Search results for "Carbodiimide"

showing 10 items of 21 documents

Effect of different solutions in reversing the damage caused by radiotherapy in dentin structure

2020

Background Previous studies have shown that radiotherapy of the head and neck region can cause direct changes in dental structure. This study evaluated the effect of different solutions on the dentin chemical composition and collagen structure of irradiated dentin. Material and Methods Sixty maxillary canines were distributed in 2 groups (n=30): non-irradiated and irradiated (radiotherapy: X-rays of 6 MV in 30 cycles of 2 Gy to 60 Gy). The teeth were sectioned, sanded, and polished to obtain 3x3x2 mm fragments, which were redistributed in 3 subgroups (n=10) according to the treatment employed: chlorhexidine 2% (CL), chitosan 0.2% (QT), and 0.5 M carbodiimide (EDC). The samples were analyzed…

03 medical and health sciencesHydroxyprolinechemistry.chemical_compound0302 clinical medicinemedicineDentinIrradiationProlineGeneral DentistryCarbodiimideDental structureOral Medicine and PathologyResearchChlorhexidineChlorhexidine030206 dentistry:CIENCIAS MÉDICAS [UNESCO]COMPOSIÇÃO QUÍMICAmedicine.anatomical_structureOtorhinolaryngologychemistryDentinUNESCO::CIENCIAS MÉDICASTukey's range testSurgerymedicine.drugNuclear chemistryMedicina Oral Patología Oral y Cirugia Bucal
researchProduct

[3.3]Ferrocenophanes with guanidine bridging units as multisignalling receptor molecules for selective recognition of anions, cations, and amino acid…

2007

The synthesis, electrochemical, and optical properties of a new [3.3]ferrocenophane framework in which two ferrocene subunits, with similar electronic environments, are linked through two substituted guanidine moieties, are reported. The receptors 4-7 have been prepared in good yields by the reaction of bis(carbodiimide) 3 with primary amines. This architecture is exceptionally "tunable" because a variety of "legs" may be appended to the basic [3.3]ferrocenophane scaffold to give a wide range of signaling units. These receptors show remarkable ion-sensing properties, due to the presence of a redox active unit (ferrocene), and an amphoteric binding site (guanidine). In this nitrogen-rich str…

AnionsModels MolecularMetallocenesInorganic chemistryCrystallography X-RayRedoxCatalysisMetalchemistry.chemical_compoundMolecular recognitionCationsElectrochemistryMoleculeFerrous CompoundsAmino AcidsGuanidineGuanidineCarbodiimideFluorescent Dyeschemistry.chemical_classificationSpectrum AnalysisOrganic ChemistryGeneral ChemistryAmino acidCrystallographyFerrocenechemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Components of an antigen-/T cell receptor-independent pathway of lymphokine production

1991

The general way to induce the synthesis of lymphokines by T cells is the stimulation through the T cell receptor (TcR) complex which results in an increase of intracellular [Ca2+] and in the activation of a tyrosine kinase as well as of protein kinase C. Lymphokine production induced via the TcR is inhibited by the immunosuppressive drug cyclosporin A (CsA). However, an alternative pathway of lymphokine production exists. Several T lymphocyte clones can synthesize interferon-gamma (IFN-gamma), granulocyte-monocyte colony-stimulating factor, and small amounts of interleukin (IL3) when stimulated with syngeneic or allogeneic accessory cells (AC) plus IL2. In contrast to the TcR pathway the al…

Antigens Differentiation T-LymphocyteCD8 AntigensImmunologyT-cell receptorReceptors Antigen T-CellLymphokineAntigen-Presenting CellsCyclosporinsT lymphocyteBiologyCell biologyCarbodiimidesInterferon-gammamedicine.anatomical_structureCell–cell interactionCyclosporin aCD4 AntigensImmunologyAlternative complement pathwaymedicineHumansInterleukin-2Immunology and AllergyAntigen-presenting cellB cellEuropean Journal of Immunology
researchProduct

Involvement of carboxyl groups in chloride transport and reversible DIDS binding to band 3 protein in human erythrocytes

2011

AbstractNoncovalent DIDS binding to Band 3 (AE1) protein in human erythrocyte membranes, modified by non-penetrating, water soluble 1-ethyl-3-(4-azonia-4,4-dimethylpentyl)-carbodiimide iodide (EAC), was studied at 0°C in the presence of 165 mM KCl. Under experimental conditions applied up to (48 ± 5) % of irreversible chloride self-exchange inhibition was observed. The apparent dissociation constant, KD, for “DIDS-Band 3” complex, determined from the chloride transport experiments, was (34 ± 3) nM and (80 ± 12) nM for control and EAC-treated resealed ghosts, respectively. The inhibition constant, Ki, for DIDS was (35 ± 6) nM and (60 ± 8) nM in control and EAC-treated ghosts, respectively. T…

ErythrocytesIodideDissociation constant44'-Diisothiocyanostilbene-22'-Disulfonic AcidTritiumBiochemistryChloridechemistry.chemical_compoundCarbodiimideChloridesAnion Exchange Protein 1 ErythrocytemedicineHumansBinding siteErythrocyte membraneMolecular BiologyBand 3Ion transporterchemistry.chemical_classificationStilbenedisulfonateBinding SitesIon TransportbiologyCooperative bindingCell BiologyDissociation constantBand 3CrystallographyCarbodiimidesKineticsBiochemistrychemistryDIDSbiology.proteinmedicine.drugResearch ArticleProtein BindingCellular & Molecular Biology Letters
researchProduct

Production of specific antibodies and development of a non-isotopic immunoassay for carbamazepine by the carbonyl metallo-immunoassay (CMIA) method.

1995

Abstract As part of our ongoing work to extend the range of applications of the non-isotopic carbonyl metalloimmunoassay (CMIA), previously developed in our laboratory, we describe here the first CMIA study of carbamazepine. The CMIA method uses a metal carbonyl complex as a non-isotopic tracer, and in this case we chose to employ the dicobalt hexacarbonyl moiety (Co2(CO)6) attached to an alkyne. Two organometallic tracers, 3 and 7 , were synthesized, differentiated by the nature and length of the spacer arm of the Co2(CO)6 moiety. Two different coupling methods were subsequently used to synthesize the immunogens 1 and 2, the first one used a carbodiimide, while the second, employed dimethy…

ImmunologyAlkyneCross ReactionsBinding Competitivechemistry.chemical_compoundDimethyl AdipimidateAntibody SpecificityDibenzazepinesSpectroscopy Fourier Transform InfraredmedicineOrganometallic CompoundsImmunology and AllergyMoietyAnimalsCarbodiimidechemistry.chemical_classificationAntiserumImmunoassayChromatographymedicine.diagnostic_testCobaltTiterCarbamazepinechemistryDimethyl AdipimidateDicyclohexylcarbodiimideImmunoassayAnticonvulsantsImmunizationRabbitsQuantitative analysis (chemistry)HaptensJournal of immunological methods
researchProduct

Der 1,3‐Dithian‐2‐ylmethoxycarbonyl‐(Dmoc)‐Rest als Zweistufen‐Schutzgruppe für die Aminofunktion von Aminosäuren und Peptiden

1982

Der 1,3-Dithian-2-ylmethoxycarbonyl-(Dmoc)-Rest (4) als Schutzgruppe fur die Aminofunktion ist gegen Basen und gegen Trifluoressigsaure stabil. Peptidsynthesen mit Dmoc-Aminosauren werden nach dem Mischanhydrid- und nach dem modifizierten Carbodiimid-Verfahren durchgefuhrt. Zur Abspaltung der Dmoc-Schutzgruppe wird diese mit Peressigsaure am Schwefel oxidiert (z. B. zu 13, 14). Die dabei gebildete CH-acide Form kann unter milden basischen Bedingungen von der blockierten Aminofunktion abgelost werden. The 1,3-Dithian-2-ylmethoxycarbonyl (Dmoc) Group as Two-Step Amino Protective Function in Peptide Chemistry The 1,3-dithian-2-ylmethoxycarbonyl (Dmoc) group (4) as amino protective function is …

Inorganic Chemistrychemistry.chemical_classificationchemistry.chemical_compoundChemistryStereochemistryTrifluoroacetic acidPeptide chemistryMoietyPeptideCarbodiimideChemische Berichte
researchProduct

Scaffolds based on hyaluronan crosslinked with a polyaminoacid: Novel candidates for tissue engineering application

2008

New porous scaffolds, with a suitable hydrolytic and enzymatic degradation, useful for tissue engineering applications have been obtained by a carbodiimide mediated reaction between hyaluronan (HA) and a synthetic polymer with a polyaminoacid structure such as α,β-polyaspartylhydrazide (PAHy). Scaffolds with a different molar ratio between PAHy repeating units and HA repeating units have been prepared and characterized from a chemical and physicochemical point of view. Tests of indirect and direct cytotoxicity, cell adhesion, and spreading on these biomaterials have been performed by using murine L929 fibroblasts. The new biomaterials showed a good cell compatibility and ability to allow ce…

Materials scienceCompressive StrengthPolymersBiomedical EngineeringBiomaterialshyaluronanb-polyaspartylhydrazidechemistry.chemical_compoundMiceTissue engineeringMolar ratioCell MovementMaterials TestingCell AdhesionAnimalsHyaluronic AcidCytotoxicityCell adhesionCells CulturedCarbodiimideTissue EngineeringTissue Scaffoldstissue engineering hyaluronic acid chemical crosslinking composite scaffold polyasparthylhydrazideMetals and AlloysCell migrationchemical crosslinkinghyaluronan; a; b-polyaspartylhydrazide; chemical crosslinking; composite scaffolds; tissue engineeringSynthetic polymerPorous scaffoldchemistryChemical engineeringaCeramics and Compositescomposite scaffoldsPeptidesBiomedical engineering
researchProduct

Phosphatidylcholine covalently linked to a methacrylate-based monolith as a biomimetic stationary phase for capillary liquid chromatography

2015

Abstract In this study a strategy to immobilize phospholipids onto a polymer-based stationary phase is described. Methacrylate-based monoliths in capillary format (150 × 0.1 mm) were modified by soybean phosphatidylcholine through 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide coupling to obtain stationary phases suitable to mimic cell surface membranes. The covalent coupling reaction involves the phosphate group in phospholipids; therefore, the described methodology is suitable for all types of phospholipids. Immobilization of soy bean phosphatidylcholine on the monolith was confirmed by attenuated total reflectance Fourier transform infrared spectroscopy and gas chromatography-mass spectro…

Monolithic HPLC columnPolymersPhospholipid010402 general chemistryMethacrylate01 natural sciencesBiochemistryChemistry Techniques AnalyticalAnalytical ChemistryHydrophobic effectchemistry.chemical_compoundBiomimeticsEthyldimethylaminopropyl CarbodiimidePhosphatidylcholineMonolithFourier transform infrared spectroscopyPhospholipidsgeographygeography.geographical_feature_categoryChromatography010401 analytical chemistryOrganic ChemistryWaterGeneral Medicine0104 chemical sciencesMembranechemistryPhosphatidylcholinesMethacrylatesHydrophobic and Hydrophilic InteractionsChromatography LiquidJournal of Chromatography A
researchProduct

Biomolecular conjugation inside synthetic polymer nanopores via glycoprotein-lectin interactions

2011

We demonstrate the supramolecular bioconjugation of concanavalin A (Con A) protein with glycoenzyme horseradish peroxidase (HRP) inside single nanopores, fabricated in heavy ion tracked polymer membranes. Firstly, the HRP-enzyme was covalently immobilized on the inner wall of the pores using carbodiimide coupling chemistry. The immobilized HRP-enzyme molecules bear sugar (mannose) groups available for the binding of Con A protein. Secondly, the bioconjugation of Con A on the pore wall was achieved through its biospecific interactions with the mannose residues of the HRP enzyme. The immobilization of biomolecules inside the nanopore leads to the reduction of the available area for ionic tran…

NanometresSynthetic membraneTransport equationNanoporesInformation processingRectification propertiesCylinders (shapes)Materials TestingConcanavalin AGeneral Materials ScienceFunctional polymersConical nanoporeschemistry.chemical_classificationChemistryBlocking effectElectric rectifiersComputer simulationEnzymesData processingNanoporeEnzyme moleculesFunctional polymersMolecular imprintingPorosityBio-molecularInner wallsMolecular imprintingSupramolecular chemistryNanotechnologyHorseradish peroxidaseIonic transportsNanocapsulesBio-conjugationMoleculeParticle SizeAqueous solutionsGlycoproteinsBiomoleculesBioconjugationBiomoleculeNanostructuresModel simulationChemical engineeringModels ChemicalPolymer membraneConductance stateFISICA APLICADABiospecific interactionSynthetic polymersSugarsSupramolecular chemistryPore wallCarbodiimide-coupling chemistry
researchProduct

Novel cationic copolymers of a polyasparthylhydrazide: synthesis and characterization.

2005

Alpha,beta-poly(asparthylhydrazide) (PAHy), a water soluble synthetic polymer, was functionalized by using EDCI chemistry with 3-(carboxypropyl)trimethyl-ammonium chloride (CPTACl) obtaining carboxypropyltrimethyl ammonium copolymers (PAHy-CPTA). Three PAHy-CPTA copolymers at increasing derivatization degrees (38%, 48%, 58%) were chosen for subsequent investigations. The capability of these copolymers to bind, neutralize, and protect DNA against degradation by DNase II was evalued by gel retardation assay and DNA degradation test at pH 5.5. Zeta potential measurements show that all studied polymers are able to neutralize the anionic charge of DNA at polymer/DNA weight ratio in the range of …

PolymersPharmaceutical ScienceElectrophoretic Mobility Shift AssayElectrolyteChloridechemistry.chemical_compoundElectrolytesCationsPolymer chemistrymedicineCopolymerZeta potentialDerivatizationchemistry.chemical_classificationHEPESEndodeoxyribonucleasesCationic polymerizationpolyplexesGeneral MedicinePolymerDNAQuaternary Ammonium CompoundsCarbodiimideschemistryPeptidesmedicine.drugDrug delivery
researchProduct