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  • 1
    In: Biopolymers, Wiley, Vol. 67, No. 2 ( 2002-01), p. 96-106
    Abstract: Near‐IR spectroscopic methods have been developed to determine the degree of hydration of human skin in vivo . Noncontact reflectance spectroscopic imaging was used to investigate the distribution of skin moisture as a function of location. A human study in a clinical setting has generated quantitative data showing the effects of a drying agent and a moisturizer on delineated regions of the forearms of eight volunteers. Two digital imaging systems equipped with liquid‐crystal tunable filters were used to collect stacks of monochromatic images at 10‐nm intervals over the 650–1050 and 960–1700 nm wavelength bands. Synthetic images generated from measurements of water absorption band areas at three different near‐IR wavelengths (970, 1200, and 1450 nm) showed obvious differences in the apparent distribution of water in the skin. Changes resulting from the skin treatments were much more evident in the long‐wavelength images than in the short‐wavelength ones. The variable sensitivity of the method at different wavelengths has been interpreted as being the result of different penetration depths of the IR light used in the reflectance studies. © 2002 John Wiley & Sons, Inc. Biopolymers (Biospectroscopy) 67: 96–106, 2002
    Type of Medium: Online Resource
    ISSN: 0006-3525 , 1097-0282
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2002
    detail.hit.zdb_id: 2159538-0
    detail.hit.zdb_id: 1480801-8
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2002
    In:  Applied Spectroscopy Vol. 56, No. 7 ( 2002-07), p. 813-819
    In: Applied Spectroscopy, SAGE Publications, Vol. 56, No. 7 ( 2002-07), p. 813-819
    Abstract: Raman spectra, measured for viable suspensions of M1 and MR1 cells, demonstrate spectral differences correlating with an increased protein and phospholipid content relative to DNA in the MR1 cells. The M1 and MR1 cell lines consist of rat fibroblast cells that have been transfected with a gene causing immortality, and the MR1 line has been further transfected with a gene causing tumor formation. The cell suspensions were prepared from monolayer cultures in the same phase of growth and remained viable throughout the experiment. The Raman data have been further examined by principal factor analysis with two approaches, (1) a constrained analysis to provide a relative contribution to the Raman data from cellular components, and (2) analysis of differences in the raw data files of the two cell lines. Utilizing the constrained principal factor analysis for the two cell lines analyzed separately provides a measure of the relative contribution of protein, lipid, DNA, RNA, and buffer to the cell Raman spectra. Factor analysis of M1 and MR1 Raman spectra analyzed together demonstrates that the two cell lines can be differentiated by Raman spectroscopy with no prior spectral processing.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2002
    detail.hit.zdb_id: 1474251-2
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 1998
    In:  Applied Spectroscopy Vol. 52, No. 10 ( 1998-10), p. 1264-1268
    In: Applied Spectroscopy, SAGE Publications, Vol. 52, No. 10 ( 1998-10), p. 1264-1268
    Abstract: The crystallinity of syndiotactic polystyrene (sPS) is studied by hyperspectral Raman line imaging. Images of a 140 × 1200 μm region of an sPS test piece containing 39 200 pixels/image were generated from spectra taken over the wavenumber interval between 300 and 875 cm −1 . The spectral region includes the moderate-intensity crystallinity-sensitive bands in the 770 800 cm −1 region, as well as other useful but weaker marker bands. Factor analysis was used to extract structure information from the set of spectra. Four non-noise factors were extracted; two were assigned to crystalline and amorphous sPS and the other two to background. Score images of the crystalline and amorphous sPS factors were used to visualize distribution of those species. The results were compared to the integrated Raman intensity image for the 773 cm −1 band of crystalline sPS.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1998
    detail.hit.zdb_id: 1474251-2
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  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  Applied Spectroscopy Vol. 57, No. 5 ( 2003-05), p. 154A-170A
    In: Applied Spectroscopy, SAGE Publications, Vol. 57, No. 5 ( 2003-05), p. 154A-170A
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 1474251-2
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  • 5
    In: Applied Spectroscopy, SAGE Publications, Vol. 47, No. 8 ( 1993-08), p. 1100-1114
    Abstract: This paper reports infrared absorption intensities of liquid methanol at 25°C between 8000 and 2 cm −1 . Measurements were made by attenuated total reflection spectroscopy by four different workers between 1984 and 1991, with the use of CIRCLE cells of two different lengths and with several different alignments of the cell in the instrument. Steps were taken to ensure that as few parameters as possible remained unchanged throughout the series of measurements, to try to reveal systematic errors. The reproducibility was better than ±2.5% in regions of significant absorption. In order to allow comparison between different methods, results of all methods were converted to real and imaginary refractive index spectra. Measurements were also made by transmission spectroscopy in regions of weak absorption, with results that agreed excellently with those from ATR. The ATR and transmission results were combined to give a spectrum between 7500 and 350 cm −1 . This spectrum agreed excellently with literature results from 350 to 2 cm −1 , and the two sets of measurements were combined to yield a spectrum from 7500 to 2 cm −1 . The imaginary refractive index was arbitrarily set to zero between 7500 and 8000 cm −1 , where it is always less than 2 × 10 −6 , in order that the real refractive index can be calculated below 8000 cm −1 by Kramers-Kronig transform. The results are reported as graphs and as tables of the real and imaginary refractive indices between 8000 and 2 cm −1 , from which all other infrared properties of liquid methanol can be calculated. The accuracy is estimated to be ±3% below 5000 cm −1 and ±10% above 5000 cm −1 for the imaginary refractive index and better than ±0.5% for the real refractive index. To obtain molecular information from the measurements, one calculates the imaginary molar polarizability spectrum, [Formula: see text] vs. [Formula: see text] , under the Lorentz local field assumption, and the area under [Formula: see text] bands is separated into contributions from different vibrations under several approximations. Much accuracy is lost in this process. The changes of the dipole moment during normal vibrations, and during OH, CH, and CO bond stretching and COH torsional motion, are presented.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1993
    detail.hit.zdb_id: 1474251-2
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 1995
    In:  Vibrational Spectroscopy Vol. 8, No. 2 ( 1995-1), p. 215-229
    In: Vibrational Spectroscopy, Elsevier BV, Vol. 8, No. 2 ( 1995-1), p. 215-229
    Type of Medium: Online Resource
    ISSN: 0924-2031
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1995
    detail.hit.zdb_id: 1500818-6
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  • 7
    Online Resource
    Online Resource
    AIP Publishing ; 1998
    In:  Review of Scientific Instruments Vol. 69, No. 10 ( 1998-10-01), p. 3645-3648
    In: Review of Scientific Instruments, AIP Publishing, Vol. 69, No. 10 ( 1998-10-01), p. 3645-3648
    Abstract: A novel four nuclear magnetic resonance (NMR)-tube holder is described for quantitative Raman and resonance Raman spectroscopy. This cell has advantages over other divided cell designs in producing high precision quantitation and eliminating off-axis errors. Raman spectra were obtained for both absorbing and nonabsorbing solutions, and the results compared to those obtained using a single tube holder. The relative Raman intensities in a 1:1 mixture of benzene and chloroform taken in the single holder were within 6% of those of the pure solvents taken with the four NMR tube holder. The resonance Raman scattering cross section of chromate was determined to be within 6% of the value obtained from a single-tube holder. All of these errors in accuracy and precision are within the errors normally associated with the quantitative measurement of Raman cross sections. These results show that the four-tube holder can be used for precise and accurate measurement of both Raman and resonance Raman scattering.
    Type of Medium: Online Resource
    ISSN: 0034-6748 , 1089-7623
    Language: English
    Publisher: AIP Publishing
    Publication Date: 1998
    detail.hit.zdb_id: 209865-9
    detail.hit.zdb_id: 1472905-2
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  • 8
    Online Resource
    Online Resource
    Elsevier BV ; 1994
    In:  Journal of Molecular Structure Vol. 324, No. 1-2 ( 1994-7), p. 157-176
    In: Journal of Molecular Structure, Elsevier BV, Vol. 324, No. 1-2 ( 1994-7), p. 157-176
    Type of Medium: Online Resource
    ISSN: 0022-2860
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1994
    detail.hit.zdb_id: 1491504-2
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 1997
    In:  Journal of Molecular Structure Vol. 413-414 ( 1997-9), p. 333-363
    In: Journal of Molecular Structure, Elsevier BV, Vol. 413-414 ( 1997-9), p. 333-363
    Type of Medium: Online Resource
    ISSN: 0022-2860
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1997
    detail.hit.zdb_id: 1491504-2
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  • 10
    In: Applied Spectroscopy, SAGE Publications, Vol. 48, No. 2 ( 1994-02), p. 176-189
    Abstract: This paper reports infrared absorption intensities of liquid methanol- d, CH 3 OD, at 25°C, between 8000 and 350 cm −1 Measurements were made by multiple attenuated total reflection spectroscopy with the use of the CIRCLE cell, and by transmission spectroscopy with a variable-path-length cell with CaF 2 windows. The results of these two methods agree excellently and were combined to yield an imaginary refractive index spectrum, k(ν˜) vs. ν˜, between 6187 and 350 cm −1 . The imaginary refractive index spectrum was arbitrarily set to zero between 6187 and 8000 cm −1 where k is always less than 2 × 10 −6 , in order that the real refractive index can be calculated below 8000 cm −1 by Kramers-Krönig transformation. The results are reported as graphs and as tables of the real and imaginary refractive indices between 8000 and 350 cm −1 , from which all other infrared properties of liquid methanol- d can be calculated. The accuracy is estimated to be ± 3% below 5900 cm −1 and ± 10% above 5900 cm −1 for the imaginary refractive index and better than ± 0.5% for the real refractive index. In order to obtain molecular information from the refractive indices, the spectrum of the imaginary polarizability multiplied by wavenumber, ν˜ vs. ν˜, was calculated under the assumption of the Lorentz local field. The area under this ν˜ spectrum was separated into the integrated intensities of different vibrations. Molecular properties were calculated from these integrated intensities—specifically, the transition moments and dipole moment derivatives of the molecules in the liquid, the latter under the harmonic approximation. The availability of the spectra of both CH 3 OH and CH 3 OD enables the integrated intensities and the molecular properties of the C-H, O-H, O-D, and C-O stretching and CH 3 deformation vibrations to be determined with confidence to a few percent. Further work with isotopic molecules is needed to improve the reliability of the integrated intensities of the C-O-H(D) in-plane bending, H-C-O-H(D) torsion, and CH 3 rocking vibrations.
    Type of Medium: Online Resource
    ISSN: 0003-7028 , 1943-3530
    RVK:
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1994
    detail.hit.zdb_id: 1474251-2
    SSG: 11
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