Gene/Protein Disease Symptom Drug Enzyme Compound
Pivot Concepts:   Target Concepts:
Query: UMLS:C0851184 (thinning)
 11,252 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Fumed silica was surface treated by hexyl (C6), octyl (C8), decyl (C10), hexadecyl (C16), and octadecyl(C18)trimethoxysilanes, and the products were evaluated from various aspects. The amounts of alkyl group introduced on silica surface were all within the range from 22 to 25 mmol/100 g. Such fumed silicas were suspended in an epoxy resin, bisphenol type A, and their rheological properties were measured. The rheological behavior of the silica suspensions was investigated as to steady-state viscosity and dynamic moduli in order to examine the effect of alkyl chain length on interactions of hydrophobic groups on the silica surface. The stronger shear thinning behavior was observed in the surface-modified fumed silica with longer alkyl groups. However, the suspensions of the nontreated fumed silica and the fumed silicas treated by C6 silane showed Newtonian behavior even at the silica concentration of 7 wt%. The dynamic moduli G' of the silica suspensions increased with increasing alkyl chain length. The interaction of hydrophobic groups on the silica surface is mainly attributed to the rheological behavior of fumed silica suspensions in the epoxy resin. Copyright 2001 Academic Press.
...
PMID:Characteristics of Alkyltrimethoxysilane-Treated Fumed Silicas and Rheological Behavior of Fumed Silica Suspensions in an Epoxy Resin. 1142 23

A new double chained surfactant, 2-octyl-dodecanoyl-6-O-ascorbic acid (8ASC10), with a L-ascorbic acid unit as the polar headgroup was synthesized for the first time. The behavior of the compound in the dry solid state has been characterized through DSC, XRD, and SAXS measurements. The surfactant forms stable viscous organogels in the presence of suitable organic solvents and also water-induced organogels upon addition of water to the organogel. These mixtures show shear-thinning properties and are birefringent. The behavior and properties of the organogels have been studied through rheology, DSC, and SAXS experiments. The organogels possess the same antioxidant properties of the original L-ascorbic acid ring and can be used to solubilize and protect valuable organic molecules.
 ...
PMID:Organogels from a vitamin C-based surfactant. 1788 Jan 25

Certain antibiotic peptides are thought to permeabilize membranes of pathogens by effects that are also observed for simple detergents, such as membrane thinning and disordering, asymmetric bilayer expansion, toroidal pore formation, and micellization. Here we test the hypothesis that such peptides act additively with detergents when applied in parallel. Additivity is defined analogously to a fractional inhibitory concentration index of unity, and the extent and mechanism of leakage is measured by the fluorescence lifetime-based vesicle leakage assay using calcein-loaded vesicles. Good additivity was found for the concerted action of magainin 2, the fungicidal lipopeptide class of surfactins from Bacillus subtilis QST713, and the detergent octyl glucoside, respectively, with the detergent C12EO8. Synergistic or superadditive action was observed for fengycins from B. subtilis, as well as the detergent CHAPS, when combined with C12EO8. The results illustrate two mechanisms of synergistic action: First, maximal leakage requires an optimum degree of heterogeneity in the system that may be achieved by mixing a graded with an all-or-none permeabilizer. (The optimal perturbation should be focused to certain defect structures, yet not to the extent that some vesicles are not affected at all.) Second, a cosurfactant may enhance the bioavailability of a poorly soluble peptide. The results are important for understanding the concerted action of membrane-permeabilizing compounds in biology as well as for optimizing formulations of such antimicrobials for medical applications or crop protection.
 ...
PMID:Additive and synergistic membrane permeabilization by antimicrobial (lipo)peptides and detergents. 2485 40

The insertion of 1-octyl-3-methylimidazolium cations (OMIM(+)) from a diluted aqueous ionic liquid (IL) solution into a model of a bacterial cell membrane is investigated. Subsequently, the mutual interactions of cations inside the membrane and their combined effect on membrane properties are derived. The ionic liquid solution and the membrane model are simulated using molecular dynamics in combination with empirical force fields. A high propensity of OMIM(+) for membrane insertion is observed, with a cation concentration at equilibrium inside the membrane 47 times larger than in the solvent. Once inserted, cations exhibit a weak effective attraction inside the membrane at a distance of 1.3 nm. At this free energy minimum, negatively charged phosphates of the phospholipids are sandwiched between two OMIM(+) to form energetically favorable OMIM(+)-phosphate-OMIM(+) types of coordination. The cation-cation association free energy is 5.9 kJ mol(-1), whereas the activation barrier for dissociation is 10.1 kJ mol(-1). Subsequently, OMIM(+) are inserted into the leaflet of the membrane bilayer that represents the extracellular side. The cations are evenly distributed with mutual cation distances according to the found optimum distance of 1.3 nm. Because of the short length of the cation alkyl chains compared to lipid fatty acids, voids are generated in the hydrophobic core of the membrane. These voids disorder the fatty acids, because they enable fatty acids to curl into these empty spaces and also cause a thinning of the membrane by 0.6 nm. Additionally, the membrane density increases at its center. The presence of OMIM(+) in the membrane facilitates the permeation of small molecules such as ammonia through the membrane, which is chosen as a model case for small polar solutes. The permeability coefficient of the membrane with respect to ammonia increases substantially by a factor of seven. This increase is caused by a reduction of the involved free energy barriers, which is effected by the cations through the thinning of the membrane and favorable interactions of the delocalized OMIM(+) charge with ammonia inside the membrane. Overall, the results indicate the antimicrobial effect of amphiphilic imidazolium-based cations that are found in various common ILs. This effect is caused by an alteration of the permeability of the bacterial membrane and other property changes.
...
PMID:How the spontaneous insertion of amphiphilic imidazolium-based cations changes biological membranes: a molecular simulation study. 2646 22

The addition of oil to an extended surfactant-water system (sodium tetrapropylene glycol (2-ethyl)octyl ether sulfate, C10PO4SO4Na) induces the elongation of spherical micelles into oil-swollen branched wormlike micelles (WLMs) near the phase inversion point of the surfactant-oil-water (SOW) system. The hydrophilic-lipophilic-difference (HLD) framework, which has been associated with surfactant curvature, was successfully used to predict the conditions under which WLMs are produced for both polar and non-polar oils. At HLD = 0, the formation of low-curvature surfactant structures including WLMs and liquid crystals are favored in water-rich systems. Micellar growth begins around HLD = -0.5, and reaches a plateau upon the formation of a branched WLM network at HLD = 0. Above the entanglement concentration, the branched WLMs exhibit Maxwell and shear thinning behavior which is suitable for the suspension of nanoparticles, among others.
 ...
PMID:Oil-induced formation of branched wormlike micelles in an alcohol propoxysulfate extended surfactant system. 3031 Sep 14