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  • 1990-1994  (2)
  • 42.50.Lc  (1)
  • Nicergoline  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Applied physics 55 (1992), S. 233-241 
    ISSN: 1432-0649
    Keywords: 42.50.Dv ; 42.50.Lc ; 42.65.Ky
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract Broadband high level squeezing was clearly observed from 100 kHz to 80 MHz using crystals Ba2NaNb5O15 of 5 mm length, MgO:LiNbO3 of 19 mm length and KNbO3 of 5.8 mm length. Maximum noise reductions detected on a spectrum analyzer were −1.2 dB (−24%), −1.25 dB (−25%), and −1.8 dB (−34%) for the three crystals, respectively. The maximum squeezing is limited mostly by “optical index damage” of the parametric crystals. A detailed analysis of the beam parameters traced along the pump beam, squeezed vacuum, etc. is given. A detailed discussion on the evaluation of the initial squeezed level is given. A preliminary experiment with compressed laser pulses to avoid the optical damage is also described.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 32 (1991), S. 179-181 
    ISSN: 1612-1112
    Keywords: Thin-layer chromatography ; Secondary ion mass spectrometry ; Nicergoline ; Semisynthetic alkaloid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A direct combination of thin-layer chromatography with secondary ion mass spectrometry (TLC/SIMS) provides a method for the quantitative analysis of thermally unstable compounds or compounds of low volatility such as nicergoline. The method is very simple and has excellent precision. The analysis was performed by using an aluminium TLC plate and a mixture of methylene chloride, acetone, and distilled water as a developing solvent. After development the portion of the plate with the nicergoline and the internal standard spots was cut off the TLC plate, and was attached to the SIMS holder directly. The amount of nicergoline was determined from the ratio of the fragment ion intensity of the nicergoline to the internal standard. The calibration curve was linear, and the detection limit was 10 ng at a signal-to-noise ratio of 5. This method should be considered for application to the determination of drugs in biological samples and also for the determination of possible impurities and decomposition products in drugs.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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