hydrogelsChromatography GelCaco-2 CellsDrug carrierBiotechnology
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Core Cross-Linked Polymeric Micelles for Specific Iron Delivery: Inducing Sterile Inflammation in Macrophages.

2021

Iron is an essential co-factor for cellular processes. In the immune system, it can activate macrophages and represents a potential therapeutic for various diseases. To specifically deliver iron to macrophages, iron oxide nanoparticles are embedded in polymeric micelles of reactive polysarcosine-block-poly(S-ethylsulfonyl-l-cysteine). Upon surface functionalization via dihydrolipoic acid, iron oxide cores act as crosslinker themselves and undergo chemoselective disulfide bond formation with the surrounding poly(S-ethylsulfonyl-l-cysteine) block, yielding glutathione-responsive core cross-linked polymeric micelles (CCPMs). When applied to primary murine and human macrophages, these nanoparti…

PolymersIronBiomedical EngineeringMacrophage polarizationIron oxidePharmaceutical Science02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundMiceImmune systemDihydrolipoic acidMacrophageAnimalsMicellesInflammationMacrophages021001 nanoscience & nanotechnologyControlled release0104 chemical scienceschemistryBiophysics0210 nano-technologyIron oxide nanoparticlesIntracellularAdvanced healthcare materials
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Release and permeation profiles of spray-dried chitosan microparticles containing caffeic acid

2018

Made available in DSpace on 2018-12-11T17:17:17Z (GMT). No. of bitstreams: 0 Previous issue date: 2018-03-01 Caffeic acid (CA), a phenolic compound found in plants with antioxidant and antimicrobial activity, induces collagen production and prevents premature aging of the skin. The objective of this study was to develop two types of chitosan microparticles (MP) containing CA and to relate the morphology with the release and permeation profiles. One type of MP was prepared from a hydroalcoholic solution (MPI) and the other from an aqueous solution (MPII). Their morphology and size was evaluated by high-resolution scanning electron microscopy. The release profile of CA was evaluated using the…

Premature agingPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyArticleChitosan03 medical and health scienceschemistry.chemical_compound0302 clinical medicineCaffeic acidChitosan microparticlesControlled releaseCellulosePharmacologyCaffeic acidChromatographyAqueous solutionlcsh:RM1-950PermeationPermeation021001 nanoscience & nanotechnologyControlled releaseMembranelcsh:Therapeutics. PharmacologychemistrySpray-dryer0210 nano-technologySaudi Pharmaceutical Journal
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Caspase 3 Targeted Cargo Delivery in Apoptotic Cells Using Capped Mesoporous Silica Nanoparticles

2015

[EN] Excessive apoptotic cell death is at the origin of several pathologies, such as degenerative disorders, stroke or ischemia-reperfusion damage. In this context, strategies to improve inhibition of apoptosis and other types of cell death are of interest and may represent a pharmacological opportunity for the treatment of cell-death-related disorders. In this scenario new peptide-containing delivery systems (solids S1-P1and S1-P2) are described based on meso-porous silica nanoparticles (MSNs) loaded with a dye and capped with the KKGDEVDKKARDEVDK (P1) peptide that contains two repeats of the DEVD target sequence that are selectively hydrolyzed by caspase3 (C3). This enzyme plays a central…

Programmed cell deathgated mesoporous materialsCaspase 3Context (language use)ApoptosisCatalysisGated mesoporous materialsHeLaQUIMICA ORGANICAQUIMICA ANALITICAmedicineBIOQUIMICA Y BIOLOGIA MOLECULARControlled releaseHumansCisplatinDrug CarriersbiologyChemistryCaspase 3Organic ChemistryQUIMICA INORGANICAGeneral ChemistryMesoporous silicabiology.organism_classificationSilicon DioxideMolecular biologyCell biologycaspase3ApoptosisCytoplasmpeptidesNanoparticlesnanoparticlesCisplatinPeptidescontrolled releasePorositymedicine.drugHeLa Cells
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Quality control of gold nanoparticles as pharmaceutical ingredients

2019

Abstract Nanoparticles are being developed for a wide range of medical applications such as, controlled release, drug delivery systems or imagery, theranostics, implants…. For the moment, there is no legal definition of nanoparticles or nanomaterials for therapeutic use. The specific case of gold nanoparticles is not an exception: their current definition as nanoparticle material does not correspond to classic pharmaceutical ingredients as described in Pharmacopoeias. In this study, more than 30 different batches of citrate stabilized gold nanoparticles (AuNP) were synthesized and analyzed thanks to both classical approaches (UV–Vis spectrophotometry, dynamic light scattering coupled or not…

Quality ControlMaterials sciencePharmaceutical ScienceNanoparticleMetal NanoparticlesNanotechnology02 engineering and technologyAcetates030226 pharmacology & pharmacyCitric AcidNanomaterials03 medical and health sciences0302 clinical medicineCapillary electrophoresisDynamic light scatteringDrug Stability[CHIM.ANAL]Chemical Sciences/Analytical chemistrySpectrophotometrymedicinePolyaminesComputingMilieux_MISCELLANEOUSmedicine.diagnostic_testElectrophoresis Capillary[SDV.SP]Life Sciences [q-bio]/Pharmaceutical sciences021001 nanoscience & nanotechnologyControlled releaseColloidal goldDrug deliveryGold0210 nano-technology
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Controlled release of tyrosol and ferulic acid encapsulated in chitosan–gelatin films after electron beam irradiation

2016

Abstract This work deals with the study of the release kinetics of antioxidants (ferulic acid and tyrosol) incorporated into chitosan–gelatin edible films after irradiation processes. The aim was to determine the influence of electron beam irradiation (at 60 kGy) on the retention of antioxidants in the film, their release in water (pH=7) at 25 °C, in relation with the barrier and mechanical properties of biopolymer films. The film preparation process coupled to the irradiation induced a loss of about 20% of tyrosol but did not affect the ferulic acid content. However, 27% of the ferulic acid remained entrapped in the biopolymer network during the release experiments whereas all tyrosol was …

Radiationfood.ingredientKinetics04 agricultural and veterinary sciencesengineering.material040401 food scienceGelatinControlled releaseChitosanTyrosolFerulic acidchemistry.chemical_compound0404 agricultural biotechnologyfoodchemistryengineeringOrganic chemistryBiopolymerIrradiationNuclear chemistryRadiation Physics and Chemistry
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Enzyme-responsive intracellular-controlled release using silica mesoporous nanoparticles capped with ε-poly-L-lysine.

2014

The synthesis and characterization of two new capped silica mesoporous nanoparticles for controlled delivery purposes are described. Capped hybrid systems consist of MCM-41 nanoparticles functionalized on the outer surface with polymer epsilon-poly-L-lysine by two different anchoring strategies. In both cases, nanoparticles were loaded with model dye molecule [Ru(bipy)(3)](2+). An anchoring strategy involved the random formation of urea bonds by the treatment of propyl isocyanate-functionalized MCM-41 nanoparticles with the lysine amino groups located on the epsilon-poly-L-lysine backbone (solid Ru-rLys-S1). The second strategy involved a specific attachment through the carboxyl terminus of…

Silicon dioxideNanoparticlemesoporous materialsCatalysisRutheniumchemistry.chemical_compoundHydrolysisQUIMICA ORGANICACell Line TumorQUIMICA ANALITICAOrganic chemistryHumansPolylysineColoring Agentschemistry.chemical_classificationintracellular releaseOrganic ChemistryQUIMICA INORGANICAGeneral ChemistryPolymerMesoporous silicaSilicon DioxideControlled releaseCombinatorial chemistrychemistryPolylysineDelayed-Action Preparationsanchoring strategyNanoparticlesnanoparticlesMesoporous materialLysosomesPorositypoly-L-lysineHeLa CellsChemistry (Weinheim an der Bergstrasse, Germany)
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Protein delivery based on uncoated and chitosan-coated mesoporous silicon microparticles

2011

Mesoporous silicon is a biocompatible, biodegradable material that is receiving increased attention for pharmaceutical applications due to its extensive specific surface. This feature enables to load a variety of drugs in mesoporous silicon devices by simple adsorption-based procedures. In this work, we have addressed the fabrication and characterization of two new mesoporous silicon devices prepared by electrochemistry and intended for protein delivery, namely: (i) mesoporous silicon microparticles and (ii) chitosan-coated mesoporous silicon microparticles. Both carriers were investigated for their capacity to load a therapeutic protein (insulin) and a model antigen (bovine serum albumin) …

SiliconMaterials scienceSiliconBSAchemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistryPorous silicon01 natural sciencesChitosanchemistry.chemical_compoundDrug Delivery SystemsColloid and Surface ChemistryAdsorptionPorous siliconElectrochemistryAnimalsInsulinPhysical and Theoretical ChemistryBovine serum albuminChitosanbiologyProteintechnology industry and agricultureProteinsSerum Albumin BovineSurfaces and InterfacesGeneral Medicine021001 nanoscience & nanotechnologyequipment and suppliesControlled release0104 chemical sciencesMesoporous organosilicachemistryMicroscopy Electron Scanningbiology.proteinElectrochemical pore formationCattle:Investigación::33 Ciencias tecnológicas::3312 Tecnología de materiales [Materias]0210 nano-technologyMesoporous materialBiotechnology
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