Search results for "ionic"

showing 10 items of 2016 documents

Multifunctional Cationic PeptoStars as siRNA Carrier: Influence of Architecture and Histidine Modification on Knockdown Potential.

2019

RNA interference provides enormous potential for the treatment of several diseases, including cancer. Nevertheless, successful therapies based on siRNA require overcoming various challenges, such as poor pharmacokinetic characteristics of the small RNA molecule and inefficient cytosolic accumulation. In this respect, the development of functional siRNA carrier systems is a major task in biomedical research. To provide such a desired system, the synthesis of 3-arm and 6-arm PeptoStars is aimed for. The different branched polypept(o)idic architectures share a stealth-like polysarcosine corona for efficient shielding and a multifunctional polylysine core, which can be independently varied in s…

Small RNAGene knockdownDrug CarriersPolymers and PlasticsChemistryCationic polymerizationBioengineering02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesIn vitro0104 chemical sciencesBiomaterialschemistry.chemical_compoundCytosolRNA interferencePolylysineMaterials ChemistryBiophysicsHistidineRNA Small Interfering0210 nano-technologyHistidineBiotechnologyMacromolecular bioscience
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Enhancing Gene Knockdown Efficiencies by Comparing siRNA-Loaded Cationic Nanogel Particles of Different Sizes

2015

lt;pgt;In order to silence the expression levels of pathogenic genes, small interfering RNA (siRNA) requires a nano-sized carrier for its safe and stable delivery into cells. In this research highlight, we focus on well-defined cationic nanohydrogel particles developed in our group for such purposes. To investigate the nanogels’ mechanism for enhanced knockdown efficiencies, we recently synthesized two sets of particles with similar material composition and siRNA-loading characteristics, but – according to the manufacturing process – of different sizes. Within this study, 100-nm-sized nanogel particles loaded with siRNA accumulated inside the lysosomes already after 4 h and could not induce…

Small interfering RNAGene knockdownRNA interferenceCationic polymerizationBiophysicsDistribution (pharmacology)Translation (biology)General MedicineBiologyMolecular biologyIntracellularNanogelRNA & DISEASE
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Ion-exchange fibers and drugs: an equilibrium study

2001

The purpose of this study was to investigate the mechanisms of drug binding into and drug release from cation-exchange fibers in vitro under equilibrium conditions. Ion-exchange groups of the fibers were weakly drug binding carboxylic acid groups (-COOH), strongly drug binding sulphonic acid groups (-SO(3)H), or combinations thereof. Parameters determining the drug absorption and drug release properties of the fibers were: (i) the lipophilicity of the drug (tacrine and propranolol are lipophilic compounds, nadolol is a relatively hydrophilic molecule), (ii) the ion-exchange capacity of the fibers, which was increased by activating the cation-exchange groups with NaOH, (iii) the ionic streng…

SodiumCarboxylic acidPharmaceutical Sciencechemistry.chemical_element02 engineering and technology030226 pharmacology & pharmacyDivalent03 medical and health sciencesDrug Delivery Systems0302 clinical medicineFiberchemistry.chemical_classificationChromatographyOsmolar Concentration021001 nanoscience & nanotechnologyPropranololIon ExchangeNadololSolubilitychemistryIonic strengthLipophilicityTacrineCalcium0210 nano-technologyDrug carrierDrug metabolismNuclear chemistry
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LC of high to moderately polar basic drugs in urine with water and detergent, and direct injection

2016

Background: Micellar LC was first proposed as a ‘green’ mode using mobile phases of water and surfactant. However, in most procedures a small amount of organic solvent is required to decrease the retention to convenient values. Results & methodology: Mixed micellar mobile phases prepared with both cationic (sodium dodecyl sulphate) and nonionic surfactant (Brij-35) modulate the retention of high to moderately polar basic drugs to practical times, eliminating the need of organic solvent. While the mobile phase is continuously recycled through the system, the stationary phase performance is maintained after repetitive injection of the samples. Discussion & conclusion: Through an exte…

SodiumClinical Biochemistrychemistry.chemical_elementUrine010402 general chemistry01 natural sciencesPolyethylene GlycolsAnalytical ChemistrySurface-Active AgentsPulmonary surfactantLimit of DetectionPhase (matter)HumansGeneral Pharmacology Toxicology and PharmaceuticsMicellesChromatographyChemistryOrganic solvent010401 analytical chemistryCationic polymerizationSodium Dodecyl SulfateWaterGeneral Medicine0104 chemical sciencesMedical Laboratory TechnologyPharmaceutical PreparationsStationary phaseFlow Injection AnalysisPolarChromatography LiquidBioanalysis
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Retention of vanadium (V) by three Finnish mineral soils

1994

Summary Retention of V(V) by three Finnish mineral soils from 10−4m and 10−5m sodium vanadate solutions was investigated at room temperature in the pH range 2.3–7.5. In adsorption experiments, 0.02 m KCl was used as ionic medium, and the samples were left to equilibrate for 72 h. The solid: solution ration was 1:100 (m: v). Maximum adsorption occurred at pH ∼4, where 70–80% of the added V (350–400 μg g−1 from 10−4m solution and 35–40 μg g−1 from 10−5m solution) was retained by each soil. Retention was significant even at pH 6, where adsorption of a similar anion, molybdate, is negligible. Desorption of the retained V was measured by adding 50.0 cm3 of 0.02 M KCl into weighed soil samples an…

Soil testChemistryInorganic chemistrySoil ScienceIonic bondingVanadiumchemistry.chemical_elementMolybdatechemistry.chemical_compoundAdsorptionDesorptionSoil waterVanadateNuclear chemistryEuropean Journal of Soil Science
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Solid state ionics and optical materials technology for energy efficiency, solar energy conversion, and environment control

1991

The fundamental electronic properties (including optical) of a solid are determined by the character of the interaction between its ionic and electronic subsystems. The state of the ionic subsystem can be changed persistently and reversibly by an external stimulus (current, light). The pertinent ion-controlled phenomena in the solids (solid electrolytes or mixed conductors) causes the ions to be inserted, extracted, transferred, or absorbed or transforms the states of the ions by redox reactions in the bulk or on the surface of the solid or on the interface of a (laminar or planar) solid ionic heterosystem. Several functions can be accomplished: (1) the optical response function of the soli…

Solid state ionicsChemical speciesMaterials sciencebusiness.industryElectrochromismFast ion conductorOptoelectronicsIonic bondingMoleculeEnergy transformationbusinessIonSPIE Proceedings
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Роль туннелирования в процессах накопления радиационных дефектов и в теории диффузионно-контролируемых реакций

1975

Advisor: Тале, Иварс

Solid state physicsCietvielu fizikaIonic crystalsPusvadītāji - defektiФизики твердого телаKristāli - defekti:NATURAL SCIENCES::Physics::Atomic and molecular physics::Molecular physics [Research Subject Categories]Щелочногалоидные кристаллыТуннельные процессыПолупроводники - радиационные дефекты
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Modeling the acid-base properties of molybdate(VI) in different ionic media, ionic strengths and temperatures, by EDH, SIT and Pitzer equations

2017

This paper reports the results of a study on the determination of the protonation constants of MoO42 −, in NaClaq, NaNO3aq, KClaq, at different ionic strengths (0 < I/mol dm− 3 ≤ 5.0 in NaClaq, 0 < I/mol dm− 3 ≤ 3.0 in NaNO3aq and KClaq) and temperatures (278.15 ≤ T/K ≤ 318.15 in NaClaq, only 298.15 K in NaNO3aq and KClaq), by potentiometric (ISE-H+ glass electrode) and spectrophotometric (UV/Vis) titrations. After a critical analysis of results and literature findings, the proposed speciation model takes into account the formation of two monomeric and four heptameric species, namely: MoO4H−, MoO4H2, (MoO4)7H86 −, (MoO4)7H95 −, (MoO4)7H104 − and (MoO4)7H113 −. Due to the complexity of…

Solid-state chemistryAtomic and Molecular Physics and OpticBase (chemistry)Thermodynamic parameterSpeciationInorganic chemistryThermodynamicsIonic bondingchemistry.chemical_elementProtonationProtonationCondensed Matter PhysicMolybdate010402 general chemistry01 natural scienceschemistry.chemical_compoundMolybdenum Protonation Thermodynamic parameters Aqueous solutions SpeciationMaterials ChemistryAqueous solutionPhysical and Theoretical ChemistrySpectroscopyMolybdenumchemistry.chemical_classificationAqueous solution010405 organic chemistryElectronic Optical and Magnetic MaterialCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialschemistryMolybdenumPitzer equationsJournal of Molecular Liquids
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ChemInform Abstract: Di- and Tricationic Organic Salts: An Overview of Their Properties and Applications

2014

During recent years growing interest has been devoted to the synthesis and applications of polycationic organic salts. Among them, di- and tricationic organic salts can be considered the natural evolution of monocationic ones. These last have given rise to the large class of ionic liquids. In the cases of di- and tricationic organic salts, the potential to change their structural features simply by varying the properties either of the charged heads or of the spacers separating them provides the opportunity to obtain materials suitable for different applications. This review article highlights recent progress in the study of the properties of di- and tricationic organic salts, as well as in …

Solvent systemLarge classchemistry.chemical_compoundChemistryIonic liquidGeneral MedicineCombinatorial chemistryIonChemInform
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Fine-Tuning of the film thickness of ultrathin multilayer films composed of consecutively alternating layers of anionic and cationic polyelectrolytes

2007

We have recently introduced a new method of creating ultrathin films [1–3] based on the electrostatic attraction between opposite charges. Consecutively, alternating adsorption of anionic and cationic polyelectrolytes leads to the formation of multilayer assemblies. Multilayer buildup is easily monitored by small angle x-ray scattering (SAXS). The total thickness of the multilayer assemblies increases linearly with the number of adsorbed layers, indicating a stepwise and regular deposition process. — Here, we report on the fine-tuning of the total film thickness by changing the ionic strength of the solvent from which the polyelectrolytes are adsorbed. When the anionic polyelectrolyte is ad…

SolventAdsorptionMaterials scienceChemical engineeringScatteringSmall-angle X-ray scatteringIonic strengthSelf-assemblyLayer (electronics)Polyelectrolyte
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