Search results for "Ethylene Oxide"

showing 10 items of 163 documents

Enhancement of the Mutagenicity of Ethylene Oxide and Several Directly Acting Mutagens by Human Erythrocytes and its Reduction by Xenobiotic Interact…

1999

According to the present state of knowledge mutagenicity or genotoxicity of the ulti mate genotoxic agents ethylene oxide or styrene oxide cannot be increased by further me tabolism. However, in the present study we demonstrate that mutagenicity of several ultimate genotoxic substances is increased by human erythrocytes. For instance mu tagenicity of mafosfamide, N-nitroso-N-methylurea, ethylene oxide, and styrene oxide to Salmonella typhimurium TA 1535 was increased 5.5-, 5.1-, 2.7-, and 2.3-fold, respectively, by addition of human erythrocyte homogenate to the preincubation mixture in the Ames test. On the other hand, the mutagenicity of cumene hydroperoxide, benzo[a]pyrene-4,5-oxide, and…

Ethylene oxidemedicine.disease_causeAmes testchemistry.chemical_compoundchemistryBiochemistryMafosfamideCumene hydroperoxideStyrene oxidemedicineHuman erythrocytesOrganic chemistryXenobioticGenotoxicity
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Glycidyl Tosylate: Polymerization of a “Non‐Polymerizable” Monomer permits Universal Post‐Functionalization of Polyethers

2019

Abstract Glycidyl tosylate appears to be a non‐polymerizable epoxide when nucleophilic initiators are used because of the excellent leaving group properties of the tosylate. However, using the monomer‐activated mechanism, this unusual monomer can be copolymerized with ethylene oxide (EO) and propylene oxide (PO), respectively, yielding copolymers with 7–25 % incorporated tosylate‐moieties. The microstructure of the copolymers was investigated via in situ 1H NMR spectroscopy, and the reactivity ratios of the copolymerizations have been determined. Quantitative nucleophilic substitution of the tosylate‐moiety is demonstrated for several examples. This new structure provides access to a librar…

Ethylene oxidering-opening polymerization010405 organic chemistryCommunicationLeaving groupEpoxideGeneral Chemistry010402 general chemistry01 natural sciencesRing-opening polymerizationCommunicationsCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationpolyetherPolymer chemistryCopolymerNucleophilic substitutionRing‐Opening Polymerizationfunctionalizationpoly(ethylene oxide)poly(propylene oxide)Angewandte Chemie International Edition
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Introducing an amine functionality at the block junction of amphiphilic block copolymers by anionic polymerization strategies

2011

A series of block copolymers bearing a single amino in-chain functionality was synthesized via anionic polymerization of styrene and ethylene oxide. By means of both a conventional and a continuous setup, living polystyrene was quantitatively end functionalized with an oxirane (DBAG) prior to the polymerization of the poly(ethylene oxide) segment. The in-chain amine was conjugated with a fluorescent dye.

Ethylene oxidetechnology industry and agricultureMetals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsStyrenechemistry.chemical_compoundAnionic addition polymerizationchemistryPolymerizationPolymer chemistryAmphiphileMaterials ChemistryCeramics and CompositesCopolymerLiving polymerizationPolystyreneChemical Communications
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Amino Functional Poly(ethylene glycol) Copolymers via Protected Amino Glycidol

2010

The synthesis of poly(ethylene glycol) (PEG) copolymers with multiple amino functionalities within the chain is described, relying on an epoxide comonomer bearing a protected amino group. N,N-dibenzyl amino glycidol (DBAG) and ethylene oxide (EO) were copolymerized via anionic polymerization, leading to well-defined polymers with varied comonomer content and low polydispersities (Mw/Mn in the range of 1.1 to 1.2). Subsequent hydrogenolysis with Pearlman’s catalyst afforded poly(ethylene glycol-co-amino glycerol)s (PEG-co-PAG) with a precisely adjusted number of randomly incorporated amino groups in the range of 2−15%. For the first time, the kinetics of an EO copolymerizations have has been…

EthylenePolymers and PlasticsEthylene oxideComonomerOrganic Chemistrytechnology industry and agricultureGlycidolEpoxideInorganic Chemistrychemistry.chemical_compoundAnionic addition polymerizationMonomerchemistryPolymer chemistryMaterials ChemistryOrganic chemistryEthylene glycolMacromolecules
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Gelchromatographie, 12. Gelchromatographisches Verhalten von Polyvinylalkoholgelen

1975

Durch Hydrolyse von Copolymeren aus Vinylacetat und 1,4-Bis(vinyloxy)butan werden vernetzte Polyvinylalkoholgele hergestellt und ihre Eignung als hydrophile stationare Phase bei gelchromatographischen Trennungen mit Dextranen, Poly(athylenoxid)en und Proteinen als Testsubstanzen gepruft. Die Gele sind druck- und biostabil und zeigen keine storende Adsorption. Je nach Herstellungsbedingungen werden Ausschlusmolekulargewichte bis zu 106 erzielt. Hydrolysis of copolymers from vinyl acetate and 1,4-bis(vinyloxy)butane results in crosslinked poly(vinyl alcohol) gels. Their applicability as hydrophilic stationary phase in gel permeation chromatography is investigated using dextranes, poly(ethylen…

Gel permeation chromatographychemistry.chemical_compoundVinyl alcoholHydrolysisAdsorptionchemistryEthylene oxidePolymer chemistryVinyl acetateCopolymerHydrophileDie Makromolekulare Chemie
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Rapid Access to Polyfunctional Lipids with Complex Architecture via Oxyanionic Ring-Opening Polymerization

2011

Polymer-coated liposomes, particularly poly(ethylene glycol) (PEG)-substituted liposomes, have emerged as long-circulating carrier systems for drug delivery and diagnostic purposes. A rapid synthesis of three different types of multifunctional lipids with structurally diverse hydrophilic, polyether-based architectures via one- or two-pot approaches is described. Architectural variation is achieved by the combination of different oxyanionic polymerization strategies and various glycidyl ether building units. Branched polyglycerol lipids have been prepared via cholesterol- or 1,2-bis-n-alkyl glyceryl ether-initiated, oxyanionic ring-opening polymerization (ROP) of protected glycidyl ethers an…

Hyperbranched PolyglycerolsPolymers and PlasticsEffectively ProlongRing-opening polymerizationMicelleCirculation TimeInorganic Chemistrychemistry.chemical_compoundAmphiphilePolymer chemistryMaterials ChemistryCopolymerOrganic chemistryPoly(Ethylene Glycol) CopolymersSolid TumorsCationic-PolymerizationDrug-Delivery SystemsOxide) OligomersEthylene oxideOrganic ChemistryCationic polymerizationEnd-groupchemistryPolymerizationBlock-CopolymersIn-Vivo
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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Binding of Short Alkyl Chain Surfactants to the (Ethylene oxide)13−(Propylene oxide)30−(Ethylene oxide)13and (Ethylene oxide)75−(Propylene oxide)30−(…

2002

The enthalpy of transfer (ΔHt) of neutral copolymers, at a fixed and low concentration ca. 10-3 mol kg-1, from water to the aqueous surfactant solutions as a function of the surfactant concentration (fSmS) was determined at 25 °C. The surfactants studied are sodium octanoate, sodium decanoate, N-octylpyridinium chloride (OPC), and N,N-dimethyloctylamine-N-oxide (ODAO). The copolymers are (ethylene oxide)13−(propylene oxide)30−(ethylene oxide)13 (L64) and (ethylene oxide)75−(propylene oxide)30−(ethylene oxide)75 (F68). The two copolymers show different hydrophilic−hydrophobic ratios, the larger being for F68. As a general feature, the shape of the ΔHt vs fSmS curve depends on the nature of t…

Isothermal microcalorimetrychemistry.chemical_classificationAqueous solutionPolymers and PlasticsEthylene oxideOrganic ChemistryInorganic chemistryChlorideInorganic Chemistrychemistry.chemical_compoundchemistryPulmonary surfactantMaterials ChemistrymedicineCopolymerPropylene oxideAlkylmedicine.drugMacromolecules
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Small Angle Neutron Scattering, X-ray Diffraction, Differential Scanning Calorimetry, and Thermogravimetry Studies to Characterize the Properties of …

2009

Nanocomposites based on laponite RD and (ethylene oxide)98(propylene oxide)67(ethylene oxide)98 (F127)triblock copolymer or poly(ethylene) glycol 2000 (PEG2000) were prepared by using the melting method. Small-angle neutron scattering and the X-ray diffraction experiments provided insights into the organization of the laponite RD dispersed in the macromolecular matrix over a wide length scale. SANS data analysis by means of a fractal law evidenced the formation of clusters of laponite RD at long correlation distance. The single laponite RD particles and the lamellar structure of F127 were described in the shorter length scale. Finally, the crystalline structure of the macromolecule was obse…

Length scaleTGAMaterials scienceEthylene oxidenanocompositepoly(ethylene oxide)poly(propylene oxide)poly(ethylene oxide)SANSXRDAnalytical chemistrypoly(ethylene)glycol 2000laponite RDNeutron scatteringSmall-angle neutron scatteringSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsDSCThermogravimetrychemistry.chemical_compoundGeneral EnergyDifferential scanning calorimetrychemistryX-ray crystallographyLamellar structurePhysical and Theoretical Chemistry
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Multifunctional Poly(ethylene glycol)s

2011

In the rapidly evolving multidisciplinary field of polymer therapeutics, tailored polymer structures represent the key constituent to explore and harvest the potential of bioactive macromolecular hybrid structures. In light of the recent developments for anticancer drug conjugates, multifunctional polymers are becoming ever more relevant as drug carriers. However, the potentially best suited polymer, poly(ethylene glycol) (PEG), is unfavorable owing to its limited functionality. Therefore, multifunctional linear copolymers (mf-PEGs) based on ethylene oxide (EO) and appropriate epoxide comonomers are attracting increased attention. Precisely engineered via living anionic polymerization and d…

LymphomapolyethersNanotechnologyAntineoplastic AgentsPolyethylene glycolMolecular-WeightCatalysisPolyethylene Glycolschemistry.chemical_compoundepoxidesCopolymerOrganic chemistryAnimalsLiving anionic polymerizationchemistry.chemical_classificationWeight Hyperbranched PolyglycerolsDrug CarriersDrug-Delivery SystemsEthylene oxidepoly(ethylene glycol)Ethylene-OxideGene Transfer TechniquesPolymer TherapeuticsGeneral ChemistryPolymermultivalencybioconjugatesPendant Amino-GroupsPolyethylene-GlycolchemistryPolymerizationAnionic Peg DerivativesDoxorubicinBlock-CopolymersCisplatinIn-VivoDrug carrierPeptidesEthylene glycol
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