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  • Electronic Resource  (6)
  • Polymer and Materials Science  (5)
  • angiotensin II receptors  (1)
  • 1
    ISSN: 1432-1041
    Keywords: angiotensin II analogues ; angiotensin II receptors ; 1-sarcosine ; 8-threonine angiotensin II ; 1-sarcosine ; 8-isoleucine angiotensin II ; 1-sarcosine ; 8-alanine angiotensin II ; blood pressure ; plasma aldosterone concentration ; plasma renin activity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The biological effects of 1-Sarcosine, 8-Threonine angiotensin II ([Sar1, Thr8]ANG II) on blood pressure, plasma aldosterone concentration (PAC) and plasma renin activity (PRA) were investigated in six normal subjects on an unrestricted diet, and compared with those of 1-Sarcosine, 8-Isoleucine ANG II ([Sar1, Ile8]ANG II) and 1-Sarcosine, 8-Alanine ANG II ([Sar1, Ala8]ANG II). All three ANG II analogues (A II A) showed agonistic pressor activity, that of [Sar1, Ile8]ANG II being greater than that of [Sar1, Thr8]ANG II or [Sar1, Ala8]ANG II. The antagonistic effect of [Sar1, Thr8]ANG II on blood pressure was less than [Sar1, Ile8]ANG II or [Sar1, Ala8]ANG II. Both [Sar1, Ile8]ANG II and [Sar1, Ala8]ANG II increased PAC and blocked the steroidogenic action of ANG II, while [Sar1, Thr8]ANG II showed little effect on PAC. All three A II A caused similar suppression of PRA and showed no inhibitory effect on the decrease in PRA produced by ANG II. These results indicate that [Sar1, Thr8] ANG II is an A II A with weak agonistic pressor action and that it has vascular selective properties. It is also suggested that ANG II receptors in a variety of target organs are heterogeneous.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 24 (1986), S. 325-335 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phase separation temperatures of the ternary system polystyrene (PS) (Mw = 1.67 × 104)/poly(α-methyl styrene) (PαMS) (Mw = 9.0 × 104)/cyclopentane with a blend ratio PS/PαMS = 55/45 have been determined over the polymer concentration range 0.02 ≤ ψPS + PαMS ≤ 0.52, where ψ PS + PαMS is the segment fraction of polymer in ternary system. Phase separation temperatures for the upper critical separation in the ternary system decrease with increasing ψ PS + PαMS over the range 0.1 ≤ ψ PS + PαMS ≤ 0.52. The vapor - liquid equilibrium in this system with a blend ratio PS/PαMS=50/50 has been determined over the concentration range 0.925 ≤ ψPS + PαMS 〈 0.995 and the temperature range 60-100°C by the piezoelectric vapor sorption method. The polymer - polymer interaction parameters χ′12 determined are positive except at 100°C and increase with increasing ψ PS + PαMS. Values of χ′12 extrapolated to zero solvent concentration are positive (0.0-1.3) over the temperature range measured. Phase separation behavior is discussed in terms of phase separation temperature in a ternary system and the polymer-polymer interaction parameter.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 21 (1983), S. 2049-2056 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The segment fraction Ψ1 activity coefficients, a1/Ψ1, of solvents have been determined by the piezoelectric sorption method for 0.1 ≤ Ψ1 ≤ 0.5 in binary solutions of chlorinated methanes [carbon tetrachloride (CCl4), chloroform (CHCl3), and dichloromethane (CH2Cl2)] with aromatic hydrocarbons (benzene and toluene) in poly(methyl methacrylate), poly(methyl acrylate), poly(ethyl methacrylate), and poly(n-butyl acrylate) at 23.5°C. The present results for toluene in PMMA agree with previously published values obtained by gas-liquid chromatography. For CCl4 and the aromatic hydrocarbons, the polymer-solvent interaction parameter χ is positive and constant, while for the polar solvents (CHCl3 and CH2Cl2), χ is negative and increases with increasing Ψ1. The effect of the polymer side chains on vapor sorption in nonpolar and polar solvent systems is discussed in terms of the χ parameter.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 805-814 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vapor sorption isotherms in binary solutions of polyisobutylene (PIB), (Mη = 4.7 × 106 g/mol) in hydrocarbons (cyclopentane; cyclohexane; n-heptane; 2,2-dimethyl butane; and 2,2,4-trimethyl pentane) and chlorinated methanes [carbon tetrachloride (CCI4) and chloroform (CHCI3)] have been determined at 23.5°C using the piezoelectric sorption method. The polymer-solvent interaction parameter χ obtained agrees with previously published values determined by using gas-liquid chromatography and a quartz-helix vapor sorption apparatus. The Flory theory of corresponding-states has been applied to the experimental results through the χ parameter and affords a good prediction of the concentration dependence of χ for solutions of chloroform, carbon tetrachloride, n-heptane, and 2,2-dimethyl butane in PIB. The experimental values of \documentclass{article}\pagestyle{empty}\begin{document}$ [\partial (a_1 /\psi _1 )/\partial a_1 ]_{T,P} $\end{document} for the PIB solutions are constant over the measured concentration range, for example \documentclass{article}\pagestyle{empty}\begin{document}$ [\partial (a_1 /\psi _1 )/\partial a_1 ]_{T,P} $\end{document} = -4.1 for CCI4, -3.65 for CHCI3, -3.0 for 2,2-dimethyl butane and n-heptane, -2.7 for 2,2,4-trimethyl pentane, -2.7 for cyclohexane, and -1.7 for cyclopentane, where a1 is the solvent activity and ψ1 is the solvent segment fraction. The correlations between the values of \documentclass{article}\pagestyle{empty}\begin{document}$ [\partial (a_1 /\psi _1 )/\partial a_1 ]_{T,P} $\end{document} and the theories of Guggenheim, Miller, Huggins, and Flory are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 307-320 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Activity coefficients of benzene, toluene, cyclohexane, carbon tetrachloride, chloroform, and dichloromethane in binary solutions with polystyrene at 23.5°C have been determined using a piezo-electric sorption apparatus. The investigated solvent concentration ranges were 15 to 39 wt % for benzene, 14 to 29 wt % for toluene, 15 to 28 wt % for cyclohexane, 26 to 38 wt % for carbon tetrachloride, 24 to 46 wt % for chloroform, and 21 to 41 wt % for dichloromethane. The polystyrene (weight-averaged) molecular weights were 1.1 × 105 and 6.0 × 105 g/gmole. The weight-fraction activity coefficients (Ω1 = a1/w1) of cyclohexane, toluene, and carbon tetrachloride in polystyrene solutions determined in this work agree within experimental error with previously published values determined by measurement of vapor pressure lowering and vapor absorption by thin films. We find disagreement, at low solvent concentrations, between our results for benzene and chloroform and previously published results. We have analyzed our results using Flory's version of corresponding-states polymer solution theory. The theory can account, qualitatively, for the cyclohexane and carbon tetrachloride results. It cannot account for the toluene, benzene, dichloromethane, or chloroform results.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 793-803 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Vapor-liquid equilibria in binary solutions of hydrocarbons (n-hexane, benzene, toluene, cyclohexane) and chlorinated methanes [carbon tetrachloride (CCl4), chloroform (CHCl3), and dichloromethane (CH2Cl2)] in polybutadiene (PBD) and polyisoprene have been determined at 23.5°C by using the piezoelectric sorption method. The weight-fraction activity coefficient of solvent (a1/w1) in cis-PBD (98% cis-1,4 addition) and random cis-trans-PBD (r-PBD, 34.3% cis-1,4 addition; 54.3% trans-1,4 addition; 11.4% vinyl-1,2 addition) are almost equal for CCI4, CHCI3, CH2CI2, benzene, and toluene solutions, while the values of a1/w1 in n-hexane and cyclohexane solutions in cis-PBD are larger than those in r-PBD solutions. The values of a1/w1 for solutions of hydrocarbons and chlorinated methanes in cis-1,4 polyisoprene (95% cis-1,4 addition) have been compared with those for cis-PBD.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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