Search results for "Macromolecular Substance"

showing 10 items of 882 documents

Recent advances on application of peptide nucleic acids as a bioreceptor in biosensors development

2019

Abstract The analogs of DNA are unique biomedical tools that are broadly utilized to develop different types of biosensors. Peptide nucleic acids (PNA) are an individual and notable class of nucleic acid analogs due to their unique, novel physicochemical and biochemical characteristics, stability and resistance to nuclease and protease enzymes, significant interactions with complementary strands and remarkable hybridization attributes. Therefore, they are employed in the preparation and fabrication of various types of functional biosensors. In other words, immobilization of PNA as an appropriate diagnostic probe on the surface of electrochemical and optical converters lead to the fabricatio…

chemistry.chemical_classificationNucleaseProteasePeptide nucleic acidbiologymedicine.medical_treatment010401 analytical chemistrytechnology industry and agricultureRNAPeptidemacromolecular substances01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryBiochemistrymedicinebiology.proteinNucleic acidBiosensorSpectroscopyDNATrAC Trends in Analytical Chemistry
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Determining the selective impregnation of waterlogged archaeological woods with poly(ethylene) glycols mixtures by differential scanning calorimetry

2012

The differential scanning calorimetry (DSC) technique was demonstrated to be a reliable and fast tool for the investigation of the selective impregnation of archaeological woods with poly(ethylene) glycols (PEGs) mixtures. To this aim, waterlogged archaeological woods were impregnated by using aqueous mixtures of PEG 4000 and PEG 400 as well as mixtures of these polymers in the melt state. The efficiency of the treatments was also estimated by determining the total consolidant content entrapped into the cavities of degraded wood by means of DSC and thermogravimetry.

chemistry.chemical_classificationPEG 400EthyleneMaterials scienceAqueous solutiontechnology industry and agriculturemacromolecular substancesPolymerCondensed Matter PhysicsArchaeologyThermogravimetryCultural Heritage Woodchemistry.chemical_compoundDifferential scanning calorimetrychemistryPEG ratioPhysical and Theoretical ChemistryPoly ethyleneSettore CHIM/02 - Chimica Fisica
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Supramolecular Thermotropic Liquid Crystalline Materials with Nematic Mesophase Based on Methylated Hyperbranched Polyethylenimine and Mesogenic Carb…

2006

Supramolecular interaction of fully methylated hyperbranched polyethylenimines (PEI) with a mesogen-based carboxylic acid, 5-(p-cyanobiphenoxy)pentanoic acid, results in the formation of supramolecular complexes exhibiting thermotropic liquid crystalline (LC) mesophases. In contrast to the common smectic mesophases of most dendritic LC polymers, nematic LC phase were observed. The complexation of PEI and the mesogen units is due to electrostatic interaction between the carboxylate groups and the ammonium end groups of PEI. LC properties were investigated by a combination of differential scanning calorimetry, polarizing light optical microscopy, and X-ray diffractometry.

chemistry.chemical_classificationPolyethylenimineMaterials sciencePolymers and PlasticsMesogenCarboxylic acidOrganic Chemistrytechnology industry and agricultureSupramolecular chemistryMesophasemacromolecular substancesThermotropic crystalchemistry.chemical_compoundchemistryLiquid crystalPolymer chemistryMaterials ChemistryCarboxylateMacromolecular Rapid Communications
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Supramolecular Nanocycles Comprisingβ-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

2010

We applied 1,3-dipolar cycloaddition to bind ethynylferrocene onto 6I-azido-6I-deoxycyclomaltoheptaose under microwave assisted conditions. The process was investigated by (1) H NMR, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The ability of the synthesized compound to self-organize to cyclic supramolecular structures was investigated by dynamic light scattering measurements and cryo-transmission electron microscopy.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistrymacromolecular substancesCycloadditionInclusion compoundchemistry.chemical_compoundchemistryFerrocenePolymer chemistry13-Dipolar cycloadditionMaterials ChemistryProton NMROrganic chemistryMetalloceneMacromolecular Rapid Communications
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Synthesis, characterisation and properties of α,β-poly(N-2-hydroxyethyl)-dl-aspartamide-graft-maleic anhydride precursors and their stimuli-responsiv…

2009

Abstract A family of poly(amino acid)-maleic anhydride hydrogels were designed and synthesized. Water soluble polymeric precursors were prepared by partially substituting the hydroxyl groups of the α,β-poly( N -2-hydroxyethyl)- dl -aspartamide backbone with maleic anhydride, so as to provide double bonds for crosslinking and carboxylic acid groups for pH and electric field responsiveness. Reaction conditions (reactive mixture composition and catalysis) were systematically varied in order to obtain PHEA–MA precursors with different and reliable graft-maleic anhydride levels. PHEA–MA precursors were characterised by titration, Nuclear Magnetic Resonance ( 1 H NMR), Fourier-Transformed Infrare…

chemistry.chemical_classificationPolymers and PlasticsGeneral Chemical EngineeringCarboxylic acidSize-exclusion chromatographyResponsive hydrogeltechnology industry and agricultureMaleic anhydrideChemical modificationAcid–base titrationGamma irradiationmacromolecular substancesGeneral ChemistryBiochemistryPolyelectrolytechemistry.chemical_compoundchemistryPolymer synthesiSelf-healing hydrogelsPolymer chemistryMaterials ChemistryEnvironmental ChemistryRadical initiatorSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSwellingReactive and Functional Polymers
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Comparison of living polymerization systems

1994

Recent developments in the field of living polymerization are surveyed. Comparison of the available mechanistic and kinetic information is made for living anionic, cationic, free radical, group transfer, ring-opening metathesis, Ziegler-Natta and immortal polymerizations. This evaluation indicates that the majority of living polymerizations involve quasiliving equilibrium between active (propagating) and dormant (nonpropagating) polymer chains. On the basis of the kinetics of a general model for quasiliving and ideal living polymerizations it is concluded that ideal living polymerization is a special subclass of quasiliving polymerizations. Classification of living polymerization systems is…

chemistry.chemical_classificationPolymers and PlasticsKinetic informationOrganic Chemistrytechnology industry and agricultureCationic polymerizationmacromolecular substancesPolymerCondensed Matter PhysicsMetathesisLiving free-radical polymerizationchemistryPolymer chemistryMaterials ChemistryLiving polymerizationReversible addition−fragmentation chain-transfer polymerizationMacromolecular Symposia
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Synthesis and characterization of water-swellable?,?-polyasparthydrazide derivatives

1995

α, β-polyasparthydrazide (PAHy) was crosslinked by glutaraldehyde to form water-swellable materials possessing a three-dimensional molecular network. Different crosslinking degrees were prepared varying glutaraldehyde/PAHy ratio and samples containing 5-fluorouracil were obtained by incorporating the drug into the polymer networks during the crosslinking reaction. All samples were characterized by swelling tests, thermal, x-ray and SEM analysis. Their microstructure was observed through scanning electron microscopy. Furthermore, for samples containing the anticancer drug,in vitro release studies were performed in pH 7.4 buffer solution.

chemistry.chemical_classificationPolymers and PlasticsScanning electron microscopetechnology industry and agriculturemacromolecular substancesPolymerBuffer solutionMicrostructureIn vitrochemistry.chemical_compoundColloid and Surface ChemistrychemistrySelf-healing hydrogelsMaterials ChemistrymedicineGlutaraldehydePhysical and Theoretical ChemistrySwellingmedicine.symptomNuclear chemistryColloid & Polymer Science
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Aqueous Laponite Clay Dispersions in the Presence of Poly(ethylene oxide) or Poly(propylene oxide) Oligomers and their Triblock Copolymers

2008

The effect of polyethylene oxide (PEO) or polypropylene oxide (PPO) oligomers of various molecular weight (Mw) as well as of triblock copolymers, based on PEO and PPO blocks, on aqueous laponite RD suspensions was studied with small-angle neutron scattering (SANS). The radius of gyration (RG) increases for low Mw whereas the opposite occurs for larger Mw. This behavior is explained on the-basis that an effective RG is given by two contributions: (1) the size of the particles coated with the polymer and (2) the interactions between the laponite RD particles which are attractive for small and repulsive for large polymers. The SANS curves in the whole Q-range are well described by a model of n…

chemistry.chemical_classificationPolypropylenePoly(propylene oxide)Materials scienceAqueous solutiontechnology industry and agricultureOxidemacromolecular substancesPolymerSurfaces Coatings and Filmschemistry.chemical_compoundViscositychemistryPolymer chemistryMaterials ChemistryCopolymerLaponite gels polymer SANS viscosityPhysical and Theoretical ChemistryPoly ethylene
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2015

The rationale of the study was two-fold: (i) develop a functional synthetic model of the Cytochrome c oxidase (CcO) active site, (ii) use it as a convenient tool to understand or predict the outcome of the reaction of CcO with ligands (physiologically relevant gases and other ligands). At physiological pH and potential, the model catalyzes the 4-electron reduction of oxygen. This model was immobilized on self-assembled-monolayer (SAM) modified electrode. During catalytic oxygen reduction, electron delivery through SAMs is rate limiting, similar to the situation in CcO. This model contains all three redox-active components in CcO's active site, which are required to minimize the production o…

chemistry.chemical_classificationReactive oxygen speciesbiologyPhysiologySuperoxideActive sitechemistry.chemical_elementmacromolecular substancesOxygenchemistry.chemical_compoundchemistryBiochemistryPhysiology (medical)biology.proteinBiophysicsImidazoleCytochrome c oxidaseHemePeroxynitriteFrontiers in Physiology
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Cyclodextrins in Polymer Synthesis:  Free Radical Polymerization of a N-Methacryloyl-11-aminoundecanoic Acid/β-Cyclodextrin Pseudorotaxane in an Aque…

1999

The relatively hydrophobic monomer N-methacryloyl-11-aminoundecanoic acid (1) was incorporated as a guest into the cavity of β-cyclodextrin (β-CD) as a host, yielding the water-soluble monomer N-me...

chemistry.chemical_classificationRotaxanePolymers and PlasticsAqueous mediumCyclodextrinOrganic ChemistryRadical polymerizationSolution polymerizationmacromolecular substancesPolymerPolyelectrolyteInorganic Chemistrychemistry.chemical_compoundMonomerchemistryPolymer chemistryMaterials ChemistryOrganic chemistryMacromolecules
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