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  • Analytical Chemistry and Spectroscopy  (5)
  • Cholesterol synthesis  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Lipids and Lipid Metabolism 1082 (1991), S. 303-309 
    ISSN: 0005-2760
    Keywords: Cholesterol synthesis ; Hypercholesterolaemia ; LDL ; Pravastatin ; Simvastatin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Molecular Cell Research 1051 (1990), S. 138-143 
    ISSN: 0167-4889
    Keywords: (Human) ; Cholesterol synthesis ; LDL binding ; Lymphocyte proliferation
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-5233
    Keywords: Cellular cholesterol ; Cholesterol synthesis ; LDL binding ; LDL composition ; Type 2 diabetes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This study investigates compositional differences in low density lipoprotein (LDL) subfractions and their relationship to cellular cholesterol synthesis. We examined ten normocholesterolaemic (serum cholesterol 〈6.5 mM) non-diabetic subjects (group 1) and compared them with ten normocholesterolaemic (group 2) and ten hypercholesterolaemic (group 3) (serum cholesterol 〉6.5 mM) type 2 (non-insulin-dependent) diabetic patients. Serum cholesterol levels for groups 1, 2 and 3 were 5.19±0.27, 5.20±0.27 and 7.51±0.31 mM. LDL1 (density 1.006–1.028 g/l) and LDL2 (1.028–1.063 g/l) were isolated by density gradient ultracentrifugation. A significantly greater proportion of cholesterol was carried in LDL2 than LDL1 in all groups. There was a significantly lower cholesterol/protein ratio in LDL1 from the hypercholesterolaemic diabetic patients compared with controls. The LDL esterified/free cholesterol ratio was significantly greater in both LDL1 and LDL2 in the hypercholesterolaemic diabetic patients compared with the other two groups. There was a negative correlation between inhibition of cholesterol synthesis and the esterified/free cholesterol ratio of both LDL1 (r=0.56,P〈0.002) and LDL2 (r=0.63,P〈0.001). Cellular cholesterol of 41.0±0.3 μg/mg cell protein in the hypercholesterolaemic diabetic patients was also significantly higher compared with values of 30.32±2.0 and 34.1±4.2 μg/mg cell protein for the normocholesterolaemic non-diabetic and diabetic groups. In vitro LDL esterification led to a decrease in LDL receptor-mediated binding and resulted in a 40% reduction in the ability of the LDL to suppress cholesterol synthesis. The study demonstrates a relationship between the LDL esterified/free cholesterol ratio, LDL receptor binding and cellular cholesterol and may have implications for the understanding of hypercholesterolaemia in diabetes.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The bands at 2485 and 940 cm-1 observed in the Raman spectra of 2,5-dimercapto-1,3,4-thiadiazole represent the hydrogen-bonded ν(SH) stretching and δ(C-SH) in-plane bending modes, respectively. A quantitative study of the hydrogen bonding was carried out using intensity measurements of the bands assigned to the hydrogen-bonded and the free δ(C-SH) in-plane deformations at 940 and 919 cm-1, respectively, as a function of temperature. The Fourier transform (FT) Raman spectra were recorded over the temperature range 303-403 K using an environmental chamber fitted into the FT Raman sample compartment. The equilibrium constants between the free and the hydrogen-bonded molecules were determined over this temperature range and the average enthalpy for hydrogen-bond formation was obtained (ΔH° = -3.35 ± 0.2 kJ mol-1).
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 475-483 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The application of Raman spectroscopy to polymers and polymerization processes is surveyed and the advent of recent advances in instrumental techniques to polymer analysis is highlighted. Some of the problems of the more widely-used infrared spectroscopic methods, for example in microstructural analysis of polydienes and copolymers, are discussed and the advantages of the Raman spectroscopic technique are explained. The use of near-infrared excitation and Fourier-transform Raman instrumentation for process monitoring and polymer composite studies is discussed. Raman microscopic and waveguide spectroscopic studies of small samples and polymer coatings on substrates are considered. Other applications are mentioned in the areas of polymer orientation, surface-enhanced Raman scattering, conducting polymers, biopolymers and time-resolved studies.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The dissociation constants for an acetonitrile-zinc complex, (CH3CN)Zn2+, were measured in aqueous solutions containing zinc salts (40-80%, w/w) and acetonitrile by Raman spectroscopy. Quantitative measurements of the intensity of the free and complexed ν(CN) Raman bands at 2264 and 2320 cm-1, respectively, were used to determine the average enthalpy and entropy of the complex dissociation to free acetonitrile in the temperature range 293-343 K for a 70% (w/w) solution of zinc chloride (0.052 mol) in an aqueous solution containing acetonitrile (0.024 mol); δH° and δS° values of 8.4 ± 0.5 kJ mol-1, respectively, were determined.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 495-500 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The preparation and vibrational spectroscopic characterization of the hitherto unreported products of the copolymerization of 2,3-dimethylbutadiene and methyl methacrylate are presented. The polymers were prepared by free radical polymerization using α,α′-azobisisobutyronitrile as the initiator. Raman and Fourier transform infrared spectroscopic information on the 2,3-dimethylbutadiene-methyl methacrylate copolymer is presented for a range of copolymers differing in the 2,3-dimethylbutadiene to methyl methacrylate ratio. Quantitative information of the microstructure of the polymer and copolymer using the C=C stretching vibrations is provided by Raman spectroscopy. Evidence is presented for the splitting of the C=O stretching vibration, ascribed to aggregated syndiotactic and unaggregated syndio- and isotactic poly(methyl methacrylate) at 1734 and 1724 cm-1, respectively.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Journal of Raman Spectroscopy 24 (1993), S. 435-441 
    ISSN: 0377-0486
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to use a Fourier transform (FT) Raman spectrometer as a detector with a gel permeation chromatograph which was otherwise configured in the usual way for the measurement of molar mass distribution in polymers. A low-volume flow cell was constructed and the detector response tested both off-line and, in a preliminary way, in-line with the chromatograph. The particular objective was to establish whether it would be possible to measure the microstructural variation in polybutadiene with polymer molecular weight during the chromatographic process. The detector sensitivity was assessed for a range of polybutadienes with different cis-1,4-, trans-1,4- and vinyl-1,2- contents using tetrahydrofuran as solvent and eluent. Data obtained using visible Raman (488.0 nm) excitation and near-infrared (1064 nm) excitation were compared. Although it has been established that the Raman spectrometer is one of the best instruments for the evaluation of the microstructure of polybutadiene when used in a conventional way, it lacks the necessary sensitivity to provide quantitative information on polydienes which elute from a chromatograph. However, there is no reason in principle why an FT-Raman spectrometer should not be used as a concentration detector and for the simultaneous more detailed analysis of polymer composition or micro-structure during the chromatographic process, provided that the scattering intensity of the solute is high relative to the eluent. The potential advantages and the observed problems of what appears to be a novel experiment with an FT-Raman instrument are discussed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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