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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Urological research 10 (1982), S. 135-140 
    ISSN: 1434-0879
    Keywords: Peyronie's Disease ; Clostrideal collagenase ; Connective tissue ; Collagen ; Injection therapy ; Scar dissolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This pilot study was designed to test the feasibility of using purified clostridial collagenase in the clinical management of Peyronie's disease. The basic properties of this agent are discussed. We studied its effect on Peyronie's plaque tissue by a quantitative in vitro assay utilising the liberation of free α-amino groups as an index of enzymatic collagenolysis. Tissue from three patients with Peyronie's disease was used. Tunica albuginea from a second group of three normal patients was studied in the same manner, and no selectivity for the collagen of Peyronie's plaques was identified. Utilising human pericardium as a uniform collagenous substrate, a simple dose-effect relationship was established, and the distribution characteristics of injected collagenase observed. Its effects on blood vessels and nerves in vivo was determined as well as the effects of collagenase on the histology of normal and diseased human tissue in vitro. A tentative dose for use in Peyronie's disease was established, which is discussed in light of existing toxicological data. The study was designed to test the eeasibility of purified collagenase in the clinical management of Peyronie's disease. Data included detail plaque digestion and dose-effect relationships in vitro, as well as the histological effects on plaques, blood vessels, and nerves in vivo and in vitro. It is concluded that collagenase may warrant further clinical testing in the treatment of Peyronie's disease.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-2568
    Keywords: GALLBLADDER MUCOSA ; MUCOSAL FLUID ABSORPTION ; LIPID ABSORPTION ; CHOLESTEROL GALLSTONES ; OBESITY
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Gallbladder mucosal absorption of fluid duringfasting is a well-known process. Indirect in vivo andrecent in vitro evidence for physiologically relevantgallbladder absorption of cholesterol and phospholipids from bile has been observed in humans. Thepresent study explored and compared by indirect meansthe relative efficiences of human gallbladder mucosalabsorption of fluid and lipids in health and disease. Biliary lipids and pigment content weremeasured in fasting gallbladder bile samples obtainedfrom gallstone-free controls and from four study groups:multiple and solitary cholesterol gallstone patients, and morbidly obese subjects with and withoutgallstones. Bile salts and pigment content weresignificantly greater in gallstone-free controls than inall other disease study groups. This was interpreted as evidence of more effective gallbladdermucosal fluid absorption in nonobese gallstone-freecontrols compared to that in all other groups.Correlation plot analyses of biliary lipids showed lowerconcentrations of phospholipids than expected from the indexbile salt concentrations. The same was found forcholesterol concentrations but only in supersaturatedsamples. These findings were much more pronounced in gallstone free-controls and were accordinglyinterpreted as evidence of more efficient gallbladderabsorption of both phospholipids and cholesterol incontrols compared with that found in each of the disease study groups. Moreover, impaired gallbladdermucosal function, while invariably associated withcholesterol gallstone disease, was not found to be anecessary consequence of the physical presence ofstones. It is concluded that efficient gallbladdermucosal absorption of both fluid and apolar lipids frombile is a normal physiological process that is oftenseriously impaired in the presence of either cholesterol gallstone disease or at least one of itsprecursor forms.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 669-677 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title reaction has been investigated in the temperature range of 490-573 K. Initial reactant pressures were varied in the range of 0.2-5.2 torr (I2) and 2-20 torr (C6H5SiH3). The rate of iodine consumption, monitored spectrophotometrically, was found to obey \documentclass{article}\pagestyle{empty}\begin{document}$$ - \frac{{d[{\rm I}_{\rm 2}]}}{{dt}} = \frac{{k_{3/2} [{\rm I}_{\rm 2}]^{{\raise0.7ex\hbox{$1$} \!\mathord{\left/ {\vphantom {1 2}}\right.\kern-\nulldelimiterspace} \!\lower0.7ex\hbox{$2$}}} [{\rm C}_{\rm 6} {\rm H}_{\rm 5} {\rm SiH}_{\rm 3}]}}{{1 + k'[HI]/[I_2]}}$$\end{document} both by initial rate and integrated equation fitting procedures. The effect of added initial HI conformed to this expression. The data are consistent with a conventional I-atom propagated chain reaction, and for the step \documentclass{article}\pagestyle{empty}\begin{document}$${\rm I}^{\rm .} + {\rm C}_{\rm 6} {\rm H}_{\rm 5} {\rm SiH}_{\rm 3} \to {\rm C}_{\rm 6} {\rm H}_{\rm 5} \mathop {\rm S}\limits^{\rm .} {\rm iH}_{\rm 2} + {\rm HI}$$\end{document} the rate constant is given by \documentclass{article}\pagestyle{empty}\begin{document}$${\rm log}k_1 (dm^3 /mol \cdot s) = (11.52 \pm 0.08) - (76.8 \pm 0.8{\rm kJ/mol})/RT{\rm ln}10$$\end{document} From this is derived the bond dissociation energy value C6H5SiH2—H = 374 kJ/mol(88 kcal/mol). A comparison with other Si—H dissociation energy values indicates that the “silabenzyl” stabilization energy is small, ≈7 kJ/mol.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 14 (1982), S. 933-944 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The literature results for the pyrolysis of bis trifluoromethyl peroxide are reexamined and compared with those for dimethyl peroxide. The thermochemistry yields the result that the π-bond energy in carbonyl fluoride is 96 ± 10 kcal/mol compared to 74 kcal/mol for that in formaldehyde. Thermodynamic additivity contributions are derived for the C—(F)3(O) and O—(C)(F) groups. Some conclusions are drawn in relation to the oxidation of halogeno methyl radicals and the chemistry of the atmosphere.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 24 (1992), S. 127-143 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reactions of dimethylsilylene, SiMe2, generated by laser flash photolysis from pentamethyldisilane and octamethyltrisilane, and detected via its 457.9 nm absorption, have been investigated with a number of oxygen containing molecules, including oxygen itself, carbon monoxide, water, alcohols, and ethers at 295 K. Some substrate molecules were deuterated. Apart from CO, all molecules reacted with SiMe2 with second order rate constants (in cm3 molecule-1 s-1) in the range 7.7 ± 10-14 to 4.7 ± 10-11.While most of the reactions of SiMe2 studied went to completion those with dimethylether and tetrahydrofuran were partially reversible. The reaction of SiMe2 with oxirane was pressure dependent.The data are generally consistent with a mechanism involving initial formation of a donoracceptor, zwitterionic complex. In the case of reaction with alcohols, there is a small overall isotope effect, suggesting formation of a complex followed by rapid H-transfer, which only marginally affects the rate. In the case of ethers, complexes are formed which (i) may react further (Me2Si…oxetane), (ii) may react further but also reversibly decompose (Me2Si…oxirane), or (iii) do not seem to react further (Me2Si…OMe2, Me2Si…THF) but partially redissociate. The donor-acceptor bond strength has been estimated in these last cases to be ca. 40 kJ mol-1. Supporting arguments and mechanistic details of all reactions investigated are presented.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 16 (1984), S. 117-124 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The static vessel pyrolysis of bicyclo[2.2.2]octa-2,5,7-triene (barrelene) has been studied between 483 and 523 K. The products were acetylene and benzene (in equal quantities) with no other detectable C8H8 isomer (down to less than 1% of total). The time dependence fitted first-order kinetics, and the data are consistent with a homogeneous unimolecular reaction close to, if not at, its high-pressure limit at 0.25 torr. The rate constant was fitted to the Arrhenius equation \documentclass{article}\pagestyle{empty}\begin{document}$$ \log \left( {{k \mathord{\left/ {\vphantom {k {s^{ - 1} }}} \right. \kern-\nulldelimiterspace} {s^{ - 1} }}} \right)\, = \,\left( {14.27\, \pm \,0.18} \right)\, - \,{{\left( {41.71\, \pm \,0.41\,{{{\rm kcal}} \mathord{\left/ {\vphantom {{{\rm kcal}} {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}} \right)} \mathord{\left/ {\vphantom {{\left( {41.71\, \pm \,0.41\,{{{\rm kcal}} \mathord{\left/ {\vphantom {{{\rm kcal}} {{\rm mol}}}} \right. \kern-\nulldelimiterspace} {{\rm mol}}}} \right)} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}\,\ln \,10 $$\end{document} These Arrhenius parameters are shown to imply a concerted single-step process. Alternative mechanisms are discussed and a comparison is made with the retro-Diels - Alder reactions of other bicyclo[2.2.2]octa-olefin systems.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 15 (1983), S. 605-607 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Earlier arguments concerning D(CF3O2-CF3) and D(CF3-O2) are shown to be probably wrong. New values of 86 and 49 kcal/mol, respectively, are derived. C-O bond strengths are compared between CF3- and CH3-containing compounds.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Time-resolved studies of silylene, SiH2, generated by laser-flash photolysis of phenylsilane, have been employed to obtain rate constants for its bimolecular reactions with C2H2 and C2D2. The reactions have been studied in the gas-phase, in the pressure range 1-100 torr (with SF6 bath gas) at five temperatures in the range 291-613 K.Reaction with C2H2 is pressure dependent, consistent with a third body assisted association reaction. However the lack of a simple fit to RRKM calculated values suggests a more complex process with another reaction channel. Reaction with C2D2 is faster than with C2H2, showing a pressure dependent isotope effect. The data are consistent with a rapid isotopic scrambling mechanism. Further RRKM modeling of a three-channel decomposition mechanism for the suggested silirene adduct (intermediate) provides a semi-quantitative fit to the data. Rate constants extracted from the modeling are shown to be consistent with a mechanism leading to formation of both ethynylsilane and vinylsilylene, as previously proposed by O'Neal, Ring et al. from higher temperature studies. An enthalpy surface is shown to be consistent with this mechanism. © 1994 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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