Search results for "geeli"

showing 10 items of 23 documents

In situ formation of steroidal supramolecular gels designed for drug release

2013

In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macroand microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with…

In situMagnetic Resonance SpectroscopykolesteroliImineSupramolecular chemistryPharmaceutical ScienceArticleChloroquinolinolsAnalytical ChemistryDelayed-Action Preparationslcsh:QD241-441chemistry.chemical_compoundgeeliDrug Delivery Systemslcsh:Organic chemistryDrug DiscoveryPolymer chemistryMoleculeddc:530Physical and Theoretical Chemistryta116drug releaseOrganic ChemistryorganogelcholesterolNuclear magnetic resonance spectroscopyacid-responsiveHydrogen-Ion ConcentrationchemistryChemistry (miscellaneous)in situ gelationDelayed-Action PreparationsDrug deliveryDrug releaseMolecular Medicineorganogel; acid-responsive; cholesterol; <i>in situ</i> gelation; drug releaseGels
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Systematic Modulation of the Supramolecular Gelation Properties of Bile Acid Alkyl Amides

2018

The self-assembly properties of nine low-molecular-weight gelators (LMWGs) based on bile acid alkyl amides were studied in detail. Based on the results, the number of hydroxyl groups attached to the steroidal backbone plays a major role in the gelation, although the nature of the aliphatic side chain also modulates the gelation abilities. Of the 50 gel systems studied, 35 are based on lithocholic acid and 15 on cholic acid derivatives. The deoxycholic acid derivatives did not form any gels. The gelation occurred primarily in aromatic solvents and the gels manifested typical fibrous or spherical morphologies. The 13C cross-polarized magic angle spinning (CPMAS) NMR spectra measured on the cr…

Lithocholic acidSupramolecular chemistry02 engineering and technology010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAmidebile acid amidesPolymer chemistrysupramolekulaarinen kemiaSide chainMagic angle spinningNMR-spektroskopiata116AlkylX-ray crystallographygeelitchemistry.chemical_classificationintermolecular interactionsOrganic ChemistryDeoxycholic acidsupramolecular gelsCholic acidGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryamidit0210 nano-technologyröntgenkristallografiaChemistry – A European Journal
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Gelation behavior of 5-chloro-8-hydroxyquinoline, an antituberculosis agent, in aqueous alcohol solutions

2012

It was shown that 5-chloro-8-hydroxyquinoline, an antituberculosis agent, gels aqueous alcohol solutions efficiently. Thermal stability and gel-to-sol transition temperature of 1% gel in CD3OD/D2O (2:1) was studied by 1H-NMR. Fibrous structures of four xerogels have been characterized by scanning electron microscope. peerReviewed

Microbiology (medical)gelScanning electron microscope5-kloori-8-hydroksikinoliinigel; 5-chloro-8-hydroxyquinoline; <em>Mycobacterium </em><em>tuberculosis</em>gelationBiochemistryMicrobiologyArticle5-chloro-8-hydroxyquinolinechemistry.chemical_compoundOrganic chemistryPharmacology (medical)Thermal stabilityGeneral Pharmacology Toxicology and Pharmaceuticsta116Aqueous alcoholgeelin muodostusTransition temperature5-chloro-8-hydoxyquinolinelcsh:RM1-950Antituberculosis agent8-HydroxyquinolineMycobacterium tuberculosisInfectious Diseaseslcsh:Therapeutics. PharmacologychemistryNuclear chemistryAntibiotics
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Caffeine as a Gelator

2016

Caffeine (a stimulant) and ethanol (a depressant) may have opposite effects in our body, but under in vitro conditions they can “gel” together. Caffeine, being one of the widely used stimulants, continued to surprise the scientific community with its unprecedented biological, medicinal and physicochemical properties. Here, we disclose the supramolecular self-assembly of anhydrous caffeine in a series of alcoholic and aromatic solvents, rendering a highly entangled microcrystalline network facilitating the encapsulation of the solvents as illustrated using direct imaging, microscopy analysis and NMR studies. Peer reviewed

Polymers and Plasticsmedicine.drug_classSupramolecular chemistryBioengineeringDirect imaging02 engineering and technology010402 general chemistry01 natural sciencessupramolecular chemistrylcsh:ChemistryBiomaterialschemistry.chemical_compoundAnhydrous caffeinelcsh:General. Including alchemySupramolecularlcsh:Inorganic chemistrysupramolekulaarinen kemiamedicineOrganic chemistrylcsh:Scienceta116caffeinegeelitsolid state NMREthanolta114ChemistryCommunicationOrganic Chemistry021001 nanoscience & nanotechnologygelslcsh:QD146-1970104 chemical sciences3. Good healthMicrocrystallinelcsh:QD1-999kofeiiniAromatic solventslcsh:QDepressant0210 nano-technologyCaffeinelcsh:QD1-65Gels Caffeine SupramolecularGels
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Reactive Self-Assembly and Specific Cellular Delivery of NCO-sP(EO-stat-PO)-Derived Nanogels

2018

This study presents the reactive self-assembly of isocyanate functional and amphiphilic six-arm, star-shaped polyether prepolymers in water into nanogels. Intrinsic molecular amphiphilicity, mainly driven by the isophorone moiety at the distal endings of the star-shaped molecules, allows for the preparation of spherical particles with an adjustable size of 100-200 nm by self-assembly and subsequent covalent cross-linking without the need for organic solvents or surfactants. Covalent attachment of a fluorescence dye and either the cell-penetrating TAT peptide or a random control peptide sequence shows that only TAT-labeled nanogels are internalized by HeLa cells. The nanogels thus specifical…

Polymers and Plasticsta221Bioengineering02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiokemia solu- ja molekyylibiologia - Biochemistry cell and molecular biologyBiomaterialschemistry.chemical_compoundnanogelsDrug Delivery SystemsAmphiphileMaterials ChemistryHumansPolyethyleneimineMoleculeMoietynanopolymeeritreactive self-assemblyPeptide sequenceFluorescent DyesIsophoronegeelitta1182nanobiotekniikka021001 nanoscience & nanotechnologyIsocyanate0104 chemical scienceschemistryCovalent bondBiophysicsNanoparticlesSelf-assembly0210 nano-technologyHeLa CellsBiotechnology
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Infinite coordination polymer networks metallogelation of aminopyridine conjugates and in situ silver nanoparticle formation

2018

Herein we report silver(i) directed infinite coordination polymer network (ICPN) induced self-assembly of low molecular weight organic ligands leading to metallogelation. Structurally simple ligands are derived from 3-aminopyridine and 4-aminopyridine conjugates which are composed of either pyridine or 2,2'-bipyridine cores. The cation specific gelation was found to be independent of the counter anion, leading to highly entangled fibrillar networks facilitating the immobilization of solvent molecules. Rheological studies revealed that the elastic storage modulus (G') of a given gelator molecule is counter anion dependent. The metallogels derived from ligands containing a bipyridine core dis…

STABILIZATIONSilverCoordination polymerNanoparticleMetal Nanoparticles02 engineering and technologyorganometalliyhdisteet010402 general chemistry01 natural sciencesSilver nanoparticlePolymerizationchemistry.chemical_compoundBipyridinePyridineorganometallic compoundsMoleculePARTICLESCRYSTAL-STRUCTURES4-Aminopyridinepolymeeritta116GELSpolymersgeelitHYBRID MATERIALSta114General Chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsGELATION0104 chemical sciencesCrystallographyREDUCTIONCross-Linking ReagentschemistryPolymerizationMETALLUMINESCENCEPHASE-TRANSITIONCoordination polymerizationnanohiukkasetnanoparticles0210 nano-technologyRheologySOFT MATTER
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Subcomponent Self-Assembly A Quick Way to New Metallogels

2013

Subcomponent self-assembly, introduced by the Nitschke group,[1] is a process which allow complex structures to be generated from simple building blocks (generally aldehydes and amines). In this bottom-up approach, the building blocks spontaneously self-assemble around templates (usually metal ions) leading to a simultaneous covalent (C=N) and dative (N– metal) bonds formation. The method has been successfully used to construct well-defined metal-organic macrocycles, helicates, catenanes, rotaxanes, grids,[2] and cages.[3] Our field of interest lies not in building-up of defined structures but in designing gelator molecules for a formation of supramolecular gels as functional nanomaterials.…

SUPRAMOLECULAR GELSMetal ions in aqueous solutionta221GELATORSSupramolecular chemistryNanoparticleNanotechnologymetallogeelimultistimuli responsive010402 general chemistrySmart material01 natural sciencesCatalysisMOLECULESMoleculeta116ta218ta214ta114010405 organic chemistryChemistryIN-SITUOrganic ChemistryGeneral Chemistryself-assemblygelsGELATION0104 chemical sciencesin situ gelationMETALnanoparticlesSelf-assemblymetallogelCHEMISTRY: A EUROPEAN JOURNAL
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Bioactive glass ions induce efficient osteogenic differentiation of human adipose stem cells encapsulated in gellan gum and collagen type I hydrogels

2019

Abstract Background Due to unmet need for bone augmentation, our aim was to promote osteogenic differentiation of human adipose stem cells (hASCs) encapsulated in gellan gum (GG) or collagen type I (COL) hydrogels with bioactive glass (experimental glass 2-06 of composition [wt-%]: Na2O 12.1, K2O 14.0, CaO 19.8, P2O5 2.5, B2O3 1.6, SiO2 50.0) extract based osteogenic medium (BaG OM) for bone construct development. GG hydrogels were crosslinked with spermidine (GG-SPD) or BaG extract (GG-BaG). Methods Mechanical properties of cell-free GG-SPD, GG-BaG, and COL hydrogels were tested in osteogenic medium (OM) or BaG OM at 0, 14, and 21 d. Hydrogel embedded hASCs were cultured in OM or BaG OM fo…

SerumAdipose stem cellCompressive StrengthAdipose tissueCell Count02 engineering and technologySpectrum Analysis Raman01 natural sciencesMineralization (biology)Hydrogel Polyethylene Glycol Dimethacrylatelaw.inventionchemistry.chemical_compoundOsteogenesislawOsteogenic differentiationBioactive glassMineralsTissue ScaffoldsbiologyStem CellsPolysaccharides Bacterialbioactive glassCell DifferentiationMiddle Aged021001 nanoscience & nanotechnologyGellan gumCross-Linking ReagentsAdipose TissueMechanics of MaterialsBioactive glassSelf-healing hydrogelsOsteocalcinFemaleStem cellimplantit0210 nano-technologyMaterials scienceCell SurvivalOsteocalcinosteogenic differentiationchemistry.chemical_elementBioengineeringmacromolecular substancesCalciumta3111010402 general chemistryCollagen Type ICollagen type I hydrogelBiokemia solu- ja molekyylibiologia - Biochemistry cell and molecular biologylasiBiomaterialsCalcification Physiologicbiologinen aktiivisuusgellan gum hydrogelAnimalsHumansta217Ionsgeelitta1182adipose stem cellkantasolutRats0104 chemical sciencesDurapatiteGene Expression RegulationchemistryBiophysicsbiology.proteinGlassGellan gum hydrogelluukudoksetcollagen type I hydrogelBiomarkersMaterials Science and Engineering: C
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A Multi-Component Reaction towards the Development of Highly Modular Hydrogelators

2018

Herein we report a multi‐component reaction approach for the development of a new class of hydrogelators based on the OxoTriphenylHexanOate (OTHO) backbone. A focused library of OTHOs has been synthesized and their hydrogelation features evaluated. The two most potent hydrogelators were studied by rheology revealing different stiffness, appearances and thixotropic behavior of the gels. The new gelators showcase the versatility of the OTHO backbone as a platform for the design of functionalized hydrogels with tunable gel properties. peerReviewed

Thixotropymulticomponent reactionNanotechnologypi interactions010402 general chemistry01 natural sciencesCatalysispyridine N-oxideRheologyMulti-component reactionta116geelitkemiallinen synteesi010405 organic chemistryChemistrybusiness.industryOrganic ChemistryGeneral Chemistryself-assemblyModular designgels0104 chemical sciencesSelf-healing hydrogelsSelf-assemblybusiness
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Triggering a transient organo-gelation system in a chemically active solvent

2021

A transient organo-gelation system with spatiotemporal dynamic properties is described. Here, the solvent actively controls a complex set of equilibria that underpin the dynamic assembly event. The observed metastability is due to the in situ formation of a secondary solvent, acting as an antagonist against the primary solvent of the organogel. peerReviewed

geelitPhysics::Biological PhysicsQuantitative Biology::BiomoleculesChemistryEvent (relativity)Metals and AlloysGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSolventliukeneminenCondensed Matter::Soft Condensed MatterChemical physicstermodynamiikkaMetastabilityMaterials ChemistryCeramics and CompositesTransient (oscillation)Physics::Chemical Physicsorgaaniset yhdisteet
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