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  • 1
    ISSN: 1436-2813
    Keywords: P-glycoprotein ; multidrug resistance ; lung cancer ; immunohistochemistry ; postoperative chemotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The expression of P-glycoprotein in 159 non-small cell lung cancers was immunohistochemically examined using a monoclonal antibody (MoAb C219). A total of 93 (60%) cancers were found to be positive for P-glycoprotein. The 5-year survival rates of patients with P-glycoprotein (P-gp+) and those without P-glycoprotein (P-gp−) were 47.6% and 73.6%, respectively (P〈0.05). According to a univariate analysis, P-gp+ was associated with a poor prognosis for males, those with stage I cancer, those who underwent complete resection, and those with adenocarcinoma or squamous cell carcinoma. A multivariate study using the Cox regression analysis indicated that the expression of P-glycoprotein is useful for predicting the prognosis. Among 24 patients who underwent complete resection and postoperative adjuvant chemotherapy, 18 were P-gp+ and the remaining 6 were P-gp−. Of the 18 with P-gp+ cancer, 11 relapsed and 9 died from tumor-related causes, while the other 7 remain free from tumor recurrence; however, all with P-gp− cancer are alive without recurrence. These observations suggest a bias toward a shorter survival for patients with P-gp+ cancer because P-glycoprotein may be associated with chemoresistance. Thus, detection of the expression of P-glycoprotein will aid in planning appropriate adjuvant chemotherapy for patients with non-small cell lung cancer.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1436-2813
    Keywords: Key Words: P-glycoprotein ; multidrug resistance ; lung cancer ; immunohistochemistry ; postoperative chemotherapy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Electron microscopic textures of A-B type block copolymers of styrene and isoprene cast from several solvents were investigated by means of the osmium tetroxide fixation technique. The two-phase structure, i.e., the semimicro heterogeneous structure due to the microphase separation of block segments, was observed to change systematically with the fraction of block segments and the kind of solvent. Three types of fundamental domain structure were found. With the assumption that domain structure originates from micellar structure at a critical concentration in relatively dilute solution during solvent casting, the formation of the three types of domain structure and the sizes of their elements were treated in terms of the equilibria governing the formation of micelles at the critical concentration. This analysis takes into account such thermodynamic and molecular parameters as the incompatibility between the A and B segments, the solvation of the segments, the casting temperature, the total chain length of the block copolymer, and the weight fraction composition of the block copolymer. It was concluded that the block segments are preferentially oriented along the direction perpendicular to the interface between the two phases. This particular orientation-aggregation of the block segments must make the bulk properties of the block copolymer much different from those of merely mechanical mixtures of the corresponding homopolymers, even if the same semimicro heterogeneous structures are formed in the mechanical mixtures.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Copolymers of aliphatic aldehydes containing a trimethylsilyl group were prepared at -78°C in toluene using diethylaluminum diphenylamide as an initiator. The copolymer depolymerized into monomeric aldehydes on exposure to soft X-rays. When the copolymer was used as a soft X-ray resist, almost complete development was accomplished by exposure alone. No development step was required. The soft X-ray sensitivity of poly(3-trimethylsilylpropanal-co-propanal) was 50 mJ/cm2 at the film thickness of 1.0 μm. A composite resist system consisting of a novolac resin and an aldehyde copolymer containing trimethylsilyl groups has also been developed and used as an alkaline-developable positive electron-beam and soft X-ray resist.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Domain structures of solvent-cast films of A-B-A block copolymers of styrene-isoprene-styrene were studied by electron microscopy by use of the OsO4 fixation technique. The effects of varying proportions of the two components and the casting solvent upon the domain structures were examined. It is concluded that the domain formation mechanism can be discussed like that of A-B block copolymers irrespective of sequence arrangements, as Matsuo et al. suggested, by treating A-B-A or B-A-B block copolymers as A-(1/2)B or B-(1/2)A block copolymers. The five types of fundamental domain structures - spherical domains of component A in a matrix of component B, rodlike domains of A in a matrix of B, alternating lamellae of the two components, rodlike domains of B in a matrix of A, and spherical domains of B in a matrix of A - are achieved mainly by the change of the fractional composition of the two components for a given solvent. One of the most significant features of the A-B-A block copolymers in contrast to the A-B block copolymers, i.e., that A-B-A chains can interconnect two A domains, was explored by investigating (1) the swelling behavior in a solvent that is a good one for isoprene but a nonsolvent for styrene and (2) mechanical behavior above the glass transition temperature of the styrene segments.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 31 (1991), S. 1029-1032 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Polyolefinic thermoplastic elastomer (TPE) is a two-phase material in which cured EPDM (ethylene-propylene-diene rubber) particles are densely dispersed in a PP (polypropylene) matrix. It can be melt-processed at high temperatures and behaves like a vulcanized rubber at ambient temperature. The question is on its strain recovery, i.e., why the TPE can shrink back from the highly deformed states, even though the matrix consists of the ductile polymer. We constructed a two-dimensional model with four rubber inclusions in ductile matrix and carried out the elastic-plastic analysis on the deformation mechanism of the two-phase system by FEM (finite element method). FEM analysis revealed that, even at the highly deformed states at which almost the whole matrix has been yielded by the stress concentration, the ligament matrix between rubber inclusions in the stretching direction is locally preserved within an elastic limit and it acts as an “in-situ formed adhesive” for interconnecting rubber particles. It will provide a key mechanism of the strain recovery in the two-phase system.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 33 (1993), S. 175-182 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The change in morphology and interface quantities have been analyzed for an immiscible polymer blend during reactive processing. A model polymer/polymer combination, hydroxy-terminated poly(ε-caprolactone)/liquid rubber with α, ω-carboxy groups, was employed. The blend was subjected to light scattering measurements, ellipsometry, and gel permeation chromatography (GPC). Size reduction of the dispersed phase during processing was followed by a systematic decrease in the correlation distance ζ and an increase in the specific interfacial area Ssp, both by the Debye-Bueche plot of light scattering profiles. Also observed was the time variation of the volume fraction of interface Vλ estimated as a product of the Ssp and the interfacial thickness by ellipsometry. The changes in ζ, Ssp, and Vλ with processing were accelerated when a coupling agent,γ-aminopropyltriethoxysilane (APS), was added. The amount of block copolymer formed in-situ in the APS-loaded system was estimated by GPC with RI and UV detectors. For the size reduction kinetics in both APS-loaded and -unloaded systems, Rittinger's law was found to be applicable.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 32 (1992), S. 1863-1869 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: A ternary alloy of polyamide-6 (PA), poly(phenyleneether) (PPE), and rubber has a three-phase structure, in which PPE particles with rubber inclusions are dispersed in a PA matrix. This is an excellent thermoplastic with high impact strength and high heat resistance. To understand the morphology-properties relationship, we undertook a two-dimensional finite element method (FEM) analysis on the deformation mechanism of the ternary alloy. A three-phase model was constructed so that five hybrid particles of PPE-shell and rubber-core were embedded in the PA matrix. When the model was deformed at room temperature, the rubber domain induced yielding of the PPE-shell and the PA-matrix and at large strains the yielded zone expanded to pervade the whole space. This suggests that the toughening mechanism is essentially the same as in the binary alloy of PA and rubber (rubber-toughened PA). At higher temperatures (e.g., at 100°C) the stress concentration occurred not only in the PA matrix but also in the PPE-shell. It implies that the PPE-shell is highly responsible for bulk deformation, even though it is part of the dispersed phase. At high temperatures, the rigidity of PPE affects the alloy bulk rigidity so that the ternary system exhibits high heat resistance.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: The dispersions of both reactive and nonreactive polymer-polymer blend systems achieved in three different mixers are compared. The dispersions are prepared using an industrial scale twin-screw extruder, a laboratory internal mixer, and a miniature cup and rotor mixer. The morphology development in the three mixers is remarkably similar: The dispersed phase is stretched into sheets and ribbons; these sheets and ribbons then break into cylinders, which subsequently break into droplets via Rayleigh-type instabilities. Drop size distributions can be accurately predicted if we know the size of cylinders formed in the high shear fields of the mixer. There is a significant effect of quenching time on blend morphology - i.e, to properly evaluate mixing, blends must be quenched extremely quickly (well within a minute). Otherwise, we need to consider the morphology development during the quenching time, which may not be relevant to the mixing. There is a uniform shear stress in the miniature mixer, unlike the other mixers, which have varying stress levels. It is shown that a high stress level followed by a lower stress level is required in polymer blending to achieve efficient mixing. In the high stress level, the dispersed phase is stretched into extended shapes, which undergo instabilities and break up upon entering the low stress level. In the miniature mixer, the dispersed phase sees only one stress level, and thus very extended shapes persist at the end of mixing. The final dispersions in the twinscrew extruder and internal mixer at matched maximum shear rates are almost identical. For similar shear rates in the miniature mixer, the final dispersion of reactive blends is comparable to the other mixers. However, the miniature mixer does a poor job in dispersing high viscosity uncompatibilized blends, and the mixing conditions must be altered to obtain efficient mixing.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 1541-1546 
    ISSN: 0887-6266
    Keywords: blends, miscible, local order in ; light scattering, depolarized, by miscible blends of dissimilar polymers ; ordering and specific interaction in miscible blends of dissimilar polymers ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Depolarized light scattering measurements on single-phase mixtures of dissimilar polymers, poly(methyl methacrylate) (PMMA)/poly (acrylonitrile-co-styrene) (SAN, AN content = 15 wt %) and PMMA/poly (vinylidene fluoride) (PVDF) were carried out. The effective mean-square optical anisotropy γ2 of the mixtures was found to be much higher than that estimated by the simple additivity of γ2 of component polymers. From the deviation, the order parameter (1 + J12) was estimated to be in a range of 2-13, depending on the blend composition. This suggests local ordering in the single-phase mixtures, i.e., nematic alignment of the locally stretched dissimilar chains. In contrast, the deviation was slight in the polymer/solvent systems, SAN/MMA (monomer) and PVDF/butanone. The degree of ordering decreased with increasing temperature. T. The Specific interaction evidenced by FTIR spectroscopy exhibited a similar temperature dependence. Thus, local ordering seems to be induced by specific interactions and chain connectivity. The temperature dependence of J12 was successfully described by the Landau-de Gennes theory; J-112 ∞ (T + T0)/ T, T0 being the isotropic-nematic transition temperature, as in the case of liquid crystals.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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