Search results for "SOLID-PHASE"

showing 10 items of 178 documents

DNA Block Copolymer Micelles – A Combinatorial Tool for Cancer Nanotechnology

2008

Selective drug targeting of a specific organ or tissue is a challenging task. This holds especially true for chemotherapeutic cancer treatment because most of the available anticancer agents cannot distinguish between cancerous and healthy cells, leading to systemic toxicity and undesirable side effects. One effective approach to address this problem is the application of polymeric nanoparticles equipped with targeting units for tumor-specific delivery. For instance dendrimers, highly branched macromolecules, can be equipped with targeting units as well as with anticancer drugs because of their large number of surface functionalities. Amphiphilic block copolymers, which self-assemble in dil…

Materials scienceMechanical EngineeringCombinatorial chemistryMicelleSolid-phase synthesisTargeted drug deliveryMechanics of MaterialsColloidal goldDendrimerAmphiphileDrug deliveryComputingMethodologies_DOCUMENTANDTEXTPROCESSINGCopolymerGeneral Materials ScienceGeneralLiterature_REFERENCE(e.g.dictionariesencyclopediasglossaries)Advanced Materials
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Microextraction with phases containing nanoparticles.

2015

In this article, the state of the art of microextraction techniques that involve nanoparticles or nanomaterials (NPs) is reviewed, with special emphasis on the applications described in the biomedical field. The uses and advantages of the different types of NPs such as carbon nanotubes (either single- and multi-walled) and other carbon-based materials, metallic NPs, including gold, silver and magnetic NPs, and silica NPs are summarized. The main strategies used to modify the selectivity, extractive capacity and/or the stability of NPs through a chemical reaction are also reviewed. The potential advantages of NPs in different forms of off-line and on-line microextraction are discussed, and …

Materials scienceNanotubes CarbonClinical BiochemistryNanoparticlechemistry.chemical_elementNanotechnologyGeneral MedicineCarbon nanotubeSolid-phase microextractionAnalytical Chemistrylaw.inventionNanomaterialsMedical Laboratory TechnologychemistrylawMagnetsHumansNanoparticlesGeneral Pharmacology Toxicology and PharmaceuticsCarbonSolid Phase MicroextractionBioanalysis
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Redox-responsive organometallic foldamers from ferrocene amino acid: Solid-phase synthesis, secondary structure and mixed-valence properties

2011

Oligoferrocenes Fmoc-Fca(n)-OMe (n=3-5) are assembled in a stepwise precise manner from Fmoc-protected ferrocene amino acid Fmoc-Fca-OH (H-Fca-OH = 1-amino-1'-ferrocene carboxylic acid; Fmoc = 9-fluorenylmethyloxycarbonyl) via amide bonds on solid supports by sequential Fmoc deprotection, acid activation and coupling steps. The resulting well-defined oligomers form ordered zigzag structures in THF solution with characteristic hydrogen bonding patterns. Electrochemical experiments reveal sequential oxidations of the individual ferrocene units in these peptides giving mixed-valent cations. Optical intervalence electron transfer is detected by intervalence transitions in the near-IR.

Models MolecularMetallocenesStereochemistryCarboxylic acidProtein Structure SecondaryInorganic Chemistrychemistry.chemical_compoundElectron transferSolid-phase synthesisPolymer chemistryOrganometallic CompoundsFerrous CompoundsAmino AcidsProtein secondary structurechemistry.chemical_classificationFluorenesValence (chemistry)Hydrogen bondSpectrum AnalysisDipeptidesAmino acidSolutionschemistryFerrocenePeptidomimeticsOxidation-ReductionDalton Transactions
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Saccharide-induced peptide conformation in glycopeptides of the recognition region of LI-cadherin.

2006

Models MolecularStereochemistryChemistryCadherinMolecular Sequence DataGlycopeptidesGeneral ChemistryCadherinsCrystallography X-RayCatalysisGlycopeptidePeptide ConformationProtein Structure TertiaryLI-CADHERINSolid-phase synthesisBiochemistryCarbohydrate ConformationCarbohydrate conformationAmino Acid SequencePeptide sequenceNuclear Magnetic Resonance BiomolecularAngewandte Chemie (International ed. in English)
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Bioinspired manganese(II) complexes with a clickable ligand for immobilisation on a solid support.

2014

International audience; Clickable ligands like N,N′-bis((pyridin-2-yl)methyl)prop-2-yn-1-amine (L1) and N-((1-methyl-1H-imidazol-2-yl)methyl)-N-(pyridin-2-ylmethyl)prop-2-yn-1-amine (L2) have been used to synthesise a series of manganese(II) complexes for grafting onto appropriate solid supports. These ligands mimic the 2-His-1-carboxylate facial chelation present in the active site of the manganese-dependent dioxygenase (MndD), while the alkyne side function allows grafting of the ligand onto an azido-functionalised support using “click chemistry” methodologies. Such synthetic analogues of the MndD crystallise in the solid state as double halide or pseudohalide-bridged dinuclear manganese(…

Models MolecularStereochemistryMolecular ConformationAlkynechemistry.chemical_elementManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryCrystallography X-RayLigands01 natural scienceslaw.inventionDioxygenasesInorganic ChemistrylawCoordination ComplexesCatalytic DomainPolymer chemistryChelationElectron paramagnetic resonanceSolid-Phase Synthesis Techniqueschemistry.chemical_classificationManganesebiology010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryElectron Spin Resonance SpectroscopyActive site[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.MATE]Chemical Sciences/Material chemistrySilicon Dioxide0104 chemical scienceschemistrySuperexchangebiology.proteinClick chemistryClick ChemistryDalton transactions (Cambridge, England : 2003)
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Synthesis and Structural Model of an α(2,6)-Sialyl-T Glycosylated MUC1 Eicosapeptide under Physiological Conditions

2006

To study the effect of O-glycosylation on the conformational propensities of a peptide backbone, a 20-residue peptide (GSTAPPAHGVTSAPDTRPAP) representing the full length tandem repeat sequence of the human mucin MUC1 and its analogue glycosylated with the (2,6)-sialyl-T antigen on Thr11, were prepared and investigated by NMR and molecular modeling. The peptides contain both the GVTSAP sequence, which is an effective substrate for GalNAc transferases, and the PDTRP fragment, a known epitope recognized by several anti-MUC1 monoclonal antibodies. It has been shown that glycosylation of threonine in the GVTSAP sequence is a prerequisite for subsequent glycosylation of the serine at GVTSAP. Furt…

Models Molecularchemistry.chemical_classificationMagnetic Resonance SpectroscopyGlycosylationMolecular modelChemistryStereochemistryMucin-1Organic ChemistryGlycopeptidesTemperaturePeptideGeneral ChemistryCatalysisEpitopecarbohydrates (lipids)Turn (biochemistry)chemistry.chemical_compoundSolid-phase synthesisBiochemistryBiomimeticsThermodynamicsIndicators and ReagentsProtein secondary structureMUC1Chemistry - A European Journal
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Stereoselective solid-phase synthesis of chiral piperidine derivatives by using an immobilized galactose auxiliary.

2003

Molecular StructurePolymersGalactoseGalactosamineStereoisomerismGeneral ChemistryCatalysischemistry.chemical_compoundSolid-phase synthesischemistryPiperidinesGalactoseOrganic chemistryStereoselectivityPiperidineAngewandte Chemie (International ed. in English)
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Carbohydrate Scaffolds for Combinatorial Syntheses That Allow Selective Deprotection of All Four Positions Independent of the Sequence

2004

Molecular StructureStereochemistryChemistryCarbohydratesStereoisomerismGeneral ChemistryCarbohydrateCombinatorial chemistryMass SpectrometryCatalysisSolid-phase synthesisThioglycosidesDrug DesignCombinatorial Chemistry TechniquesGlycosidesChromatography High Pressure LiquidSequence (medicine)Angewandte Chemie International Edition
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Determination of ketosteroid hormones in meat by liquid chromatography tandem mass spectrometry and derivatization chemistry.

2015

A method for the determination and quantification of ketosteroid hormones in meat by mass spectrometry, based on the derivatization of the carbonyl moiety of steroids by O-methylhydroxylamine, is presented. The quantitative assay is performed by means of multiple-reaction-monitoring (MRM) scan mode and using the corresponding labelled species, obtained by reaction with d 3-methoxylamine, as internal standard. The accuracy of the method was established by evaluating artificially spiked samples, obtaining values in the range 90-110%. Recovery tests were performed on blank matrix samples spiked with non-natural steroids including trenbolone and melengestrol acetate. The latter experiment revea…

Multiple reaction monitoringChromatographyMeatMass spectrometrySelected reaction monitoringKetosteroidMass spectrometrySolid-phase microextractionKetosteroidsBiochemistryAnalytical ChemistryMatrix (chemical analysis)chemistry.chemical_compoundTrenbolonechemistryLiquid chromatography–mass spectrometryTandem Mass SpectrometryKetosteroidMethoxylamineUHPLCmedicineDerivatizationSolid Phase Microextractionmedicine.drugAnalytical and bioanalytical chemistry
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Combining poly(dimethyldiphenylsiloxane) and nitrile phases for improving the separation and quantitation of benzalkonium chloride homologues: In-tub…

2013

The retention and separation of four homologues of benzalkonium chloride (alkyl (C12, C14, C16, C18) dimethylbenzylammonium chloride) have been studied in poly(dimethyldiphenylsiloxane) (TRB) and nitrile capillary phases, respectively. Under the optimized conditions (50% acetonitrile in processed samples, 35% of diphenyl content of the TRB, capillary length 43 cm and water:methanol 60:40 as replacing solvent), the extraction efficiency was similar for all the homologues with satisfactory reproducibility and independently of the amount and proportion of homologues. Industrial samples with high viscosity or with complex composition and washes waters have been analyzed without previous treatme…

NitrileSolid-phase microextractionMass spectrometryBiochemistryChlorideMass SpectrometryAnalytical ChemistryBenzalkonium chloridechemistry.chemical_compoundLimit of DetectionNitrilesmedicineDimethylpolysiloxanesAcetonitrileSolid Phase MicroextractionChromatographyChemistryOrganic ChemistryExtraction (chemistry)Reproducibility of ResultsGeneral MedicineSolventLinear Modelslipids (amino acids peptides and proteins)Benzalkonium Compoundsmedicine.drugChromatography LiquidJournal of chromatography. A
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