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  • Gas chromatography-mass spectrometry  (4)
  • Mechanical simulation  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 24 (1986), S. 150-156 
    ISSN: 1741-0444
    Keywords: Finite element model ; Left ventricle mechanics ; Mechanical simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract The model of the left ventricle (LV) mechanics presented in Part 1 of the paper is used to simulate an entire cardiac cycle. Time-sequential canine heart data obtained by dynamic computerised tomography serve to initiate the simulation as well as to provide real data for evaluation of its results. The numerical predictions of the dynamic geometric changes are in good agreement with the tomographically determined changes that the ventricle undergoes throughout the cycle. Moreover, the simulation allows the evaluation of the time-varying stress and strain distributions in the ventricular wall and the active forces prevailing in the myocardial fibres. The simulated shape of the LV during the entire cardiac cycle reasonably compares with the experimental data. Furthermore, the twist angle of the ventricle as well as its maximal mean fibre strain are found to be in good agreement with physiological findings. Finally, a parametric study gives the relative influence of the anisotropy of the myocardium, its geometric and material nonlinearities and the mechanical activation on the mechanics of the left ventricle.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 24 (1986), S. 145-149 
    ISSN: 1741-0444
    Keywords: Finite-element model ; Left ventricle mechanics ; Mechanical simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract A comprehensive numerical model, based on the finite-element method, for the continuous simulation of the complete cardiac cycle is presented. The model uses real, measuredin vivo, three-dimensional geometry of the ventricle, and accounts for the anisotropy of the ventricular wall, the large deformations it undergoes during the cardiac cycle, the material nonlinearity of the myocardium and its mechanical activation. The simulation process is carried out incrementally while adjusting the mechanical activation for each increment so as to produce the same change in cavity volume as that measured experimentally. A detailed analysis of a complete cycle of the canine heart is presented in Part 2 of the paper.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 25 (1987), S. 284-288 
    ISSN: 1741-0444
    Keywords: Finite-element model ; Infarction ; Ischaemia ; Left ventricle mechanics ; Mechanical simulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Several ischaemic states, including immediate infarction, occurring in a canine left ventricle at the onset of the ejection phase and affecting regions of varying sizes are simulated, employing a recently developed comprehensive finite-element model. The analysis assumes an instantaneous partial or complete loss of contractility in the damaged region, whereas the passive mechanical properties of the tissue are yet unaltered. The results indicate a progressive deterioration of the cardiac performance, as well as considerable geometrical changes in the kinematics of the whole ventricle, directly related to both ischaemia level and the ischaemic region size. Owing to the reduction in the stroke volume, the simulation predicts a degradation of up to 33 per cent in the ejection fraction for an infarct affecting 43 per cent of the ventricular wall volume. A quantitative relationship between the ejection fraction, the level of ischaemia and the size of the ischaemic zone is derived and presented.
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  • 4
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Shikimic, quinic, chlorogenic acids ; o-Phosphoric acid ; 5-Hydroxymethylfufurol ; Model solution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Fragmentation patterns and quantitation possibilities of gas chromatography-mass spectrometry (GC-MS) with Ion Trap Detection (ITD) are reported for the trimethylsilyl (TMS) derivatives of selected aliphatic and aromatic/cyclohexanoic, mono-, di- and polyhydroxy/methoxy carboxylic acids,o-phosphoric acid, proline and 5-hydroxymethylfurfurol (HMF)— (common in natural matrices, such as fruits, honey etc.). In order to maintain stability of derivatives, their stock solutions were diluted with hexamethyldisilazane. Quantitation was carried out simultaneously on the basis both of the total ion current (TIC) and selective fragment ion (SFI) values. Data obtained proved that (i) the fragmentation of different TMS acids provided very informative, utilizable characteristics, that were also suitable for quantitation; (ii) the type of fragments do not differ in their m/z values compared to those obtained in the Mass Spectral Database; (iii) the advantages of ITD due to its ‘soft’ fragmentation feature resulted in higher abundance of characteristic ions $$[M]^{_ \cdot ^ + }$$ , ([M−CH3]+, [M+1]+, [M+TMS]+, [M+2TMS]+) compared to the non characteristic reagent ones (at m/z=73,147). Determination of oxalic, glycolic, pyruvic, levulinic, succinic, malic, pimelic, tartaric, citric, palmitic, oleic, stearic, arachidic, shikimic, quinic, chlorogenic acids, as well as those ofo-phosphoric acid, HMF and proline have been carried out in the concentration range of 1–20 ng of compounds. Reproducibility on the basis of TIC and SFI values, in the order listed, proved to be 0.8–8.6% and 1.3–16.0% (relative standard deviation percentages).
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  • 5
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Basidiomycetes ; Polysaccharides ; Hydrolysis ; Acid/sugar quantitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The simultaneous quantitation of acids and sugars as their trimethyl silyl (TMS) derivatives has been extended in order to identify and quantitate the simple acid and sugar constituents in the hydrolyzates of various immunostimulant, water-soluble polysaccharides obtained from various Basidiomycetes, such as Armillariella mellea, Auricularia auricula-judae, Coriolus versicolor, Flammulina velutipes, Fomes fomentarius, Ganoderma applanatum, Ganoderma lucidum, Pleurotus ostreatus, Schizophyllum commune, Trametes hirsuta. Optimum hydrolysis conditions, performed with 2 M trifluoroacetic acid (TFAA) for five hrs, proved the presence of several sugars and acids with maximum recovery. (i) the total sugar/sugar alcohol content of polysaccharides varied between 20- and 65% and consisted of arabitol (0.01–10.2%), arabinose (0.09–1.3%), ribose (0.2–1.8%), fucose (0.3–1.2%), mannitol (0.01–5.3%), sorbitol (0.01–0.05%), galactiol (0.04%), fructose (0.08–0.8%), galactose (0.9–29%), glucose (10–53%), uronic acids (0.14–3.7%), sucrose (0.03–2%), trehalose (0.2–1%), cellobiose (0.01–0.6%), maltose (0.2–1.9%), other disaccharides (0.2–8%). (ii) The total of acids varied from 1.5 to 30% including o-phosphoric (1.3–19%), malic (0.08–4.7%), citric (0.08–4.7%), isocitric; (3%) and C16−C18 fatty acids (1–6%).
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  • 6
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; TMS-aromatic acids ; Fragmentation patterns ; TIC/fragment ions ; Quantitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary This paper describes the fragmentation patterns and the GC-MS quantitation possibilities of the trimethylsilyl derivatives of thirty-one aromatic carboxylic acids, using ion trap detection (ITD). Sixteen aralkyl carboxylic acids, including those containing a saturated aliphatic side chain {phenylacetic, 2-phenylbutyric, phenylglycolic (mandelic acid), β-phenyllactic, 3-hydroxyphenylacetic, β-phenylpyruvic and 3-(4-hydroxyphenyl)-propionic acids} and those with an unsaturated aliphatic side chain {cinnamic, 2-hydroxycinnamic (o-coumaric), 4-methoxycinnamic, 3-hydroxycinnamic (m-coumaric), 4-hydroxycinnamic (p-coumaric), 4-hydroxy-3-methoxycinnamic (ferulic acid), 3,4-dihydroxycinnamic (caffeic), and 4-dihydroxy-3,5-dimethoxycinnamic (sinapic) acids}, as well as, the fifteen hydroxy(methoxy) benzoic acids {benzoic, 2-hydroxybenzoic (salicylic), 3-hydroxybenzoic, 4-hydroxybenzoic, 3,5-dimethoxybenzoic, 3,4-dimethoxybenzoic (veratric), 2,6-dihydroxybenzoic (γ-resorcylic), 3-methoxy-4-hydroxybenzoic (vanillic), 2,5-dihydroxybenzoic (gentisic), 2,4-dihydroxybenzoic (β-resorcylic), 3,4-dihydroxybenzoic (protocatechuic), 3,5-dihydroxybenzoic (α-resorcylic), 2,4,5-trimethoxybenzoic (asaronic), 3,5-dimethoxy-4-hydroxybenzoic (syringic) and 3,4,5-trihydroxybenzoic (gallic) acids}, provided distinct fragmentation characteristics that were very useful for their identification and simultaneously quantitation. Based on 1–20 ng amounts of acids, very informative ions of high mass with considerable intensities ([M+TMS]+, [M+1]+), $$([M]^{_ \cdot ^ + } )$$ , ([M−CH3]+) were obtained. In the case of the cinnamic acid derivatives, several odd electron fragments are formed by the loss of CO, HCHO and/or Si(CH3)4 molecules. In the case of benzoic acids the molecular ion $$([M]^{_ \cdot ^ + } )$$ proved to be abundant in three, the [M−CH3]+ ion in nine cases out of fifteen. The special MacLafferty rearrangement product ([C6H5Si(CH3)2]+) was obtained in different yields. In addition to the TIC values, at least three, and in most cases four, selective fragment ions could be utilized for quantitation. The reproducibility of the data in the concentration range of 1–20 ng acids proved to be between 1.2 and 13.0% (R.S.D.).
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  • 7
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Honeys ; Carboxylic acids ; 5-Hydroxymethylfurfurol ; Proline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A GC-MS procedure is described for the simultaneous quantitatation of the minor and major constituents of honeys, as their trimethylsilyl derivatives, from one solution, by one injection. Selected minor components (aliphatic and aromatic carboxylic acids, members of various homologous series, together with o-phosphoric acid, proline and hydroxymethylfurfurol), have been determined on the basis of their characteristic fragment ions, in the presence of extremely high excess of honeysaccharides. Selective fragmentation of these minor compounds in the ion trap detector provided possibilities for distinguishing them. The method permitted the simultaneous quantitation of o-phosphoric, malic, shikimic, citric/isocitric, quinic, margaric, oleic and stearic acids, hydroxymethylfurfurol and proline with the extremely high sugar contents of honeys (fructose, glucose, galacturonic acid, inositol, sucrose, trehalose, turanose, maltose, gentiobiose, isomaltose, raffinose, erlose, melezitose, maltotriose, panose, isomaltotriose) and allowed the fast evaluation of sugar and acid constituents of fifteen honeys from various floral and geological origin. Results revealed that (i) the minor components varied in the concentration range of 0.0001 to 0.43%, and, (ii) together with the saccharides of honeys made up the total of identified and determined constituents from 87.8% to 98.5%. Quantitative evaluation of the minor constituents was performed on the basis of their selective fragment ion values with an average reproducibility of 6.7% (RSD).
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