Search results for "gate"

showing 10 items of 1811 documents

Microbial production of biopolymers from the renewable resource wheat straw.

2014

Aims Production of poly-s-hydroxybutyrate (PHB) and the chemical basic compound lactate from the agricultural crop ‘wheat straw’ as a renewable carbon resource. Methods and Results A thermal pressure hydrolysis procedure for the breakdown of wheat straw was applied. By this means, the wheat straw was converted into a partially solubilized hemicellulosic fraction, consisting of sugar monomers, and an insoluble cellulosic fraction, containing cellulose, lignin and a small portion of hemicellulose. The insoluble cellulosic fraction was further hydrolysed by commercial enzymes in monomers. The production of PHB from the sugar monomers originating from hemicellulose or cellulose was achieved by …

PolyestersHydroxybutyratesBacillusBiodegradable PlasticsXyloseAcetatesApplied Microbiology and BiotechnologyLigninHydrolysatechemistry.chemical_compoundIndustrial MicrobiologyLigninHemicelluloseFood scienceLactic AcidCelluloseSugarCelluloseTriticumHydrolysisfood and beveragesGeneral MedicineStrawBiochemistrychemistryCellulosic ethanolBacillus megateriumBiotechnologyJournal of applied microbiology
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Non-Benzenoid Conjugated Carbocyclic Compounds. Von D. Lloyd. Elsevier, Amsterdam 1984. XVI, 431 S., geb. HFI. 262.00. – ISBN 0-444-42346-X

1985

Polymer scienceChemistryStereochemistryGeneral MedicineConjugated systemAngewandte Chemie
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18F-Radiolabeling, Preliminary Evaluation of Folate-pHPMA Conjugates via PET

2014

The synthesis of a 10.5 kDa and a 52.5 kDa polymer, based on pHPMA functionalized with tyramine for (18) F-labeling and a folate derivative as targeting moiety, is reported. FCS studies are conducted using Oregon Green-labeled conjugates. No aggregation is observed for the 10.5 kDa conjugate, but strong aggregation for the 52.5 kDa conjugate. In vivo studies are conducted using Walker-256 mammary carcinoma model to determine body distribution as function of size and especially targeting unit. These in vivo studies show a higher short time (2 h) accumulation for both conjugates in the tumor than for untargeted pHPMA, confirmed by blockade studies. The 10.5 kDa polymer accumulates with 0.46% …

Polymers and PlasticsBioengineeringTyramineWalker 256 carcinomaBiomaterialsMammary carcinomachemistry.chemical_compoundchemistryBiochemistryIn vivoMaterials ChemistryDistribution (pharmacology)MoietyBiotechnologyConjugateMacromolecular Bioscience
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Biotin-Containing Reduced Graphene Oxide-Based Nanosystem as a Multieffect Anticancer Agent: Combining Hyperthermia with Targeted Chemotherapy

2015

Among the relevant properties of graphene derivatives, their ability of acting as an energy-converting device so as to produce heat (i.e., thermoablation and hyperthermia) was more recently taken into account for the treatment of solid tumors. In this pioneering study, for the first time, the in vitro RGO-induced hyperthermia was assessed and combined with the stimuli-sensitive anticancer effect of a biotinylated inulin-doxorubicin conjugate (CJ-PEGBT), hence, getting to a nanosystem endowed with synergic anticancer effects and high specificity. CJ-PEGBT was synthesized by linking pentynoic acid and citraconic acid to inulin. The citraconylamide pendants, used as pH reversible spacer, were …

Polymers and PlasticsBiotinAntineoplastic AgentsBreast NeoplasmsBioengineeringlaw.inventionBiomaterialschemistry.chemical_compoundDrug Delivery SystemslawMaterials ChemistrymedicineHumansMoietyOrganic chemistryDoxorubicinChemistryGrapheneInulinHyperthermia InducedHydrogen-Ion ConcentrationCitraconic acidgraphene drug delivery hypertermia anticancer inulinCombinatorial chemistryDoxorubicinSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiotinylationDrug deliveryMCF-7 CellsNanoparticlesNanomedicineFemaleGraphiteConjugatemedicine.drugBiomacromolecules
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Amphiphilic Copolymers Based on Poly[(hydroxyethyl)-d,l-aspartamide]: A Suitable Functional Coating for Biocompatible Gold Nanostars

2013

Novel amphiphilic copolymers have been synthesized based on a biocompatible poly(hydroxyethylaspartamide) (PHEA) backbone, bearing both anchoring groups for gold nanoparticles, such as thiols and disulfide, and conjugable moieties, such as amino groups, the latter as points suitable for appending further functional agents. The strategy was to functionalize α,β-poly[(N-2- hydroxyethyl)-d,l-aspartamide] (PHEA) with PEG2000-NH2 and with ethylenediamine (EDA) obtaining a partially pegylated copolymer with a large number of pendant primary amino groups. A fraction of the latter was conjugated with molecules bearing terminal thiol moieties such as 12-mercaptododecanoic acid (MDA) and disulfide gr…

Polymers and PlasticsCell SurvivalMetal NanoparticlesBioengineeringEthylenediamineengineering.materialConjugated systemPolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundCoated Materials BiocompatibleCoatingCell Line TumorMaterials TestingAmphiphilePolymer chemistryMaterials ChemistryCopolymerHumansMoleculePoly(hydroxyethyl)-DL-aspartamideParticle Sizechemistry.chemical_classificationAmphiphilic copolymersgold nanostarlipoic acidEthylenediamineschemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoColloidal goldThiolengineeringGoldPeptidesgold nanoparticleBiomacromolecules
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J-aggregates prepared by adsorption at monolayer/water interfaces

1991

By adsorption of anionic cyanine dyes at positivly charged lipid monolayers large J-aggregates are formed. Absorption and fluorescence spectra are measured at the air/water interface during the crystallization process. The influence of the lipid/dye interaction on the aggregate structure is studied for two different systems. It is shown that the aggregate structure can be improved by growing crystals from a seed.

Polymers and PlasticsChemistryOrganic ChemistryInorganic chemistryCrystal growthCondensed Matter Physicslaw.inventionchemistry.chemical_compoundAdsorptionChemical engineeringlawAggregate structureMonolayerMaterials ChemistryCrystallizationCyanineAbsorption (chemistry)J-aggregateMakromolekulare Chemie. Macromolecular Symposia
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Covalently Binding of Bovine Serum Albumin to Unsaturated Poly(Globalide-Co-ε-Caprolactone) Nanoparticles by Thiol-Ene Reactions.

2019

When nanoparticles (NPs) are introduced to a biological fluid, different proteins (and other biomolecules) rapidly get adsorbed onto their surface, forming a protein corona capable of giving to the NPs a new "identity" and determine their biological fate. Protein-nanoparticle conjugation can be used in order to promote specific interactions between living systems and nanocarriers. Non-covalent conjugates are less stable and more susceptible to desorption in biological media, which makes the development of engineered nanoparticle surfaces by covalent attachment an interesting topic. In this work, the surface of poly(globalide-co-e-caprolactone) (PGlCL) nanoparticles containing double bonds i…

Polymers and PlasticsNanoparticleBioengineering02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundLactonesMaterials ChemistryAnimalsHumansBovine serum albuminParticle SizeCaproateschemistry.chemical_classificationbiologyThiol-ene reactionBiomoleculeSerum Albumin Bovine021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryCovalent bondbiology.proteinNanoparticlesCattleNanocarriers0210 nano-technologyCaprolactoneBiotechnologyConjugateHeLa CellsMacromolecular bioscience
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HPMA-Based Nanoparticles for Fast, Bioorthogonal iEDDA Ligation

2019

Contains fulltext : 216143.pdf (Publisher’s version ) (Open Access) Fast and bioorthogonally reacting nanoparticles are attractive tools for biomedical applications such as tumor pretargeting. In this study, we designed an amphiphilic block copolymer system based on HPMA using different strategies to introduce the highly reactive click units 1,2,4,5-tetrazines (Tz) either at the chain end (Tz-CTA) or statistical into the hydrophobic block. This reactive group undergoes a rapid, bioorthogonal inverse electron-demand Diels-Alder reaction (iEDDA) with trans-cyclooctenes (TCO). Subsequently, this polymer platform was used for the preparation of different Tz-covered nanoparticles, such as micell…

Polymers and PlasticsNanoparticleBioengineeringFluorescence correlation spectroscopy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesMicelleArticleBiomaterialsAmphiphileMaterials ChemistryCopolymerBenzene DerivativesColloidsMicellesPretargetingAza CompoundsCycloaddition ReactionChemistryOther Research Radboud Institute for Health Sciences [Radboudumc 0]021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesCross-Linking ReagentsMethacrylatesNanoparticlesClick ChemistryBioorthogonal chemistry0210 nano-technology
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"A versatile post-polymerization modification method for polyglutamic acid: synthesis of orthogonal reactive polyglutamates and their use in ""click …

2013

In this article we describe a versatile methodology for the synthesis of polyglutamic acid (PGA) derivatives bearing orthogonal reactive sites. The reactive groups enable selective conjugation chemistry by copper catalyzed azide-alkyne coupling (CuAAC). PGA was derived in aqueous media as well as in organic media using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl morpholinium chloride (DMTTM) salts. The spectra of attached chemical moieties ranges from simple PEGylation with 2,5,8,11,14,17,20-heptaoxadocosan-22-amine (mEG(6)NH2) to the incorporation of propargylamine, 11-azido-3,6,9-trioxaundecan-1-amine (NH2-EG(2)N-3), and 20-azido-3,6,9,12,15,18-hexaoxaicosan-1-amine (NH2-EG(6)N-3). Here…

Polymers and PlasticsOrganic ChemistryPolyglutamic acidBioengineering02 engineering and technologyConjugated system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCombinatorial chemistryOrganic mediaChloride0104 chemical scienceschemistry.chemical_compoundchemistryPEGylationClick chemistrymedicineOrganic chemistrySurface modification0210 nano-technologyPost polymerizationmedicine.drug
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HPMC-salicylate conjugates as macromolecular prodrugs: Design, characterization, and nano-rods formation

2009

The design, characterization, and nano-rods formation of hydroxypropylmethylcellulose (HPMC)-salicylate conjugates as macromolecular prodrugs, was described. HPMC, obtained from Zhejiang Zhongbao Imp and Exp Corp, was dried under vacuum at 110°C for 8 hr. Nanoparticles were prepared using dialysis process in which 170 mg of HPMC-salicylate sample was dissolved in 5 mL of purified DMSO and was dialyzed against distilled water for 4 days. HPMC-salicylic acid conjugates reveal the absence of sulfur in all of the samples showing that there is no introduction to tosylate groups either covalently bounded or as an impurity.

Polymers and PlasticsOrganic Chemistrytechnology industry and agricultureChemical modificationProdrugbody regionschemistry.chemical_compoundchemistryDistilled waterCovalent bondMaterials ChemistryOrganic chemistrySelf-assemblyDrug carrierSalicylic acidNuclear chemistryConjugateJournal of Polymer Science Part A: Polymer Chemistry
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