Search results for "Biomaterial"

showing 10 items of 1350 documents

Biotin-Containing Reduced Graphene Oxide-Based Nanosystem as a Multieffect Anticancer Agent: Combining Hyperthermia with Targeted Chemotherapy

2015

Among the relevant properties of graphene derivatives, their ability of acting as an energy-converting device so as to produce heat (i.e., thermoablation and hyperthermia) was more recently taken into account for the treatment of solid tumors. In this pioneering study, for the first time, the in vitro RGO-induced hyperthermia was assessed and combined with the stimuli-sensitive anticancer effect of a biotinylated inulin-doxorubicin conjugate (CJ-PEGBT), hence, getting to a nanosystem endowed with synergic anticancer effects and high specificity. CJ-PEGBT was synthesized by linking pentynoic acid and citraconic acid to inulin. The citraconylamide pendants, used as pH reversible spacer, were …

Polymers and PlasticsBiotinAntineoplastic AgentsBreast NeoplasmsBioengineeringlaw.inventionBiomaterialschemistry.chemical_compoundDrug Delivery SystemslawMaterials ChemistrymedicineHumansMoietyOrganic chemistryDoxorubicinChemistryGrapheneInulinHyperthermia InducedHydrogen-Ion ConcentrationCitraconic acidgraphene drug delivery hypertermia anticancer inulinCombinatorial chemistryDoxorubicinSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiotinylationDrug deliveryMCF-7 CellsNanoparticlesNanomedicineFemaleGraphiteConjugatemedicine.drugBiomacromolecules
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Bioreducible Poly-l-Lysine-Poly[HPMA] Block Copolymers Obtained by RAFT-Polymerization as Efficient Polyplex-Transfection Reagents

2015

Polylysine-b-p[HPMA] block copolymers containing a redox-responsive disulfide bond between both blocks are synthesized by RAFT polymerization of pentafluorphenyl-methacrylate with a macro-CTA from Nϵ-benzyloxycarbonyl (Cbz) protected polylysine (synthesized by NCA polymerization). This polylysine-b-p[PFMA] precursor block copolymer is converted to polylysine(Cbz)-b-p[HPMA] by postpolymerization modification with 2-hydroxypropylamine. After removal of the Cbz protecting group, cationic polylysine-b-p[HPMA] copolymers with a biosplittable disulfide moiety became available, which can be used as polymeric transfection vectors. These disulfide linked polylysine-S-S-b-p[HPMA] block copolymers sho…

Polymers and PlasticsCationic polymerizationBioengineering02 engineering and technologyTransfection010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesBiomaterialschemistry.chemical_compoundchemistryPolymerizationPolylysinePolymer chemistryMaterials ChemistryCopolymerMoietyReversible addition−fragmentation chain-transfer polymerization0210 nano-technologyProtecting groupBiotechnologyMacromolecular Bioscience
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Amphiphilic Copolymers Based on Poly[(hydroxyethyl)-d,l-aspartamide]: A Suitable Functional Coating for Biocompatible Gold Nanostars

2013

Novel amphiphilic copolymers have been synthesized based on a biocompatible poly(hydroxyethylaspartamide) (PHEA) backbone, bearing both anchoring groups for gold nanoparticles, such as thiols and disulfide, and conjugable moieties, such as amino groups, the latter as points suitable for appending further functional agents. The strategy was to functionalize α,β-poly[(N-2- hydroxyethyl)-d,l-aspartamide] (PHEA) with PEG2000-NH2 and with ethylenediamine (EDA) obtaining a partially pegylated copolymer with a large number of pendant primary amino groups. A fraction of the latter was conjugated with molecules bearing terminal thiol moieties such as 12-mercaptododecanoic acid (MDA) and disulfide gr…

Polymers and PlasticsCell SurvivalMetal NanoparticlesBioengineeringEthylenediamineengineering.materialConjugated systemPolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundCoated Materials BiocompatibleCoatingCell Line TumorMaterials TestingAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansMoleculePoly(hydroxyethyl)-DL-aspartamideParticle Sizechemistry.chemical_classificationAmphiphilic copolymersgold nanostarlipoic acidEthylenediamineschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoColloidal goldThiolengineeringGoldPeptidesgold nanoparticleBiomacromolecules
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Polypeptoid-block-polypeptide Copolymers: Synthesis, Characterization, and Application of Amphiphilic Block Copolypept(o)ides in Drug Formulations an…

2013

We report the synthesis of polysarcosine-block-polyglutamic acid benzylester (PSar-block-PGlu(OBn)) and polysarcosine-block-polylysine-ε-N-benzyloxycarbonyl (PSar-block-PLys(Z)) copolymers. The novel polypeptoid-block-polypeptide copolymers (Copolypept(o)ides) have been synthesized by ring-opening polymerization (ROP) of N-carboxyanhydrides (NCAs). Polymerization conditions were optimized regarding protecting groups, block sequence and length. While the degree of polymerization of the PSar block length was set to be around 200 or 400, PGlu(OBn) and PLys(Z) block lengths were varied between 20 to 75. The obtained block copolymers had a total degree of polymerization of 220-475 and dispersity…

Polymers and PlasticsCell SurvivalPolymersSurface PropertiesChemistry PharmaceuticalDispersityBioengineeringDegree of polymerizationBiomaterialsPeptoidsStructure-Activity RelationshipSurface-Active AgentsColloidCell Line TumorBlock (telecommunications)AmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansParticle SizeDose-Response Relationship DrugChemistryMiniemulsionHEK293 CellsPolymerizationEmulsionsPeptidesBiomacromolecules
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Size- and coating-dependent uptake of polymer-coated gold nanoparticles in primary human dermal microvascular endothelial cells.

2012

A library-orientated approach is used to gain understanding of the interactions of well-defined nanoparticles with primary human endothelial cells, which are a key component of the vasculature. Fifteen sequentially modified gold nanoparticles (AuNPs) based on three different core sizes (18, 35, 65 nm) and five polymeric coatings were prepared. The synthetic methodology ensured homogeneity across each series of particles to allow sequential investigation of the chemical features on cellular interactions. The toxicity of these nanoparticles, their uptake behavior in primary human dermal microvascular endothelial cells (HDMECs), and quantification of uptake were all investigated. The results o…

Polymers and PlasticsCell SurvivalPolymersSurface PropertiesNanoparticleMetal NanoparticlesBioengineeringNanotechnologyengineering.materialBiomaterialsCoatingMaterials ChemistryHumansParticle SizeCytotoxicityCells CulturedSkinchemistry.chemical_classificationGlucosamineChemistryEndothelial CellsPolymerEthylenediaminesIn vitroColloidal goldMicrovesselsengineeringBiophysicsGoldBiomacromolecules
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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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α-Mannosyl-Functionalized Cationic Nanohydrogel Particles for Targeted Gene Knockdown in Immunosuppressive Macrophages

2019

Immunosuppressive M2 macrophages govern the immunophathogenic micromilieu in many severe diseases including cancer or fibrosis, thus, their re-polarization through RNA interference is a promising concept to support combinatorial therapies. For targeted siRNA delivery, however, safe and stable carriers are required that manage cell specific transport to M2 macrophages. Here, siRNA-loaded cationic nanogels are reported with α-mannosyl decorated surfaces that target and modify M2 macrophages selectively. Via amphiphilic precursor block copolymers bearing one single α-mannosyl moiety at their chain end mannosylated cationic nanohydrogel particles (ManNP) were obtained of 20 nm diameter determin…

Polymers and PlasticsCellBioengineering02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsMiceFibrosisRNA interferenceCationsmedicineMaterials ChemistryAnimalsHumansMannanImmunosuppression TherapyGene knockdownbiologyChemistryMacrophagesHydrogels3T3 CellsHep G2 Cells021001 nanoscience & nanotechnologymedicine.diseaseIn vitro0104 chemical sciencesCell biologymedicine.anatomical_structureRAW 264.7 CellsConcanavalin AGene Knockdown Techniquesbiology.proteinNanoparticles0210 nano-technologyMannoseMannose receptorBiotechnologyMacromolecular Bioscience
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Effect of Core-Crosslinking on Protein Corona Formation on Polymeric Micelles.

2021

Most nanomaterials acquire a protein corona upon contact with biological fluids. The magnitude of this effect is strongly dependent both on surface and structure of the nanoparticle. To define the contribution of the internal nanoparticle structure, protein corona formation of block copolymer micelles with poly(N-2-hydroxypropylmethacrylamide) (pHPMA) as hydrophilic shell, which are crosslinked-or not-in the hydrophobic core is comparatively analyzed. Both types of micelles are incubated with human blood plasma and separated by asymmetrical flow field-flow fractionation (AF4). Their size is determined by dynamic light scattering and proteins within the micellar fraction are characterized by…

Polymers and PlasticsChemical PhenomenaLightPolymersNanoparticleBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesMicelleMass SpectrometryPolyethylene GlycolsBiomaterialsCorona (optical phenomenon)PlasmaDynamic light scatteringMaterials ChemistryCopolymerHumansScattering RadiationChromatography High Pressure LiquidMicellesGel electrophoresisChemistry021001 nanoscience & nanotechnologyBlood proteins0104 chemical sciencesNanostructuresCross-Linking ReagentsBiophysicsProtein CoronaAdsorption0210 nano-technologyHydrophobic and Hydrophilic InteractionsBiotechnologyMacromolecular bioscience
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Heparin-Based Nanocapsules as Potential Drug Delivery Systems

2015

Herein, the synthesis and characterization of heparin-based nanocapsules (NCs) as potential drug delivery systems is described. For the synthesis of the heparin-based NCs, the versatile method of miniemulsion polymerization at the droplets interface was achieved resulting in narrowly distributed NCs with 180 nm in diameter. Scanning and transmission electron microscopy images showed clearly NC morphology. A highly negative charge density for the heparin-based NCs was determined by measuring the electro-kinetic potential. Measuring the activated clotting time demonstrated the biological intactness of the polymeric shell. The ability of heparin-based NCs to bind to antithrombin (AT III) was i…

Polymers and PlasticsChemistryAnalytical chemistryBioengineeringIsothermal titration calorimetrybehavioral disciplines and activitiesNanocapsulesBiomaterialsMiniemulsionPolymerizationChemical engineeringDynamic light scatteringTransmission electron microscopymental disordersDrug deliveryMaterials ChemistryChemical stabilityBiotechnologyMacromolecular Bioscience
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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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