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91.
High oleic acid oil suppresses lung tumorigenesis in mice through the modulation of extracellular signal-regulated kinase cascade 总被引:2,自引:0,他引:2
Yamaki T Yano T Satoh H Endo T Matsuyama C Kumagai H Miyahara M Sakurai H Pokorny J Shin SJ Hagiwara K 《Lipids》2002,37(8):783-788
This study was undertaken to estimate the effect of dietary high oleic acid oil (OA) on 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone
(NNK)-induced lung tumorigenesis in mice. Diet containing 10% oil was fed to mice through experimental periods. On day 30
after NNK injection (100 mg/kg body weight, i.p.), the treatment increased the level of prostaglandin E2 (PGE2) as well as proliferating cell nuclear antigen, a marker of cell proliferation in a high linoleic acid oil (LA)-fed group
but not in an OA-fed group. The NNK treatment also induced the activation of an extracellular signal-regulated kinase (Erk)
cascade (Erk, Mek and Raf-1) in an LA-fed group. On the other hand, OA feeding abolished the NNK-induced activation of the
Erk cascade. In conjugation with these events, OA feeding reduced lung tumor incidence and tumor multiplicity (percentage
of mice with tumors) in mice compared with LA feeding at the 20th experimental week. These results suggest that OA suppresses
lung tumorigenesis and that this suppression is correlated with the inhibition of PGE2 production and inactivation of the Erk cascade. 相似文献
92.
Transition of the flow in a periodically grooved channel is numerically investigated for periodicity indices m=1 up to 6 by assuming the two-dimensional and fully developed flow field, where m is defined as a number of grooves in which the flow repeats periodically. Critical Reynolds numbers for the onset of a self-sustained oscillatory flow from a steady-state flow are evaluated by numerical simulations. It is found that the bifurcations occur at the critical Reynolds numbers as a result of Hopf bifurcation, and a period in the streamwise direction of the oscillatory flow is twice as long as the groove pitch of the channel. In addition, flow visualization with the aluminum dust method is carried out to confirm the results obtained from the numerical simulations. The experimental results are in good agreement with the numerical ones. 相似文献
93.
Soo‐kyung Shin Myung‐jin Jun Hyungki Hong 《Journal of the Society for Information Display》2014,22(2):122-128
In stereoscopic images, the crossing point of the viewing directions of the two eyes determines the perceived depth. Assuming that accommodation is affected by the positions of the crossing point, the effect of crossing point on minimum angle of resolution (MAR) was investigated. For 40 participants, MAR was measured by two‐alternative forced choice where Snellen optotype E of up and down directions were used as two kinds of stimuli. As the crossing point of the viewing direction of the left and right eyes moves farther from the sample display, the ability to identify the direction of letter E decreases at the optotype of the same line thickness. The change of MAR shows linear trends with respect to the optical power change that are the reciprocal of the distance from the participant to the crossing points located out of screen and on screen. 相似文献
94.
The interfacial reaction between styrene/maleic anhydride copolymer (SMA) and amine-terminated butadiene-acrylonitrile copolymer (ATBA) was observed using Fourier transform infrared (FTIR) imaging spectroscopy. The anhydride and amine reacted to form an imide. Each component was detected using a characteristic wavenumber, which was 1601 cm -1 for SMA, 2237 cm -1 for ATBA, and 1701 cm -1 for the imide. FTIR images were taken as the reaction proceeded at 150, 160, 170, and 180°C. At low temperatures (150 and 160°C), diffusion-controlled kinetics were observed since interdiffusion between the reactants did not appear in the images. On the other hand, both the diffusion front and the reaction front are observed in the images at high reaction temperatures (170 and 180°C), which indicates that the kinetics became reaction-controlled rather than diffusion-controlled. Absorbance profiles were extracted from the images and used for the calculation of the extent of reaction. The data were analyzed using the Frederickson and Milner theory based on the assumption of diffusion-controlled kinetics, and this theory fit the low reaction temperature data. 相似文献
95.
Toshihiko Tanaka Norio Hasegawa Hiroshi Shiraishi Shinji Okazaki 《Polymer Engineering and Science》1992,32(20):1545-1549
The multiple interference effect is one of the major causes of the fluctuation in critical dimension control (CD) and in mark detection for alignment. Suppressing this effect is critical for future photolithography. We propose a new photolithography technique called anti reflective coating on resist (ARCOR), which improves linewidth accuracy and overlay accuracy by suppressing multiple interference. ARCOR consists of relatively simple processes: A clear antireflective film is spun onto the resist prior to the mark detecting for alignment and exposure. The film is subsequently removed and the resist developed in the conventional way. ARCOR differs from ARC, which suppresses the reflection at the resist/substrate interface. ARCOR suppresses the reflection at the air/resist interface. ARCOR allows mark detection and exposure without light intensity-loss and multiple interference. The experiments mainly examine polysiloxane and perfluoroalkylpolyether as ARCOR materials. It is shown that linewidth accuracy can be improved from 0.3 to 0.03 μm. The signal-to-noise ratio of the alignment signal is drastically improved, and the overlay error is about half that of the conventional method. ARCOR is also effective for directly measuring the reflectivity at the resist/substrate interface, which is a key parameter of the multiple interference effect and the halation. Using ARCOR and a thin resist film, the measured ratio of reflected light to incident light indicates the reflectivity at the resist/substrate interface. Because, the probe light does not reflect off the resist surface and the intensity-loss at the resist surface is suppressed. With perfluoroalkylpolyether film, the measurement error is ~ 1.5%. 相似文献
96.
A new diimide–diacid monomer, N,N′‐bis(4‐carboxyphenyl)‐4,4′‐oxydiphthalimide (I), was prepared by azeotropic condensation of 4,4′‐oxydiphthalic anhydride (ODPA) and p‐aminobenzoic acid (p‐ABA) at a 1:2 molar ratio in a polar solvent mixed with toluene. A series of poly(amide–imide)s (PAI, IIIa–m) was synthesized from the diimide–diacid I (or I′, diacid chloride of I) and various aromatic diamines by direct polycondensation (or low temperature polycondensation) using triphenyl phosphite and pyridine as condensing agents. It was found that only IIIk–m having a meta‐structure at two terminals of the diamine could afford good quality, creasable films by solution‐casting; other PAIs III using diamine with para‐linkage at terminals were insoluble and crystalline; though IIIg–i contained the soluble group of the diamine moieties, their solvent‐cast films were brittle. In order to improve their to solubility and film quality, copoly(amide–imide)s (Co‐PAIs) based on I and mixtures of p‐ABA and aromatic diamines were synthesized. When on equimolar of p‐ABA (m = 1) was mixed, most of Co‐PAIs IV had improved solubility and high inherent viscosities in the range 0.9–1.5 dl g?1; however, their films were still brittle. With m = 3, series V was obtained, and all members exhibited high toughness. The solubility, film‐forming ability, crystallinity, and thermal properties of the resultant poly(amide–imide)s were investigated. © 2002 Society of Chemical Industry 相似文献
97.
Su‐Hsia Lin Hsiang‐Chien Kao Shih‐Hung Huang Ruey‐Shin Juang 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2002,77(2):168-174
The equilibrium and kinetics of solvent extraction of Cu2+ from aqueous solutions containing equimolar EDTA with Aliquat 336 in n‐decanol and kerosene at 298 K were investigated. The concentrations of Cu2+ (8–50 mol m?3), Cl? (5–60 mol m?3), and Aliquat 336 (20–100 mol m?3) were varied. A semi‐empirical model with three parameters was proposed to describe the equilibrium behavior, in which the non‐idealities in both aqueous and organic phases were considered. Over the ranges studied, the model agreed reasonably well with the experimental data (standard deviation, 15%). The forward and backward reaction rate constants were determined as (5.31 ± 0.16)×10?6 m9/4 mol?3/4 s?1 and (2.62 ± 0.09)×10?7 s?1, respectively, at 298 K. An interfacial reaction mechanism was proposed, which revealed that the reaction between the chelated anions and trimeric amine molecules at the interface was rate limiting. The derived rate laws were consistent with the experimental results. © 2002 Society of Chemical Industry 相似文献
98.
Interaction of impact shock waves that could detonate an explosive (Composition B) confined in a thin-walled container impacted by a cone-nosed projectile is numerically studied, based on the Forest Fire explosive reaction rate model. The normal impact on the container by a small projectile with a conical nose is considered. Depending on the cone angle of the nose part of the projectile, the zone of interaction of initiating shock waves can be remote from the central axis of the impact. The off-the-central-axis detonation is interpreted from the viewpoint of different interaction modes in the explosive container, which are reflected from the cassette wall, change their directions, and superimpose onto each other, leading to explosive detonation. 相似文献
99.
Liquid-phase catalytic degradation of waste polyolefinic polymers (HDPE, LDPE, PP) over spent fluid catalytic cracking (FCC)
catalyst was carried out at atmospheric pressure with a stirred semi-batch operation. The effect of experimental variables,
such as catalyst amount, reaction temperature, plastic types and weight ratio of mixed plastic on the yield and accumulative
amount distribution of liquid product for catalytic degradation was investigated. The initial rate of catalytic degradation
of waste HDPE was linearly increased with catalyst amount (4-12 wt%), while that was exponentially increased with reaction
temperature (350-430 ‡C). Spent FCC catalyst in the liquid-phase catalytic degradation of polymer was not deactivated fast.
The product distribution from catalytic degradation using spent FCC catalyst strongly depended on the plastic type. The catalytic
degradation of mixed plastic (HDPE: LDPE: PP: PS=3: 2: 3: 1) showed lower degradation temperature by about 20 ‡C than that
of pure HDPE. 相似文献
100.
Continuous solution copolymerization of methyl methacrylate with ethyl methacrylate or n-butyl methacrylate was carried out
in a continuous stirred tank reactor. Solvent and initiator used were toluene and benzoyl peroxide, respectively. Reaction
volume was 1.2 litters, residence time 3 hours and polymerization temperature 80°C. The copolymerization conversions were
analyzed by UV spectrophotometry and confirmed by measuring the solid weights of copolymers obtained after evaporating solvent.
The copolymerization of methyl methacrylate and alkyl methacrylates followed the second order kinetics. The simulated conversions
and copolymerization rates were compared with the experimental results. The average time to reach dynamic steady-state was
three and half times of the residence time. 相似文献