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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 16 (1974), S. 1103-1112 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: β-Galactosidase has been purified from an ammonium sulfate precipitate of E. coli strain ML308 by biospecific adsorption on a column of agarose gel substituted with p-aminophenyl-β-D-thiogalactopyranoside. The system described using a 1.8 liter column has a useful processing capacity of 3.8 × 106 units of β-galactosidase per 2 hr cycle. This corresponds to about 5 g of pure enzyme. An electromechanical timing device operates a set of six solenoid valves and carries out a preset program consisting of sample application, washing, and elation operations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 15 (1973), S. 603-606 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0021-9304
    Keywords: poly(DL-lactide-ε-caprolactone) ; degradation ; foreign body reaction ; subcutaneous implant ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The aim of this study was to evaluate the degradation and foreign-body reaction of poly(DL-lactide-ε-caprolactone) (PLA85CL50) bars. This specific biomaterial is used for the construction of nerve guides, which can be used in the reconstruction of short nerve gaps. Subcutaneously implanted PLA85CL50 bars were harvested after implantation periods ranging from 3 to 12 months and evaluated for the rate of degradation and the degree of foreign-body reaction. It was observed that this copolymer degraded completely within 12 months and that no lactide or ε-caprolactone crystals were formed. Furthermore, we conclude that the foreign-body reaction of PLA85CL50 is very mild. These properties make the amorphous copolymer of DL-lactide and ε-caprolactone (50:50) suitable for the construction of nerve guides. © 1997 John Wiley & Sons, Inc. J Biomed Mater Res, 36, 337-346, 1997.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: One of the ways to reconstruct a nerve defect is to use a biodegradable nerve guide. The aim of this study was to establish a nerve guide constructed of an amorphous copolymer of lactic acid-caprolactone. A pilot study was set up to elucidate the effect of the tube dimensions on nerve regeneration. Four types of nerve guides, with internal diameters ranging from 1.12-1.23 mm and wall thicknesses ranging from 0.34-0.68, were tested for this purpose. We evaluated the biodegradation, foreign body reaction and nerve regeneration by light microscopy, after three different implantation times (1, 2, and 3 months). After 2 months, we observed that all types of nerve guides had changed from a transparent to an opaque and swollen state, and that they had lost their strength. The foreign body reaction was characterized by the presence of giant cells and fibroblasts surrounding the degrading nerve guide. From this pilot study, we conclude that nerve guide type 1, with an internal diameter of 1.23 mm and a wall thickness of 0.34 mm, can ensure nerve regeneration in the case of a 1-cm gap in the sciatic nerve of the rat. Nerve guides types 3 and 4, with relatively small lumens, show nerve compression due to a more pronounced swelling of the degrading tube. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0021-9304
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine , Technology
    Notes: The aim of this study was to evaluate short-term peripheral nerve regeneration across a 10-mm gap, using a biodegradable poly(DL,-lactide-ε-caprolacton) nerve guide, with an internal diameter of 1.5 mm and a wall thickness of 0.30 mm. To do so, we evaluated regenerating nerves using light microscopy, transmission electron microscopy and morphometric analysis after implantation of 12-mm nerve guides in the sciatic nerve of the rat. Evaluation times ranged from 3-10 weeks. Three weeks after reconstruction, myelinated nerve fibers could be observed in the distal nerve stump. Ten weeks after reconstruction, the regenerating nerves already resembled normal nerves. In conclusion, we show that poly(DL,-lactide-ε-caprolacton) nerve guides can be successfully applied in the reconstruction of severed nerves in the rat model. Furthermore, we have observed the fastest nerve regeneration described thus far, after reconstruction using a biodegradable nerve guide. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 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 5 (1973), S. 137-147 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclopropyl cyanide isomerizes in the gas phase at 660°-760°K and 2-89 torr to give mainly cis- and trans-crotonitrile and allyl cyanide, with traces of methacrylonitrile. The reactions are first order, homogeneous, and unaffected by the presence of radical-chain inhibitors. The rate constants are given by Overall: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.58 \pm 0.08) - (242.0 \pm 1.2){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} cis-Crotonitrile: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.01 \pm 0.11) - (237.6 \pm 1.4){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} trans-Crotonitrile: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.09 \pm 0.07) - (243.7 \pm 0.9){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} Allyl cyanide: \documentclass{article}\pagestyle{empty}\begin{document}$$\log _{10} k/{\rm sec}^{ - 1} = (14.59 \pm 0.13) - (252.0 \pm 1.8){\rm kJ}\,{\rm mole}^{ - 1} /2.303RT$$\end{document} where the error limits are standard deviations. On the basis of a biradical mechanism, it is deduced that the —CH—CN radical center is resonance stabilized by ca. 30 kJ mole-1. Approximate equilibrium data are given for interconversion of the 1- and 3-cyanopropenes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 329-331 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The high-pressure isotopic rate ratio kH/kD for isomerisation of cyclopropylamine and cyclopropylamine-N-d2 is 1.06 at 649-678 K, supporting a mechanism which does not involve migration of hydrogen from the amine group in the rate-determining step.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 27-35 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: At temperatures of 356-425°C and pressures of 15-60 Torr, cyclopropylamine reacts to give an equimolar mixture of ammonia and N-propylidenecyclopropylamine as the initial product. The reaction is first order, homogeneous, and unaffected by the presence of radical inhibitors, and thus proceeds by an initial rate-determining unimolecular isomerization to give a reactive intermediate, which then reacts with a further molecule of cyclopropylamine to give the observed products. Reaction in the presence of added aliphatic amines gives other imines in addition, and the nature of these indicates that the intermediate is propenylamine or its tautomer propylideneamine:
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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