Search results for "molecular weight"

showing 10 items of 366 documents

Biocompatibility of alginates for grafting: impact of alginate molecular weight.

2003

Optimising microencapsulation technology towards the effective clinical transplantation has created the need for highly biocompatible alginates. Therefore, in this study the biocompatibility of different beads prepared from alginates with varying average molecular weight was examined. In some experiments the beads were covered with a multilayer membrane surrounded by an alginate layer. First of all, we found that beads made of a lower weight average alginate elicted a much stronger fibrotic response compared to beads made of a higher weight average alginate (LV-alginate > MV-alginate). The results were confirmed by the observation that the extent of tissue fibrosis was significantly increas…

BiocompatibilityMolecular massChemistryAlginatesDrug CompoundingBiomedical EngineeringBiocompatible MaterialsGraftingBiocompatible materialFibrosisMicrospheresRatsTransplantationMolecular WeightRats Sprague-DawleyViscosityChemical engineeringImplants ExperimentalTissue fibrosisMaterials TestingMolar mass distributionAnimalsBiotechnologyBiomedical engineeringArtificial cells, blood substitutes, and immobilization biotechnology
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Modifying the body distribution of HPMA-based copolymers by molecular weight and aggregate formation.

2011

There is a recognized need to create well-defined polymer probes for in vivo and clinical positron emission tomography (PET) imaging to guide the development of new generation polymer therapeutics. Using the RAFT polymerization technique in combination with the reactive ester approach, here we have synthesized well-defined and narrowly distributed N-(2-hydroxypropyl)methacrylamide homopolymers (pHPMA) (P1* and P2*) and random HPMA copolymers consisting of hydrophilic HPMA and hydrophobic lauryl methacrylate comonomers (P3* and P4*). The polymers had molecular weights below (P1* and P3*) and above the renal threshold (P2* and P4*). Whereas the homopolymers dissolve in isotonic solution as in…

BiodistributionPolymers and PlasticsPolymersBioengineeringFluorescence correlation spectroscopyBiomaterialschemistry.chemical_compoundPolymer chemistryMaterials ChemistryCopolymerMethacrylamideMoleculeAnimalsReversible addition−fragmentation chain-transfer polymerizationTissue Distributionchemistry.chemical_classificationMolecular StructureStereoisomerismPolymerRatsMolecular WeightchemistryCritical micelle concentrationPositron-Emission TomographyMethacrylatesRadiopharmaceuticalsBiomacromolecules
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Molecular Cloning, Heterologous Expression, and Characterization of Ornithine Decarboxylase from Oenococcus oeni

2011

International audience; Ornithine decarboxylase (ODC) is responsible for the production of putrescine, the major biogenic amine found in wine. Oenococcus oeni is the most important lactic acid bacterium in the winemaking process and is involved in malolactic fermentation. We report here the characterization of ODC from an O. oeni strain isolated from wine. Screening of 263 strains isolated from wine and cider from all over the world revealed that the presence of the odc gene appears to be strain specific in O. oeni. After cloning, heterologous expression in Escherichia coli, and characterization, the enzyme was found to have a molecular mass of 85 kDa and a pI of 6.2 and revealed maximal ac…

Biogenic Aminesgenetic structuresWinemedicine.disease_causeMicrobiologyOrnithine decarboxylaseOrnithine decarboxylaseIndustrial Microbiology03 medical and health scienceschemistry.chemical_compoundmedicineMalolactic fermentationHumans[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyEscherichia coliOenococcus030304 developmental biologyOenococcus oeniWinemaking0303 health sciencesCadaverinebiology030306 microbiologyTemperaturefood and beveragesHydrogen-Ion Concentrationbiology.organism_classificationMolecular WeightKineticschemistryBiochemistryFermentationPutrescineHeterologous expressionOenococcus oeniFood ScienceJournal of Food Protection
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Sedimentation properties of chitosomal chitin synthetase from the wild-type strain and the 'slime' variant of Neurospora crassa.

1989

Marked differences in the pattern of sedimentation of cellular structures were observed after isopycnic centrifugation of crude cell-free preparations from the Neurospora crassa wall-less 'slime' variant and mycelial wild-type strain. Kinetic studies of particle sedimentation showed that the various types of subcellular components, as revealed by turbidity, UV absorption, polypeptide patterns, and chitin synthetase activity determinations, sediment independently of one another. An important feature was the finding that chitin synthetase from 'slime' peaked at a median specific gravity of 1.1201 +/- 0.0036, whereas that from wild-type strain sedimented at a higher buoyant density (specific g…

BiophysicsCentrifugation IsopycnicBiochemistryNeurospora crassaCell wallchemistry.chemical_compoundChitinCentrifugation Density GradientMolecular BiologyPolyacrylamide gel electrophoresisSpecific GravityDifferential centrifugationChitin SynthaseOrganellesbiologyStrain (chemistry)Neurospora crassafungiCrassaGenetic VariationSedimentationbiology.organism_classificationcarbohydrates (lipids)Molecular WeightKineticsMicroscopy ElectronNeurosporaBiochemistrychemistryGlucosyltransferasesElectrophoresis Polyacrylamide GelSpectrophotometry UltravioletBiochimica et biophysica acta
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Techniques to measure sorption and migration between small molecules and packaging. A critical review

2015

The mass transfer parameters diffusion and sorption in food and packaging or between them are the key parameters for assessing a food product's shelf-life in reference to consumer safety. This has become of paramount importance owing to the legislations set by the regulated markets. The technical capabilities that can be exploited for analyzing product–package interactions have been growing rapidly. Different techniques categorized according to the state of the diffusant (gas or liquid) in contact with the packaging material are emphasized in this review. Depending on the diffusant and on the analytical question under review, the different ways to study sorption and/or migration are present…

Bunsen solubility coefficientComputer scienceFood ContaminationNanotechnology[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainpartition coefficientConsumer safetyDiffusionsolubility coefficientHumansMeasure (data warehouse)sorptionNutrition and Dieteticsbusiness.industrySorptionChemical industrypackaging polymers[SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry Molecular Biology/Biomolecules [q-bio.BM]Molecular WeightFood packagingAdsorptionBiochemical engineeringbusinessPlastics[SDV.AEN]Life Sciences [q-bio]/Food and NutritionAgronomy and Crop Sciencefood packagingFood ScienceBiotechnologyJournal of the Science of Food and Agriculture
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Cell-cell and cell-collagen interactions influence gelatinase production by human breast-carcinoma cell line 8701-BC

1995

We previously produced evidence that the human mammary-carcinoma cell line 8701-BC expresses several metalloproteinases (MMP-1, -2, -9, and -10) and their tissue inhibitors. In order to obtain a better understanding of the environmental control over gelatinolytic activities, we have tested the enzyme production of 8701-BC cells, at time intervals after plating on different collagen substrates, i.e., types I, III, IV, V and OF/LB, used as films in culture dishes. Proteinase activities, released in the conditioned culture media, were tested by zymography on SDS-PAGE, and by quantificative analyses, using 14C carboxy-methylated transferrin as substrate in a liquid incubation medium. Enzymatic …

Cancer ResearchConfluencyKunitz STI protease inhibitorBreast NeoplasmsCell CommunicationBiologyTrypsinCulture MediaMolecular WeightOncologyBiochemistryCell–cell interactionGelatinasesCell cultureEndopeptidasesTumor Cells CulturedmedicineHumansGelatinaseSerine Proteinase InhibitorsZymographyCollagenCell Divisionmedicine.drugInternational Journal of Cancer
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Cytoskeletal differences between human neuroendocrine tumors: A cytoskeletal protein of molecular weight 46,000 distinguishes cutaneous from pulmonar…

1985

The cytoskeletons of various human neuroendocrine (NE) tumors were analyzed immunohistochemically using antibodies against intermediate-filament (IF) proteins as well as by two-dimensional gel electrophoresis of proteins from microdissected tissue samples. All of the tumors studied were found to contain cytokeratin filaments and are therefore referred to as 'NE tumors of the epithelial type'. In addition, neurofilaments were found in most cutaneous and some pulmonary NE tumors, as well as in medullary carcinomas of the thyroid and in pancreatic islet cell tumors. The neurofilament staining was frequently concentrated in cytoplasmic IF aggregates. Gel-electrophoretic analyses showed that all…

Cancer ResearchPathologymedicine.medical_specialtyLung NeoplasmsSkin NeoplasmsNeurofilamentCarcinoid TumorHistogenesisBiologyNeuroendocrine tumorsDiagnosis DifferentialCytokeratinIntestinal NeoplasmsKeratinmedicineCarcinomaHumansThyroid NeoplasmsCarcinoma Small CellMolecular Biologychemistry.chemical_classificationThyroidCell Biologymedicine.diseaseNeoplasm ProteinsMolecular WeightPancreatic NeoplasmsCytoskeletal Proteinsmedicine.anatomical_structurechemistryImmunologyPancreasDevelopmental BiologyDifferentiation
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Optimal duration of low molecular weight heparin for the treatment of cancer-related deep vein thrombosis. The ”CANCER DACUS” study

2014

Purpose We evaluated the role of residual vein thrombosis (RVT) to assess the optimal duration of anticoagulants in patients with cancer who have deep vein thrombosis (DVT) of the lower limbs. Patients and Methods Patients with active cancer and a first episode of DVT treated with low molecular weight heparin (LMWH) for 6 months were eligible. Patients were managed according to RVT findings: those with RVT were randomly assigned to continue LMWH for an additional 6 months (group A1) or to discontinue it (group A2), and patients without RVT stopped LMWH (group B). The primary end point was recurrent venous thromboembolism (VTE) during the 1 year after disconinuation of LMWH, and the secondar…

Cancer Researchmedicine.medical_specialtymedicine.drug_classDeep veinPopulationLow molecular weight heparinSettore MED/42 - Igiene Generale E ApplicataGroup BSettore MED/15 - Malattie Del SangueInternal medicineresidual vein thrombosis low molecular weight heparin cancer patientsmedicineeducationFirst episodeeducation.field_of_studybusiness.industrylow molecular weight heparinHazard ratioantivitamin K; low molecular weight heparin; nadroparinCancermedicine.diseaseThrombosisSurgerymedicine.anatomical_structureOncologynadroparinantivitamin Kbusiness
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Multi-functional hybrid-carbon nanotubes for advanced Ultra-High Molecular Weight Polyethylene-based nanocomposites: a novel approach for stabilizati…

2015

Our results demonstrate that immobilizing stabilizing molecules on nanoparticles, and using the latter as multifunctional filler for nanocomposites, is a viable route towards to produce high-performance polymeric materials

Carbon nanotubes Ultra-High Molecular Weight Polyethylene nanocomposites stabilization
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Purification and characterization of two exopolyphosphatases from the marine sponge Tethya lyncurium

1995

Abstract Two exopolyphosphatases (exopolyphosphatase I and II; EC 3.6.1.11) which release orthophosphate from inorganic polyphosphates have been detected and purified for the first time from a marine sponge, Tethya lyncurium . Exopolyphosphatase I has a molecular mass of 45 kDa, a pH optimum of 5.0 and does not require divalent cations for activity, while exopolyphosphatase II has a molecular mass of 70 kDa, a pH optimum of 7.5 and displays optimal activity in the presence of Mg 2+ ions. Final purification of the enzymes could be achieved by affinity chromatography on polyphosphate-modified zirconia. The mode of action of both enzymes was found to be processive. Orthophosphate is the sole p…

Cations DivalentBiophysicsAdenylate kinaseBiochemistryPyrophosphateDivalentchemistry.chemical_compoundPolyphosphatesProtein purificationAnimalsMolecular BiologyExopolyphosphatasechemistry.chemical_classificationChromatographyMolecular massPolyphosphateTemperatureHydrogen-Ion ConcentrationAcid Anhydride HydrolasesPoriferaMolecular WeightKineticsEnzymechemistryBiochemistryAdenylyl Cyclase InhibitorsBiochimica et Biophysica Acta (BBA) - General Subjects
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