Search results for "Derivatization"

showing 10 items of 215 documents

Self-assembling and auto-crosslinkable hyaluronic acid hydrogels with a fibrillar structure

2008

Abstract A hyaluronic acid derivative bearing pendant l -benzoyl-cysteine portions (with a derivatization degree equal to 10 mol.%) was synthesized by linking N,N′-dibenzoyl- l -cystine to the polysaccharide and then reducing its disulfide bridge to thiol groups. The formation of π–π stacking interactions between the benzoyl moieties was studied by fluorescence spectroscopy as a function of polymer concentration and oxidation time. The efficiency of oxidation of thiol groups to disulfide bridges occurring in phosphate buffer pH 7.4, was determined by colorimetric assays. The hydrogel formed by means of oxidative crosslinking has shown the presence of fibrillar aggregates as detected by ligh…

Magnetic Resonance SpectroscopyTime FactorsMaterials scienceCell SurvivalPolymersBiomedical EngineeringCystineStackingBiochemistryFluorescence spectroscopyPhosphatesBiomaterialschemistry.chemical_compoundMaterials TestingSpectroscopy Fourier Transform InfraredPolymer chemistryHyaluronic acidHumansDisulfidesHyaluronic AcidDerivatizationMolecular BiologyCell Proliferationchemistry.chemical_classificationHydrogelsGeneral MedicinePolymerFibroblastsHydrogen-Ion ConcentrationOxygenCross-Linking ReagentschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsMicroscopy Electron ScanningThiolCystineself assembling tissue engineering hyaluronic acid cell entrapmentBiotechnology
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Fluorinated and pegylated polyaspartamide derivatives to increase solubility and efficacy of Flutamide

2012

New fluorinated amphiphilic copolymers based on a biocompatible polyaspartamide have been prepared in order to obtain polymeric micelles useful for delivering anticancer drugs. In particular, α,β-poly(N-2-hydroxyethyl)-d,l-aspartamide (PHEA) has been derivatized with polyethylene glycol (PEG(2000)) and ethylendiamine (EDA). Both these portions form the hydrophilic part of the copolymer, while the hydrophobic moiety is given by 1,2,4-oxadiazoles: 5-pentafluorophenyl-3-perfluoroheptyl-1,2,4-oxadiazole (PPOX) or 3-carboxyethyl-5-pentadecafluoroheptyl-1,2,4-oxadiazole (CPOX). Copolymers named PHEA-PEG(2000)-EDA-PPOX and PHEA-PEG(2000)-EDA-CPOX have been prepared with various degrees of derivati…

MaleAntineoplastic Agents HormonalPolymersSize-exclusion chromatographyPharmaceutical SciencePolyethylene glycolAdenocarcinomaPolyethylene Glycolschemistry.chemical_compoundDrug Delivery SystemsCell Line TumorPolymer chemistryCopolymerHumansSolubilityDerivatizationMicellesCell Proliferationchemistry.chemical_classificationDrug CarriersOxadiazolesProstatic NeoplasmsDihydrotestosteroneSettore CHIM/06 - Chimica OrganicaPolymerEthylenediaminesFlutamideCancer targeting cell model colloidal particles drug delivery polymerSolubilitychemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryChromatography GelMicroscopy Electron ScanningPyrenePeptidesHydrophobic and Hydrophilic InteractionsJournal of Drug Targeting
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Synthesis and evaluation of thermo-rheological behaviour and ionotropic crosslinking of new gellan gum-alkyl derivatives.

2018

Abstract This paper reports the synthesis and the physicochemical characterization of two series of gellan gum (GG) derivatives functionalized with alkyl chains with different number of carbon, from 8 to 18. In particular, low molecular weight gellan gum samples with 52.6 or 96.7 kDa, respectively, were functionalized with octylamine (C8), dodecylamine (C12) and octadecylamine (C18) by using bis(4-nitrophenyl) carbonate (4-NPBC) as a coupling agent. Thermo-rheological and ionotropic crosslinking properties of these gellan gum-alkyl derivatives were evaluated and related to the degree of derivatization in alkyl chains. Results suggested as length and degree of derivatization differently infl…

Materials Chemistry2506 Metals and AlloysPolymers and Plastics02 engineering and technologymacromolecular substances010402 general chemistry01 natural sciencesAlkylaminesGellan gumAlkylaminechemistry.chemical_compoundRheologyPolymer chemistryMaterials ChemistryDerivatizationAlkylchemistry.chemical_classificationPolymers and PlasticOrganic ChemistryHydrogels021001 nanoscience & nanotechnologyGellan gum0104 chemical sciencesHydrogelchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogels0210 nano-technologyRheologyIonotropic effectCarbohydrate polymers
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NANOPARTICLES BASED ON NOVEL AMPHIPHILIC POLYASPARTAMIDE COPOLYMERS

2010

In this article, the synthesis of two amphiphilic polyaspartamide copolymers, useful to obtain polymeric nanoparticles without using surfactants or stabilizing agents, is described. These copolymers were obtained starting from α,β-poly-(N-2-hydroxyethyl)-dl-aspartamide (PHEA) by following a novel synthetic strategy. In particular, PHEA and its pegylated derivative (PHEA-PEG2000) were functionalized with poly(lactic acid) (PLA) through 1,1′-carbonyldiimidazole (CDI) activation to obtain PHEA–PLA and PHEA-PEG2000–PLA graft copolymers, respectively. These copolymers were properly purified and characterized by 1H-NMR, FT-IR, and Size Exclusion Chromatography (SEC) analyses, which confirmed that…

Materials scienceALPHABETA-poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) poly(lactic acid) (PLA) poly(ethylene glycol) (PEG) graft copolymers nanoparticlesSize-exclusion chromatographytechnology industry and agricultureNanoparticleBioengineeringGeneral Chemistrymacromolecular substancesCondensed Matter PhysicsAtomic and Molecular Physics and Opticschemistry.chemical_compoundX-ray photoelectron spectroscopychemistrystomatognathic systemSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoModeling and SimulationAmphiphilePolymer chemistryPEG ratioCopolymerZeta potentialGeneral Materials ScienceDerivatization
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Construction and evaluation of sponge scaffolds from hyaluronic acid derivatives for potential cartilage regeneration

2020

A two or one pot synthesis has been used for the reaction of hyaluronic acid (HA) with octadecylamine (C-18) and hydrazine (Hy). In both cases, the chemical derivatization involved primary hydroxyl groups of hyaluronic acid and not its carboxyl groups, whose presence is important for receptor interaction. In this way, Hy-HA-C-18 derivatives have been obtained with appropriate hydrophobic and hydrophilic character. Their ability to form homogeneous physical hydrogels has been evaluated as well as the possibility to obtain porous sponges through salt leaching technology. Sponges showing the highest porosity, potentially compatible with cell entrapment, have been characterized with regard to t…

Materials scienceBiomedical EngineeringSettore MED/08 - Anatomia PatologicaGlycosaminoglycanchemistry.chemical_compoundPhysiological conditionHyaluronidaseChemical derivatizationHyaluronic acidmedicineOrganic chemistryGeneral Materials ScienceHydrophobic and hydrophilicDerivatizationbiologyCartilageBovine chondrocyteGeneral ChemistryGeneral Medicinebiology.organism_classificationHyaluronic acid derivativeReceptor interactionSpongemedicine.anatomical_structurechemistryCartilage regenerationSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsBiological propertieSwellingmedicine.symptommedicine.drugNuclear chemistryJournal of Materials Chemistry B
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Effect of alkyl derivatization of gellan gum during the fabrication of electrospun membranes

2021

Electrospun nanofibers based on polysaccharides represent a consolidated approach in Tissue Engineering and Regenerative Medicine (TERM) and nanomedicine as a drug delivery system (DDS). In this work, two chemical derivatives of a low molecular weight gellan gum (96.7 kDa) with aliphatic pendant tails were processed by electrospinning technique into non-woven nanofibrous mats. In order to generate spinnable blends, it was necessary to associate poly vinyl alcohol (PVA). The relationships between the physicochemical properties and the processability via electrospinning technique of gellan gum alkyl derivatives (GG-C8 and GG-C12 having a degree of alkyl chain derivatization of 17 mol % and 1…

Materials sciencePolymers and PlasticsMaterials Science (miscellaneous)02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing Engineeringchemistry.chemical_compoundTissue engineeringelectrospinning; gellan gum; nanofibers; PVAnanofibersChemical Engineering (miscellaneous)DerivatizationAlkylchemistry.chemical_classificationElectrospinning021001 nanoscience & nanotechnologyGellan gumElectrospinning0104 chemical scienceschemistryChemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNanofiberDrug deliveryPVANanomedicine0210 nano-technologygellan gum
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Hepatocyte-targeted fluorescent nanoparticles based on a polyaspartamide for potential theranostic applications

2015

Abstract Here, the synthesis of a galactosylated amphiphilic copolymer bearing rhodamine (RhB) moieties and its use for the preparation of polymeric fluorescent nanoparticles for potential applications in therapy and diagnosis are described. To do this, firstly, a fluorescent derivative of α,β-poly( N -2-hydroxyethyl)- d , l -aspartamide (PHEA) was synthesized by chemical reaction with RhB, and with polylactic acid (PLA), to obtain PHEA-RhB-PLA. Then, the derivatization of PHEA-RhB-PLA with GAL-PEG-NH 2 allows obtaining PHEA-RhB-PLA-PEG-GAL copolymer, with derivatization degrees in -PLA and -PEG-GAL equal to 1.9 mol% and 4.5 mol%, respectively. Starting from this copolymer, liver-targeted f…

Materials sciencePolymers and PlasticsOrganic Chemistrytechnology industry and agricultureNanoparticlemacromolecular substancesCombinatorial chemistryFluorescenceRhodaminechemistry.chemical_compoundPolylactic acidchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPolymer chemistryMaterials ChemistryZeta potentialCopolymerAsialoglycoprotein receptorActive targeting alphabeta-Poly-(N-2-hydroxyethyl)-DL-aspartamide (PHEA) Fluorescence imaging Graft copolymers NanoparticlesDerivatization
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LC-MS/MS characterisation and determination of dansyl chloride derivatised glyphosate, aminomethylphosphonic acid (AMPA), and glufosinate in foods of…

2021

Abstract Glyphosate and other polar and acidic pesticides have been particularly studied due to the concerns over widespread and intensive use. The chemical properties of these compounds necessitate use of customised methods, such as derivatisation or ion exchange chromatography. These approaches present a compatibility problem with ESI-MS due to presence of salts and non-volatile compounds. For that reason, a simple procedure has been developed for the extraction, pre-column derivatisation with dansyl chloride (5-(dimethylamino)naphthalene-1-sulfonyl chloride), and mass spectrometric detection of glyphosate, AMPA, and glufosinate after the separation on a C18 stationary phase. The dansyl d…

MeatClinical BiochemistryIon chromatographyOrganophosphonatesIon suppression in liquid chromatography–mass spectrometry030226 pharmacology & pharmacy01 natural sciencesBiochemistryAnalytical ChemistryMatrix (chemical analysis)03 medical and health scienceschemistry.chemical_compound0302 clinical medicineTandem Mass SpectrometryAnimalsAminomethylphosphonic acidDerivatizationDansyl CompoundsChromatographyAminobutyrates010401 analytical chemistryDansyl chlorideExtraction (chemistry)Pesticide ResiduesCell BiologyGeneral MedicineHoney0104 chemical scienceschemistryReagentCattleCucumis sativusFood AnalysisChromatography LiquidJournal of chromatography. B, Analytical technologies in the biomedical and life sciences
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Green Analytical Chemistry Past, Present and Perspectives

2019

The book explains the principles and fundamentals of Green Analytical Chemistry (GAC) and highlights the current developments and future potential of the analytical green chemistry-oriented applications of various solutions. The book consists of sixteen chapters, including the history and milestones of GAC; issues related to teaching of green analytical chemistry and greening the university laboratories; evaluation of impact of analytical activities on the environmental and human health, direct techniques of detection, identification and determination of trace constituents; new achievements in the field of extraction of trace analytes from samples characterized by complex composition of the…

MicroextractionPassive techniquesPollution remote monitoringGreen chromatographyDerivatization processGreen solventsGreen analytical techniquesGreen sorption materialsGreen Analytical ChemistryDirect techniques
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Synthesis of site-heterologous haptens for high-affinity anti-pyraclostrobin antibody generation.

2011

The design and synthesis of functional chemical derivatives of small organic molecules is usually a key step for the intricate production of a variety of bioconjugates. In this respect, the derivatization site at which the spacer arm is introduced in immunizing conjugates constitutes a highly critical parameter for the generation of high-affinity and selective antibodies. However, due to the usual complexity of the required synthetic procedures, the appropriate comparison of alternative tethering positions has often been neglected. In the present study, meticulous strategies were followed to prepare synthetic derivatives of pyraclostrobin with the same linkers located at diverse rationally-…

Models MolecularMolecular modelStereochemistryHeterologousBiochemistryAntibodieschemistry.chemical_compoundAntibody generationMoleculePhysical and Theoretical ChemistryImmunoassaysDerivatizationBioconjugationMolecular StructureOrganic ChemistryStrobilurinsCombinatorial chemistryAffinitieschemistryComputer assisted molecular modelingPyrazolesCarbamatesHaptenHaptensConjugateOrganicbiomolecular chemistry
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