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  • Articles  (4)
  • Articles: DFG German National Licenses  (4)
  • near-infrared spectrophotometry  (2)
  • toxicity  (2)
  • Springer  (4)
  • 1995-1999  (3)
  • 1990-1994  (1)
  • 1905-1909
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  • Articles  (4)
Source
  • Articles: DFG German National Licenses  (4)
Keywords
Publisher
  • Springer  (4)
Years
  • 1995-1999  (3)
  • 1990-1994  (1)
  • 1905-1909
Year
  • 1
    ISSN: 1573-904X
    Keywords: gelatin capsules ; moisture content ; near-infrared spectrophotometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-904X
    Keywords: gelatin ; crosslinking ; formaldehyde ; dissolution ; near-infrared spectrophotometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Purpose. To predict the degree of crosslinking from formaldehyde-stressed hard gelatin capsules (HGCs) using near-infrared spectrophotometry (NIR). Methods. HGCs were exposed to a 150 ppb atmosphere of formaldehyde for 2.25,4.60,9.42, 16.0 and 24.0 hours. The capsules were filled with fresh amoxicillin, placed in a 90° conical reflector cone, and scanned in a NIR spectrophotometer. Principal component regression (PCR) was employed to analyze the spectra of the intact capsules. Dissolution profiles were then obtained for each experimental group. Results. The dissolution of amoxicillin from the capsules at pH 1.2 was found to decrease with increasing time of exposure to the formaldehyde atmosphere. A set of principal components (PCs) was formed by a linear combination of the absorbance values at each wavelength scanned. A good correlation was established (r2 = 0.963) when PC values from the NIR spectra of the HGCs were regressed against percentage of amoxicillin dissolved at 45 minutes, at pH 1.2. Water content of the capsules was found to be the largest determinant in the variation between HGC spectra at each exposure time. Conclusions. NIR spectrophotometry, combined with PCR, was successful at not only predicting dissolution of HGCs exposed to formaldehyde, but also at determining which wavelengths contributed most to spectral variation of these stressed HGCs.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 134 (1991), S. 167-178 
    ISSN: 1573-5036
    Keywords: Al3+ ; aluminium ; hydroxy-aluminium ; phytotoxicity ; polynuclear aluminium ; rhizotoxicity ; roots ; toxicity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The aluminium (III) released from soil minerals to the soil solution under acid conditions may appear as hexaaquaaluminium (Al(H2O)6 3+, or Al3+ for convenience) or may react with available ligands to form additional chemical species. That one or more of these species is rhizotoxic (inhibitory to root elongation) has been known for many decades, but the identity of the toxic species remains problematical for the following reasons. 1. Several Al species coexist in solution so individual species cannot be investigated in isolation, even in artificial culture media. 2. The activities of individual species must be calculated from equilibrium data that may be uncertain. 3. The unexpected or undetected appearance of the extremely toxic triskaidekaaluminium (AlO4Al12(OH)24(H2O)12 7+ or Al13) may cause misatribution of toxicity to other species, especially to mononuclear hydroxy-Al. 4. If H+ ameliorates Al3+ toxicity, or vice versa, then mononuclear hydroxy-Al may appear to be toxic when it is not. 5. The identity and activities of the Al species contacting the cell surfaces are uncertain because of the H+ currents through the root surface and because of surface charges. This article considers the implications of these problems for good experimental designs and critically evaluates current information regarding the relative toxicities of selected Al species. It is concluded that polycationic Al (charge 〉2) is rhizotoxic as are other polyvalent cations.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Plant and soil 173 (1995), S. 329-335 
    ISSN: 1573-5036
    Keywords: calcium sulfite ; flue gas desulfurization residue ; oxidation ; sulfur dioxide ; toxicity ; Triticum aestivum L.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract CaSO3 is a by-product formed by several of the processes used for scrubbing SO2 from flue gas produced by coal-burning power generators. Using CaSO3 to improve the calcium status of acid soils would be a beneficial alternative to disposal in landfills. CaSO3 has biocidal properties and is used as a disinfectant and food and drink preservative. It is important to evaluate under what conditions application to soils would not harm plant growth. Laboratory experiments confirmed that two transformations of CaSO3 occurred in soil systems: (1) decomposition to produce SO2 gas, and (2) oxidation to calcium sulfate. Conversion to SO2 occurred in solution and soil at low pH, and acid soils treated with CaSO3 were initially toxic to seedling root growth. The degree of toxicity was time-dependent, with reduction in toxicity occurring as CaSO3 oxidized to calcium sulfate. Soil reaction also influenced toxicity, and at soil pH levels above 6, little seedling toxicity was evident.
    Type of Medium: Electronic Resource
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