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A new intracellular delivery system based on an apoptotic protein‐loaded calcium carbonate (CaCO3) mineralized nanoparticle (MNP) is described. Apoptosis‐inducing cytochrome c (Cyt c) loaded CaCO3 MNPs (Cyt c MNPs) were prepared by block copolymer mediated in situ CaCO3 mineralization in the presence of Cyt c. The resulting Cyt c MNPs had a vaterite polymorph of CaCO3 with a mean hydrodynamic diameter of 360.5 nm and exhibited 60 % efficiency for Cyt c loading. The Cyt c MNPs were stable at physiological pH (pH 7.4) and effectively prohibited the release of Cyt c, whereas, at intracellular endosomal pH (pH 5.0), Cyt c release was facilitated. The MNPs enable the endosomal escape of Cyt c for effective localization of Cyt c in the cytosols of MCF‐7 cells. Flow cytometry showed that the Cyt c MNPs effectively induced apoptosis of MCF‐7 cells. These findings indicate that the CaCO3 MNPs can meet the prerequisites for delivery of cell‐impermeable therapeutic proteins for cancer therapy.  相似文献   
2.
Plants of the genus Wikstroemia are used in Chinese traditional medicine to treat inflammatory diseases, such as arthritis, bronchitis, and pneumonia. The present study was designed to determine whether Wikstroemia ganpi (Siebold and Zucc.) Maxim. offers a potential means of treating 2,4-dinitrochlorobenzene (DNCB)-induced atopic dermatitis (AD) in mice. Symptoms such as redness, edema, and keratinization in AD mice induced by DNCB were alleviated by the co-application of an ethanolic extract of W. ganpi for 2 weeks. The severity of skin barrier function damage was evaluated by measuring TEWL (transepidermal water loss). TEWLs of DNCB sensitized mouse dorsal skin were reduced by the application of a W. ganpi ethanolic extract, and skin hydration was increased. In addition, the infiltration of inflammatory cells into the dermis was significantly reduced, as were blood levels of IgE and IL-4, which play an important role in the expression of AD. The results of this experiment suggest that W. ganpi is a potential therapeutic agent for AD.  相似文献   
3.
In can-annular gas turbines, low-frequency thermoacoustic instabilities can arise from cross-talk interactions between neighboring combustors upstream of the first-stage turbine nozzles. In this experimental study, we investigate the influence of non-identical flame transfer functions (FTFs) between adjacent combustors on the development of self-excited thermoacoustic oscillations. To create different FTFs, we use five different swirl nozzles, one with high swirl (HS) and four with low swirl (LS), all with different porosities. We find that, compared with the LS FTFs, the HS FTF exhibits a smaller and flatter gain as well as a smaller phase difference. We attribute this behavior to differences in the flame structure and the stabilization mechanisms, namely an inner shear layer-stabilized diverging front in the HS case versus a detached reaction zone in the presence of a central jet with an outer swirl flow in the LS cases. Using two tunable lean-premixed combustors connected via a cross-talk section, we show that (i) symmetric FTF combinations (HS + HS or LS + LS) produce in-phase interactions, leading to push-push modes, but that (ii) asymmetric FTF combinations (HS + LS) produce out-of-phase interactions, leading to push-pull modes. Phase-resolved visualization of the asymmetric cases reveals that the inner shear layer-stabilized HS flame exhibits large angle fluctuations, whereas the aerodynamically stabilized LS flame is characterized by the periodic emergence of a bow-shaped front and an oval structure. For all the conditions tested, we find that asymmetry in the FTFs leads to either (i) a completely stable state with negligible amplitude or (ii) a mildly unstable state with an amplitude lower than that of the equivalent symmetric cases. These findings highlight the potential of using asymmetric FTFs for passive control of cross-talk-driven thermoacoustic instabilities in can-annular combustors.  相似文献   
4.
Polyamide/polyacrylonitrile thin‐film‐composite (TFC) nanofiltration (NF) membranes for the separation of oleic acid dissolved in organic solvents (methanol and acetone) were interfacially prepared by the reaction of trimesoyl chloride in an organic phase with an aqueous phase containing piperazine and m‐phenylene diamine. The interfacial reaction was confirmed by an investigation of the attenuated total reflection infrared spectrum. The surface morphology of the polyamide TFC membranes was examined with scanning electron microscopy. The hydrophilic properties of the membrane surfaces were conjectured on the basis of the ζ potential and contact angle. The effects of the monomer concentrations of the monomer blends (aliphatic and aromatic diamines) and drying times on various aspects of membrane performance, such as the solvents (water, alcohols, ketones, and hexane), permeation rates, and organic solute [poly(ethylene glycol) 200 and oleic acid] rejection rates, were investigated. All the membranes showed good solvent resistance. The polar solvent flux for water and methanol was higher than that for a nonpolar solvent (hexane). The membranes gave good rejection rates of oleic acid dissolved in methanol and acetone. The NF membranes were compared with various commercial membranes. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 2151–2163, 2002  相似文献   
5.
The copolymer gels showing gradual phase transition induced by temperature were synthesized by redox random copolymerization of N-isopropylacrylamide (NIPAAm) and acrylic acid (AAc) monomer under a constant electric current. The behavior of gradual phase transition induced by temperature was examined by measuring the thermal properties, pKa values and swelling ratio. The experimental results indicate that temperature-induced gradual phase transitions of poly(NIPAAm-co-AAc) gel are mainly driven by transport before polymerization and protonation/ionization of the AAc, caused by the electric current.  相似文献   
6.
An ionogenic main chain liquid crystalline polymer was synthesized. In contrast to previous studies the charged sites were incorporated into the flexible spacer and not into the mesogenic group. This was done through quaternization of 1,2-bis(4-pyridylethane) with a biphenyl-4,4′-nonanoxytoluenesulphonate. The polymer displayed thermotropic and lyotropic me-sophases. The thermotropic mesophase was smectic. Organic counterions such as meth-ylsulfonates and p-toluenesulfonates were found to be favorable to the development of mesophases, due to the increased solubility and lower isotropisation temperatures, when compared to bromide counterion containing polymers. Easy supercooling, dependence on thermal history, and the development of batonnet textures on cooling from the melt were also observed. © 1995 John Wiley & Sons, Inc.  相似文献   
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