Search results for "lipids"

showing 10 items of 2228 documents

Tuning of biodegradation rate of PLLA scaffolds via blending with PLA

2009

Blends of Poly-L-Lactic Acid (PLLA) with Poly-Lactic Acid (PLA) in different proportions (95/5, 90/10, 80/20, 70/30 and 60/40) were utilized in order to realize biodegradable and biocompatible scaffolds for soft tissue engineering applications. The scaffolds were produced via thermally induced phase separation (TIPS) starting from ternary systems where dioxane was the solvent and water the non-solvent. Morphology was evaluated by Scanning Electron Microscopy (average pore size and interconnection). Foams’ apparent density was also evaluated (porosity ranges from 87% to 92%). Moreover an in vitro biodegradation test of scaffolds was set-up in order to verify the rate of degradation of the va…

chemistry.chemical_classificationMorphology (linguistics)Materials scienceScanning electron microscopePolymerBiodegradationSolventTissue engineeringchemistryDegradation (geology)lipids (amino acids peptides and proteins)General Materials ScienceTissue engineering Scaffold PLA PLLA Blends BiodegradationComposite materialPorosityInternational Journal of Material Forming
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Alkylation of lithium dienediolates of butenoic acids. Regioselectivity effects of structure and leaving group of the alkylating agent

1998

Abstract Regioselectivity of alkylation of but-2-enoic acids 1 and 2 by alkyl halides strongly depends on the reactivity of the electrophile. High α selectivity results for saturated alkyl halides, whereas poor α-selectivity is obtained for highly reactive allyl and benzyl halides. For reactive alkylating halides selectivity is partly governed by the ion pairing aggregates of the dienediolates. Lithium bromide and the carboxylate generated in the ongoing reaction cause opposite effects on regioselectivity.

chemistry.chemical_classificationOrganic ChemistryLeaving groupRegioselectivityAlkylationBiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryDrug DiscoveryElectrophileOrganic chemistrylipids (amino acids peptides and proteins)Reactivity (chemistry)CarboxylateSelectivityAlkylTetrahedron
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Synthetic Tumor-Associated Glycopeptide Antigens from the Tandem Repeat Sequence of the Epithelial Mucin MUC4

2004

In cancer research, the development of vaccines against tumor-associated antigens is of particular interest. Epithelial cells express mucin type glycoproteins, which are extensively O-glycosylated. In case of cancer, the expression of these mucins is increased, and their carbohydrate side chains show an aberrant glycosylation pattern. A set of single and double glycosylated hexadecapeptides representing the tandem repeat sequence of the epithelial mucin MUC4 carrying different tumor-associated carbohydrate antigens was prepared by sequential solid-phase glycopeptide synthesis. The crucial glycosyl amino acid building blocks containing the T N , T, sialyl-T N and (2,6)-sialyl-T antigens were…

chemistry.chemical_classificationOrganic ChemistryMucinGeneral MedicineMolecular biologyCatalysisGlycopeptideAmino acidcarbohydrates (lipids)chemistry.chemical_compoundSolid-phase synthesisAntigenchemistryBiochemistryGalactosamineGlycosylThreonineGlycoproteinSynthesis
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Synthesis and Characterization of theO-Alkylation Products of Resorcinarene

2013

O-Substitution reactions of tetramethoxyresorcinarene with alkyl halides produced a variety of partially O-alkylated resorcinarene derivatives with terminal alkyne functionality. The degree of alkylation was affected by the reactivity of the alkylating halide used. NMR spectroscopy proved to be an ideal tool for analyzing the complex reaction mixtures and the isolated products based on the symmetry and degree of alkylation of the resorcinarene derivatives. Single-crystal X-ray diffraction studies furthermore showed diversity in the self-assembly of the various O-alkylation products that was greatly affected by the degree of alkylation, as well as the nature of the alkyne moiety.

chemistry.chemical_classificationOrganic ChemistrySupramolecular chemistryAlkyneNuclear magnetic resonance spectroscopyAlkylationResorcinarenechemistryMoietyOrganic chemistrylipids (amino acids peptides and proteins)Reactivity (chemistry)Physical and Theoretical ChemistryAlkylEuropean Journal of Organic Chemistry
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Calculation of the Phase Behavior of Lipids

1998

The self-assembly of monoacyl lipids in solution is studied employing a model in which the lipid's hydrocarbon tail is described within the Rotational Isomeric State framework and is attached to a simple hydrophilic head. Mean-field theory is employed, and the necessary partition function of a single lipid is obtained via a partial enumeration over a large sample of molecular conformations. The influence of the lipid architecture on the transition between the lamellar and inverted-hexagonal phases is calculated, and qualitative agreement with experiment is found.

chemistry.chemical_classificationPartition function (quantum field theory)Quantitative Biology::BiomoleculesStatistical Mechanics (cond-mat.stat-mech)010304 chemical physicsChemistryFOS: Physical sciencesThermodynamics02 engineering and technology021001 nanoscience & nanotechnology01 natural sciencesMolecular conformationLarge sampleQuantitative Biology::Subcellular ProcessesCondensed Matter::Soft Condensed MatterHydrocarbonPhase (matter)0103 physical sciencesLamellar structurelipids (amino acids peptides and proteins)Lipid bilayer phase behavior0210 nano-technologyCondensed Matter - Statistical Mechanics
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Does catalase play a role in Adriamycin induced cardiotoxicity?

1980

Summary Adriamycin causes an increase of lipid peroxidation in mouse cardiac homogenates that is dependent on the concentration of the antiblastic. The same phenomenon is not observed in the hearts of mice treated with an elevated dose of Adriamycin in which, conversely, an increase of the antioxidizing enzyme catalase was noticed. The significance of these findings is discussed with relationship to the hypothesis of an enhanced free radicals formation at the basis of Adriamycin induced cardiotoxicity.

chemistry.chemical_classificationPharmacologyCardiotoxicityLipid PeroxidesbiologyFree RadicalsHeart DiseasesMyocardiumPharmacologyNADCatalaseMalonatescarbohydrates (lipids)Lipid peroxidationchemistry.chemical_compoundMiceEnzymechemistryCatalaseDoxorubicinMalondialdehydepolycyclic compoundsbiology.proteinAnimalsFemalePharmacological Research Communications
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Polyunsaturated fatty acids in the modulation of T-cell signalling

2009

n-3 polyunsaturated fatty acids (PUFA) have been shown to modulate immune responses. These agents, being considered as adjuvant immunosuppressants, have been used in the treatment of various inflammatory and autoimmune diseases. However, the molecular mechanisms of action of n-3 PUFA-induced immunosuppressive effects are not well-understood. Since exogenous n-3 PUFA, under in vitro and in vivo conditions, are efficiently incorporated into T-cell plasma membranes, a number of recent studies have demonstrated that these agents may modulate T-cell signalling. In this review, the interactions of n-3 PUFA with the second messenger cascade initiated during early and late events of T-cell activati…

chemistry.chemical_classificationPhospholipase DT-LymphocytesClinical BiochemistryCell BiologyBiologyLymphocyte ActivationModels BiologicalDiglyceridesMembrane MicrodomainsBiochemistrychemistryDocosahexaenoic acidFatty Acids Omega-3Second messenger systemFatty Acids UnsaturatedAnimalsHumanslipids (amino acids peptides and proteins)Signal transductionProtein kinase CSignal TransductionCalcium signalingDiacylglycerol kinasePolyunsaturated fatty acidProstaglandins, Leukotrienes and Essential Fatty Acids (PLEFA)
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Structural variations in amphiphiles: Discoidal multivalent cations

1986

Fourteen cationic multipolar amphiphiles have been synthesized with pyridinium or trimethylammonium head groups. The hydrophobic cores are planar ring systems (benzene or triphenylene) to which two, three, four, or six decylene or undecylene alkyl chains are attached by ester linkages. The hydrophilic head groups are bound to the outer ends of the alkyl chains.

chemistry.chemical_classificationPolymers and PlasticsStereochemistryChemistryCationic polymerizationTriphenyleneRing (chemistry)Micellechemistry.chemical_compoundColloid and Surface ChemistryLiquid crystalPolymer chemistryAmphiphileMaterials Chemistrylipids (amino acids peptides and proteins)PyridiniumPhysical and Theoretical ChemistryAlkylColloid & Polymer Science
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Polymerizable phospholipid analogues--new stable biomembrane and cell models.

1980

chemistry.chemical_classificationPolymersCellPhospholipidBiological membraneMembranes ArtificialGeneral MedicineGeneral ChemistryPolymerModels BiologicalCatalysischemistry.chemical_compoundmedicine.anatomical_structurechemistrymedicineBiophysicsPhospholipidsAngewandte Chemie (International ed. in English)
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Organic derivatives of mercury and tin as promoters of membrane lipid peroxidation.

2008

The toxicity mechanisms of mercury and tin organic derivatives are still under debate. Generally the presence of organic moieties in their molecules makes these compounds lipophilic and membrane active species. The recent results suggest that Hg and Sn compounds deplete HS-groups in proteins, glutathione and glutathione-dependent enzymatic systems; this process also results in the production of reactive oxygen species (ROS), the enhancement of membrane lipids peroxidation and damage of the antioxidative defence system. The goal of this review is to present recent results in the studies oriented towards the role of organomercury and organotin compounds in the xenobiotic-mediated enhancement …

chemistry.chemical_classificationReactive oxygen specieslcsh:BiotechnologyRadicalMembrane lipidsOrganic Chemistrychemistry.chemical_elementNanotechnologyGlutathioneBiochemistryCombinatorial chemistrylcsh:QD146-197Mercury (element)Inorganic Chemistrychemistry.chemical_compoundMembranechemistrylcsh:TP248.13-248.65lcsh:Inorganic chemistryOrganomercuryTinResearch ArticleBioinorganic chemistry and applications
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