Search results for "Ligo"

showing 10 items of 1427 documents

Size-dependent knockdown potential of siRNA-loaded cationic nanohydrogel particles.

2014

To overcome the poor pharmacokinetic conditions of short double-stranded RNA molecules in RNA interference therapies, cationic nanohydrogel particles can be considered as alternative safe and stable carriers for oligonucleotide delivery. For understanding key parameters during this process, two different types of well-defined cationic nanohydrogel particles were synthesized, which provided nearly identical physicochemical properties with regards to their material composition and resulting siRNA loading characteristics. Yet, according to the manufacturing process using amphiphilic reactive ester block copolymers of pentafluorophenyl methacrylate (PFPMA) and tri(ethylene glycol)methyl ether m…

Polymers and PlasticsNanogelsBioengineeringEtherMethacrylateProtein Structure SecondaryPolyethylene GlycolsBiomaterialschemistry.chemical_compoundCationsAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansPolyethyleneimineParticle SizeRNA Small InterferingRNA Double-StrandedOligonucleotideCationic polymerizationHydrogelschemistryChemical engineeringGene Knockdown TechniquesEthylene glycolNanogelHeLa CellsBiomacromolecules
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Spectroscopic Studies of Oligonucleotide Adducts and Base Sequence Preference of Adducts Formed by the Stereoisomers of 7,8-Dihydroxy-9,10-epoxy-7,8,…

1996

Abstract 5′-d(CCTATAGATATCC) has been reacted with BPDE and the adducts derived from binding of BPDE to the exocyclic amino group of deoxyguanosine (dG) were studied with spectroscopic methods. The major dG-adducts of (+)- and (-)-anti-BPDE and a minor adduct of (+)-syn-BPDE showed the characteristics of trans-adducts. The major products formed with (+)- and (-)-syn-BPDE exhibit cis-adduct characteristics. Annealing of BPDE-modified oligonucleotides to complementary or partially complementary strands results in reduced fluorescence intensity in several cases and in others the intensity is markedly increased. These differences demonstrate that the adduct microenvironment is strongly influenc…

Polymers and PlasticsOligonucleotideStereochemistryOrganic ChemistryEpoxyPhotochemistryAdductchemistry.chemical_compoundchemistryDuplex (building)visual_artpolycyclic compoundsMaterials Chemistryvisual_art.visual_art_mediumPyreneDeoxyguanosineThermal stabilityBase sequencePolycyclic Aromatic Compounds
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Branched versus linear oligo(dimethylsiloxane): Differences in their thermodynamic interaction with solvents

2010

The thermodynamic behavior of linear and of branched oligo(dimethylsiloxane) (O-DMS) solutions was studied by means of vapor pressure measurements and vapor pressure osmometry at different temperatures for the thermodynamically favorable solvent THF. The branched material required for that purpose was synthesized and afterwards fractionated by means of the single solvent acetone to eliminate components of low degrees of branching. The Flory-Huggins interaction parameters, χ, for the systems THF/O-DMS as a function of composition pass a minimum at all temperatures (25, 40, and 60 °C) in the case of the branched material. For the unbranched oligomer such a minimum is only observed at 60 °C. A…

Polymers and PlasticsVapor pressureVapor pressure osmometryFractionationCondensed Matter PhysicsBranching (polymer chemistry)OligomerDilutionSolventchemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryAcetonePhysical chemistryPhysical and Theoretical ChemistryJournal of Polymer Science Part B: Polymer Physics
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Enzymatically catalyzed synthesis of photocrosslinkable oligophenols

2000

The HRP-catalyzed oligomerization of cinnamoyl-hydroquinone-ester and cinnamoyl-4-hydroxyanilide led to the formation of soluble polyphenols. The oligomers were synthexized in water/1,4-dioxane and in water/acetone mixtures and characterized by NMR, FTIR and SEC. Upon UV treatment of the homogenoes films the polyphenols were crosslinked due to [2+2]-cycloadditions of the cinnamoyl functions.

Polymers and PlasticsbiologyOrganic ChemistryCondensed Matter PhysicsOligomerCatalysisEnzyme catalysischemistry.chemical_compoundchemistryPhotosensitivityPolyphenolPolymer chemistryMaterials ChemistryAcetonebiology.proteinOrganic chemistryPhenolsPhysical and Theoretical ChemistryPeroxidaseMacromolecular Chemistry and Physics
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The Formation of Glycerol Oligomers with Two New Types of End Groups in the Presence of a Homogeneous Alkaline Catalyst

2019

The purpose of this work was to synthesize and characterize oligoglycerols with the chains of more than four repeating units. Those oligoglycerols may have some interesting applications, among others, as polyoxyalkylation starters. The glycerol oligomerization process was carried out during 12 h, at 230 &deg

Polymers and PlasticscatalysisElectrospray ionizationmechanismGeneral ChemistryglycerolCarbon-13 NMRArticleCatalysisoligomerizationlcsh:QD241-441chemistry.chemical_compoundchemistrylcsh:Organic chemistryPolymer chemistryGlycerololigoglycerolCarboxylateFourier transform infrared spectroscopySodium carbonatepolyglycerolsBar (unit)Polymers
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Cellular Uptake of DNA Block Copolymer Micelles with Different Shapes

2008

The cellular uptake of DNA block copolymer micelles composed of DNA-b-PPO in Caco-2 cells was studied. In particular it was investigated if the shape of micelle aggregates influences the internalization. Rod-like polymeric particles were taken up 12 times more efficiently than their spherical counter parts although they were composed of the same constituents. Furthermore, it was observed that internalization of all the micelle systems was more efficient than the pristine DNA controls. A cytotoxicity assay proved the non-toxic nature of DNA-b-PPO micelle aggregates.

Polymers and PlasticsmicellesOligonucleotidemedia_common.quotation_subjectOrganic Chemistrycellular uptakeNanoparticleCaco-2DNAMicellechemistry.chemical_compoundchemistryCritical micelle concentrationMaterials ChemistryBiophysicsCopolymerOrganic chemistrynanoparticlesamphiphilic polymerInternalizationDrug carrierhybridizationDNAmedia_commonMacromolecular Rapid Communications
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Torsional effects on the molecular polarizabilities of the benzothiazole (A)-benzobisthiazole (B) oligomer A-B13-A

1996

Abstract We outline a method for the calculation of multipole moments and molecular dipole-dipole ( ), dipole-quadrupole ( ), and quadrupole-quadrupole ( ) polarizabilities, which we have successfully applied to benzothiazole (A)-benzobisthiazole (B) oligomer A-B13-A. Three model rotational isomers have been characterized: (1) the fully planar (000) rotational isomer; (2) a conformation with each unit rotated 10° in the alternate direction (+−+), and (3) a rotational isomer with each unit rotated 10° in the same direction (+++). The dipole moment, μ , is smaller for isomers 000 and +−+ than for isomer +++. The calculation of , , and has been performed by use of the interacting induced dipol…

PolymersChemistryStatic ElectricityMolecular ConformationBiophysicsBiochemistryOligomerThiazolesCrystallographychemistry.chemical_compoundDipoleModels ChemicalSolubilityBenzothiazoleComputational chemistryComputer GraphicsPhysics::Atomic and Molecular ClustersPolarComputer SimulationBenzothiazolesPhysics::Chemical PhysicsSolubilityAnisotropyMultipole expansionOrder of magnitudeJournal of Molecular Graphics
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Learning from nature: beta-sheet-mimicking copolymers get organized.

2007

The solution structures formed by coil-coil copolymers arise from the selective solvation of one of the two blocks and have been well described. In most cases in such relatively simple synthetic structures there are no specific attractive forces that can aid the aggregation process. Nature, however, provides plenty of inspiring polymeric architectures that are shaped and ordered hierarchically by noncovalent forces. The high level of structural definition displayed by proteins, for example, is unmatched by synthetic polymers. An emerging area of interest in polymer science tries to combine the best of both worlds, the natural and the synthetic, by conjugating synthetic polymers and beta-she…

PolymersSupramolecular chemistryBeta sheetNanotechnologyMicroscopy Atomic ForceProtein EngineeringCatalysisProtein Structure SecondaryPolyethylene GlycolsMicroscopy Electron TransmissionCopolymerchemistry.chemical_classificationIntermolecular forceSolvationProteinsGeneral ChemistryPolymerSolution structureProtein Structure TertiarySupramolecular polymersChemistrychemistryModels ChemicalNanoparticlesPeptidesOligopeptidesAngewandte Chemie (International ed. in English)
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Structure of isotactic polypropylene/ hydrogenated oligo(cyclopentadiene) blends: 1. Polypropylene-rich blends

1998

Blends of isotactic polypropylene (iPP) and hydrogenated oligo(cyclopentadiene) (HOCP) containing 30% or less HOCP have been studied by small-angle X-ray scattering in the temperature range 25 to 160°C. The structure of blends has been analysed in terms of a pseudo two-phase model consisting of stacks of lamellae whose thickness is a function of temperature and composition. Structural parameters of the model have been derived and their temperature and composition dependences have been interpreted in the light of existing theories.

PolypropyleneMaterials scienceCyclopentadienePolymers and PlasticsSmall-angle X-ray scatteringOrganic ChemistryAtmospheric temperature rangeOligomerchemistry.chemical_compoundchemistryChemical engineeringTacticityPolymer chemistryMaterials ChemistryLamellar structurePolymer blendPolymer
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Study of thermal properties of polyethylene and polypropylene nanocomposites with long alkyl chain-substituted POSS fillers

2016

The effect of incorporation of octakis({alkyl}dimethylsiloxy)octasilsesquioxanes molecules with n-octyl, n-octadecyl and 4-methyl-hexyl substituents on thermal properties of polypropylene (PP), low-density polyethylene (LDPE) and high-density polyethylene (HDPE) was investigated. Thermal properties of those composite materials were evaluated by means of the differential scanning calorimetry (DSC) and thermogravimetric analysis (TG) methods. The type and mass% content of POSS nanofillers influenced the crystallization and melting properties as well as thermal stability of the obtained polyolefin nanocomposites. The incorporated POSS particles—acting as nucleating agents—improved the crystall…

PolypropyleneThermogravimetric analysisMaterials sciencethermal propertiesnucleating agentspolyhedral oligomeric silsesquioxanes02 engineering and technologyPolyethylene010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesthermal stability0104 chemical sciencesPolyolefinchemistry.chemical_compoundLow-density polyethyleneDifferential scanning calorimetrychemistryThermal stabilityHigh-density polyethylenepolyolefin matrix (nano)compositesComposite materialPhysical and Theoretical Chemistry0210 nano-technologyJournal of Thermal Analysis and Calorimetry
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