Search results for " modifica"

showing 10 items of 817 documents

Sul Miglioramento della Processabilità del Nanocomposito a base di Polistirene Sindiotattico e Argille Modificate

2004

Sul Miglioramento della Processabilità del Nanocomposito a base di Polistirene Sindiotattico e Argille Modificate

Polistirene SindiotatticoArgille ModificateProcessabilitàNanocomposito
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Influence of the xyloadenosine analogue of 2?,5?-oligoriboadenylate on poly(A)-specific, 2?,5?-oligoriboadenylate degrading 2?,3?-exoribonuclease and…

1984

The homogeneous poly(A)-specific 2′,3′-exoribonuclease from calf thymus gland, which cleaves both 3′,5′-and 2′,5′-linked oligoriboadenylates, does not degrade (xyloA2'p)2 xyloA, the xylofuranosyladenosine analogue of the 2-5A core. This oligonucleotide, which is supposed to enter intact cells rapidly, was found to possess an increased stability and an enhanced antiherpesvirus activity compared to the natural (A2'p)2A (Eppstein, D. A., Barnett, J. W., Marsh, Y. V., Gosselin, G. and Imbach, J.-L. (1983) Nature 302, 723–724). The poly(A) anabolic enzyme, poly(A) polymerase (Mn2+-dependent), from the same source, which is initiated by (A3'p)2A and its higher oligomers, does not accept 2–5A core…

PolyadenylationOligonucleotidesIn Vitro TechniquesOligomerchemistry.chemical_compoundExoribonucleaseEndoribonucleasesGeneticsAnimalsRNA MessengerMolecular BiologyPolymerasechemistry.chemical_classificationOligoribonucleotidesbiologyAdenine NucleotidesOligonucleotidePolynucleotide AdenylyltransferaseGeneral MedicineMolecular biologyPost-transcriptional modificationEnzymeRibonucleoproteinsBiochemistrychemistryExoribonucleasesbiology.proteinCattlePrimer (molecular biology)Poly AMolecular Biology Reports
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SURFACE MODIFICATION OF EAA WITH FUNCTIONALIZED SILICA NANOPARTICLES

2009

Polymer surface modificationSettore ING-IND/22 - Scienza E Tecnologia Dei Materialisilica nanoparticlegrafting tomelt processinggrafting fromHybrid material
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Carboranyl Substituted Siloxanes and Octasilsesquioxanes: Synthesis, Characterization, and Reactivity

2008

Carboranyl-containing disiloxane, cyclic-siloxane and cage-like silsesquioxane have been prepared in high yields. Two routes are compared for their preparation, a classical hydrolytic process based on hydrolysis and condensation of the freshly prepared carboranylalkylchlorosilane and ethoxysilane precursors and a nonhydrolytic route based on the specific reactivity of chorosilane toward DMSO. Based on the typical reactivity of the carboranyl group toward nucleophiles, dianionic disiloxanes and octaanionic silsesquioxanes were obtained without modification of the siloxane bond. Products are fully characterized by FTIR, NMR and MALDI-TOF methods.

Polymers and Plastics010405 organic chemistryOrganic ChemistryChemical modification[CHIM.MATE]Chemical Sciences/Material chemistryDisiloxane010402 general chemistry01 natural sciencesSilsesquioxane0104 chemical sciencesInorganic Chemistrychemistry.chemical_compound[CHIM.POLY]Chemical Sciences/PolymersNucleophilechemistrySiloxanePolymer chemistryMaterials ChemistryCarboraneOrganic chemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryReactivity (chemistry)ComputingMilieux_MISCELLANEOUSMacromolecules
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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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Modification of carboxyl groups of poly(ethylene-co-acrylic acid) via facile wet chemistry method: A kinetic study

2010

Abstract In this work, we present the results of a kinetic study of the surface modification of the carboxyl group of poly(ethylene-co-acrylic acid) into acyl chloride. Reaction temperature and time, concentration of the reactants, kind of agitation have been changed in order to understand their effect on the conversion. A study on the penetration of the reaction inside the sample bulk was also performed. The results indicate that, when short reaction times are adopted, the reaction limits to the outer layers of the samples and, in this case, on increasing the temperature, the concentration of the reactants and the stirring allows having a faster kinetic. At longer reaction times, the react…

Polymers and PlasticsGeneral Chemical EngineeringChemical modificationGeneral ChemistryPenetration (firestop)BiochemistryContact anglechemistry.chemical_compoundPoly(ethylene-co-acrylic acid)Surface modificationSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryAcyl chlorideChemical engineeringPolymer chemistryMaterials ChemistryEnvironmental ChemistrySurface modificationFourier transform infrared spectroscopyFunctionalizationWet chemistryAcrylic acid
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An assembly of organic-inorganic composites using halloysite clay nanotubes

2018

Halloysite is natural tubular clay suitable as a component of biocompatible nanosystems with specific functionalities. The selective modification of halloysite inner/outer surfaces can be achieved by exploiting supramolecular and covalent interactions resulting in controlled colloidal stability adjusted to the solvent polarity. The functionalized halloysite nanotubes can be employed as reinforcing filler for polymers as well as carriers for the sustained release of active molecules, such as antioxidants, flame-retardants, corrosion inhibitors, biocides and drugs. The tubular morphology makes halloysite a perspective template for core-shell metal supports for mesoporous catalysts. The cataly…

Polymers and PlasticsHalloysite nanotube02 engineering and technologyReview01 natural sciencesunclassified drug adsorptionFlame retardantcovalent bondColloid and Surface ChemistryhalloysiteControlled drug deliverychemistry.chemical_classificationemulsionquantum dotSurfaces and InterfacesPolymerSelf assembly021001 nanoscience & nanotechnologynanorodPickering emulsionCorrosion inhibitoroil spillSolventSelective modification Kaolinite chemicals and drugNanorodBiocompatibility0210 nano-technologyOil water interfaceYarn Covalent interactionNanotubeMaterials scienceSupramolecular chemistrysustained drug releasecatalysiengineering.material010402 general chemistryHalloysitebioremediationPhysical and Theoretical ChemistryhydrophobicityMesoporous catalystpetroleummetal nanoparticlePhase interfacemetal bindingReinforcing fillerPickering emulsion0104 chemical sciencesOrganic-inorganic compositeNanotubeFilled polymerchemistryChemical engineeringengineeringSelf-assemblyCatalystMesoporous material
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Synthesis and Characterization of Poly(glyceryl glycerol) Block Copolymers

2008

Polymers and PlasticsOrganic ChemistryChemical modificationRing-opening polymerizationCharacterization (materials science)Inorganic ChemistryHydrolysischemistry.chemical_compoundAnionic addition polymerizationchemistryPolymer chemistryMaterials ChemistryCopolymerGlycerolOrganic chemistryMacromolecules
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"A versatile post-polymerization modification method for polyglutamic acid: synthesis of orthogonal reactive polyglutamates and their use in ""click …

2013

In this article we describe a versatile methodology for the synthesis of polyglutamic acid (PGA) derivatives bearing orthogonal reactive sites. The reactive groups enable selective conjugation chemistry by copper catalyzed azide-alkyne coupling (CuAAC). PGA was derived in aqueous media as well as in organic media using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl morpholinium chloride (DMTTM) salts. The spectra of attached chemical moieties ranges from simple PEGylation with 2,5,8,11,14,17,20-heptaoxadocosan-22-amine (mEG(6)NH2) to the incorporation of propargylamine, 11-azido-3,6,9-trioxaundecan-1-amine (NH2-EG(2)N-3), and 20-azido-3,6,9,12,15,18-hexaoxaicosan-1-amine (NH2-EG(6)N-3). Here…

Polymers and PlasticsOrganic ChemistryPolyglutamic acidBioengineering02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCombinatorial chemistryOrganic mediaChloride0104 chemical scienceschemistry.chemical_compoundchemistryPEGylationClick chemistrymedicineOrganic chemistrySurface modification0210 nano-technologyPost polymerizationmedicine.drug
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HPMC-salicylate conjugates as macromolecular prodrugs: Design, characterization, and nano-rods formation

2009

The design, characterization, and nano-rods formation of hydroxypropylmethylcellulose (HPMC)-salicylate conjugates as macromolecular prodrugs, was described. HPMC, obtained from Zhejiang Zhongbao Imp and Exp Corp, was dried under vacuum at 110°C for 8 hr. Nanoparticles were prepared using dialysis process in which 170 mg of HPMC-salicylate sample was dissolved in 5 mL of purified DMSO and was dialyzed against distilled water for 4 days. HPMC-salicylic acid conjugates reveal the absence of sulfur in all of the samples showing that there is no introduction to tosylate groups either covalently bounded or as an impurity.

Polymers and PlasticsOrganic Chemistrytechnology industry and agricultureChemical modificationProdrugbody regionschemistry.chemical_compoundchemistryDistilled waterCovalent bondMaterials ChemistryOrganic chemistrySelf-assemblyDrug carrierSalicylic acidNuclear chemistryConjugateJournal of Polymer Science Part A: Polymer Chemistry
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