Search results for "DRUG DELIVERY SYSTEMS"

showing 10 items of 304 documents

Supramolecular Assemblies Based on Complexes of Nonionic Amphiphilic Cyclodextrins and a meso-Tetra(4- sulfonatophenyl)porphine Tributyltin(IV) Deriv…

2013

Amphiphilic cyclodextrin (ACyD) provides water-soluble and adaptable nanovectors by modulating the balance between the hydrophobic and hydrophilic chains at both CyD sides. This work aimed to design nanoassemblies based on nonionic and hydrophilic ACyD (SC6OH) for the delivery of a poor-water-soluble organotin(IV)-porphyrin derivative [(Bu3Sn)4TPPS] to melanoma cancer cells. To characterize the porphyrin derivatives under simulated physiological conditions, a speciation was performed using complementary techniques. In aqueous solution (≤ 20 μM), (Bu3Sn)4TPPS primarily exists as a monomer (2 in Figure 1), as suggested by the low static anisotropy (ρ ≈ 0.02) with a negligible formation of por…

Polymers and PlasticsCell SurvivalSurface PropertiesPotentiometric titrationSupramolecular chemistryAntineoplastic AgentsBioengineeringBiomaterialsStructure-Activity RelationshipSurface-Active Agentschemistry.chemical_compoundDrug Delivery SystemsAmphiphilePolymer chemistryTumor Cells CulturedMaterials ChemistryHumansOrganic chemistryParticle SizeMelanomaMELANOMA porphyrins organotin(IV)Cell Proliferationchemistry.chemical_classificationCyclodextrinsAqueous solutionCell DeathDose-Response Relationship DrugMolecular StructureCyclodextrinPorphyrinNanomedicineMonomerchemistrySettore CHIM/03 - Chimica Generale E InorganicaDrug Screening Assays AntitumorTrialkyltin CompoundsDrug carrier
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From Polymers to Functional Biomaterials.

2017

Polymers and PlasticsChemistryPolymersMEDLINEBioengineeringBiocompatible Materials02 engineering and technologyComputational biology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesModels Biological0104 chemical sciencesBiomaterialsDrug Delivery SystemsMaterials ChemistryAnimalsHumansNanoparticlesRNA Interference0210 nano-technologyBiotechnologyIntroductory Journal ArticleMacromolecular bioscience
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Polypept(o)ides: Hybrid Systems Based on Polypeptides and Polypeptoids.

2015

Polypept(o)ides combine the multifunctionality and intrinsic stimuli-responsiveness of synthetic polypeptides with the "stealth"-like properties of the polypeptoid polysarcosine (poly(N-methyl glycine)). This class of block copolymers can be synthesized by sequential ring opening polymerization of α-amino acid N-carboxy-anhydrides (NCAs) and correspondingly of the N-substituted glycine N-carboxyanhydride (NNCA). The resulting block copolymers are characterized by Poisson-like molecular weight distributions, full end group integrity, and dispersities below 1.2. While polysarcosine may be able to tackle the currently arising issues regarding the gold standard PEG, including storage diseases i…

Polymers and PlasticsChemistryPolysarcosineOrganic ChemistryGene Transfer TechniquesSarcosineCombinatorial chemistryRing-opening polymerizationProtein Structure SecondaryAnhydridesPolymerizationMolecular WeightEnd-groupPeptoidsDrug Delivery SystemsNanomedicineHybrid systemMaterials ChemistryCopolymerNanomedicineHumansAmino AcidsPeptidesProtein secondary structureMacromolecular rapid communications
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Partially Quarternized Amino Functional Poly(methacrylate) Terpolymers: Versatile Drug Permeability Modifiers

2011

Partially quarternized poly(methacrylate) terpolymers (Q-BBMCs) have been synthesized, based on the basic butylated methacrylate copolymer (BBMC/EUDRAGIT E), an excipient approved by the Food and Drug Administration (FDA) and to date mainly applied for tablet coatings. Via straightforward polymer modification reactions, a series of Q-BBMCs with quarternization degrees of 22%, 42%, and 65% has been prepared. Apical to basolateral transport across Caco-2 cell monolayers was investigated, employing the paracellular transported compounds trospium and mannitol. At pH 6.5 quarternization resulted in increased permeation enhancement up to 2.8-fold compared to BBMC, that is, up to 7.3-fold compared…

Polymers and PlasticsExcipientBioengineeringMethacrylatePermeabilityBiomaterialsDrug Delivery SystemsPolymethacrylic AcidsMaterials TestingPolymer chemistryMaterials ChemistryCopolymermedicineHumansTissue Distributionchemistry.chemical_classificationChemistryChemical modificationPolymerHydrogen-Ion ConcentrationPermeationParacellular transportMannitolCaco-2 CellsTabletsmedicine.drugBiomacromolecules
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Enhanced in vivo targeting of murine nonparenchymal liver cells with monophosphoryl lipid A functionalized microcapsules.

2014

A broad spectrum of infectious liver diseases emphasizes the need of microparticles for targeted delivery of immunomodulatory substances to the liver. Microcapsules (MCs) are particularly attractive for innovative drug and vaccine formulations, enabling the combination of antigen, drugs, and adjuvants. The present study aimed to develop microcapsules characterized by an enhanced liver deposition and accelerated uptake by nonparenchymal liver cells (NPCs). Initially, two formulations of biodegradable microcapsules were synthesized from either hydroxyethyl starch (HES) or mannose. Notably, HES-MCs accumulated primarily in the liver, while mannose particles displayed a lung preference. Functio…

Polymers and PlasticsLiver cytologyKupffer CellsMonophosphoryl Lipid AMannoseBioengineeringCapsulesReceptors Cell SurfacePharmacologyBiomaterialsMinor Histocompatibility Antigenschemistry.chemical_compoundInterferon-gammaMiceImmune systemDrug Delivery SystemsAntigenPhagocytosisIn vivoAntigens CDMaterials ChemistryAnimalsSecretionLectins C-TypeCD40 AntigensInterleukin-6Tumor Necrosis Factor-alphaLiver DiseasesDendritic CellsIn vitroMice Inbred C57BLToll-Like Receptor 4Lipid AchemistryBiochemistryLiverNanoparticlesFemaleBiomacromolecules
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Functionalization of Active Ester-Based Polymersomes for Enhanced Cell Uptake and Stimuli-Responsive Cargo Release

2016

Poly(2,3-dihydroxypropyl methacrylamide) (P(DHPMA))-based amphiphilic block copolymers have recently proven to form polymer vesicles (polymersomes). In this work, we further expand their potential by incorporating (i) units for pH-dependent disintegration into the hydrophobic membrane and (ii) mannose as targeting unit into the hydrophilic block. This last step relies on the use of an active ester prepolymer. We confirm the stability of the polymersomes against detergents like Triton X-100 and their low cytotoxicity. The incorporation of 2-(2,2-dimethyl-1,3-dioxolane-4-yl)ethyl methacrylate into the hydrophobic block (lauryl methacrylate) allows a pH-responsive disintegration for cargo rele…

Polymers and PlasticsOctoxynolPolymersMannoseBioengineering02 engineering and technology010402 general chemistryMethacrylate01 natural sciencesBiomaterialschemistry.chemical_compoundDrug Delivery SystemsAmphiphilePolymer chemistryMaterials ChemistryHumansMethacrylamidePrepolymerChemistryVesicleDioxolanesEstersHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesMembranePolymersomeBiophysicsMethacrylates0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiomacromolecules
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in vitro biological evaluation of folate-functionalized block copolymer micelles for selective anti-cancer drug delivery.

2008

The main objective of this study was to evaluate the ability of folic acid-functionalized diblock copolymer micelles to improve the delivery and uptake of two poorly water-soluble anti-tumor drugs, tamoxifen and paclitaxel, to cancer cells through folate receptor targeting. The diblock copolymer used in this study comprised a hydrophilic poly[2-(methacryloyloxy)ethyl phosphorylcholine] (MPC) block, carrying at the chain end the folate targeting moiety, and a pH-sensitive hydrophobic poly[2-(diisopropylamino)ethyl methacrylate] (DPA) block (FA-MPC-DPA). The drug-loading capacities of tamoxifen- and paclitaxel-loaded micelles were determined by high performance liquid chromatography and the m…

Polymers and PlasticsPaclitaxelPhosphorylcholineBioengineeringMicelleBiomaterialsDrug Delivery SystemsFolic AcidPolymethacrylic AcidsPolymer chemistryBLOCK COPOLYMERS MICELLES DRUG DELIVERYMaterials ChemistryHumansCytotoxicityMicellesPhosphorylcholineChemistryAntineoplastic Agents PhytogenicEnd-groupTamoxifenSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoFolate receptorCancer cellBiophysicsCaco-2 CellsDrug carrierK562 CellsFolate targetingBiotechnologyMacromolecular bioscience
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Ionic Hydrogel Based on Chitosan Cross-Linked with 6-Phosphogluconic Trisodium Salt as a Drug Delivery System.

2018

[EN] In this work, 6-phosphogluconic trisodium salt (6-PG(-)Na(+)) is introduced as a new aqueous and nontoxic cross-linking agent to obtain ionic hydrogels. Here, it is shown the formation of hydrogels based on chitosan cross-linked with 6-PG(-)Na(+). This formulation is obtained by ionic interaction of cationic groups of polymer with anionic groups of the cross linker. These hydrogels are nontoxic, do not cause dermal irritation, are easy to extend, and have an adequate adhesion force to be applied as polymeric film over the skin. This AWN formulation exhibits a first order release kinetic and can be applied as drug vehicle for topical administration or as wound dressing for wound healing…

Polymers and PlasticsPolymersAdministration TopicalIonic bondingSalt (chemistry)Bioengineering02 engineering and technology010402 general chemistry01 natural sciencesGluconatesHydrogel Polyethylene Glycol DimethacrylateBiomaterialsChitosanchemistry.chemical_compoundQUIMICA ORGANICADrug Delivery SystemsMaterials ChemistryHumanschemistry.chemical_classificationChitosanWound HealingAqueous solutionWound Closure TechniquesSodiumCationic polymerization021001 nanoscience & nanotechnology0104 chemical sciencesDrug vehicleKineticsCross-Linking ReagentsChemical engineeringchemistrySelf-healing hydrogelsDrug delivery0210 nano-technologyBiomacromolecules
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Aggregation behavior of amphiphilic p(HPMA)-co-p(LMA) copolymers studied by FCS and EPR spectroscopy.

2012

A combined study of fluorescence correlation spectroscopy and electron paramagnetic resonance spectroscopy gave a unique picture of p(HPMA)-co-p(LMA) copolymers in aqueous solutions, ranging from the size of micelles and aggregates to the composition of the interior of these self-assembled systems. P(HPMA)-co-p(LMA) copolymers have shown high potential as brain drug delivery systems, and a detailed study of their physicochemical properties can help to elucidate their mechanism of action. Applying two complementary techniques, we found that the self-assembly behavior as well as the strength of hydrophobic attraction of the amphiphilic copolymers can be tuned by the hydrophobic LMA content or…

Polymers and PlasticsPolymersBioengineeringFluorescence correlation spectroscopyMicelleModels Biologicallaw.inventionBiomaterialsSurface-Active AgentsDrug Delivery SystemslawPolymer chemistryAmphiphileMaterials ChemistrySide chainCopolymerElectron paramagnetic resonanceAlkylMicelleschemistry.chemical_classificationChemistryElectron Spin Resonance SpectroscopyDomperidoneHydrophobeSpectrometry FluorescenceLiposomesMethacrylatesHydrophobic and Hydrophilic InteractionsBiomacromolecules
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Prospective Cancer Therapies Using Stimuli‐Responsive DNA Nanostructures

2021

Financial support by the Emil Aaltonen Foundation, the Sigrid Jusélius Foundation, the Magnus Ehrnrooth Foundation, Academy of Finland (grants no. 317042 and 331151), the Jane and Aatos Erkko Foundation and the Vilho, Yrjö and Kalle Väisälä Foundation of the Finnish Academy of Science and Letters is gratefully acknowledged Nanostructures based on DNA self-assembly present an innovative way to address the increasing need for target-specific delivery of therapeutic molecules. Currently, most of the chemotherapeutics being used in clinical practice have undesired and exceedingly high off-target toxicity. This is a challenge in particular for small molecules, and hence, developing robust and ef…

Polymers and PlasticsStimuli responsiveComputer scienceAptameraptamersBioengineeringNanotechnologyAntineoplastic Agents02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsDrug Delivery Systemsstimuli-based drug deliveryDna nanostructuresNeoplasmsDNA nanotechnologyMaterials ChemistryDNA origamiHumansDNA nanotechnologyimmunostimulationchemotherapeuticsfungiDNA021001 nanoscience & nanotechnologyBiocompatible materialSmall molecule3. Good health0104 chemical sciencesNanostructuresDrug deliveryDNA origami0210 nano-technologyBiotechnology
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