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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 39 (1993), S. 107-135 
    ISSN: 1573-4889
    Keywords: sulphidation ; sulphides ; Co-base alloys ; (Fe, Co)-base alloys ; refractory metals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The sulphidation behavior of a series ofMCrAlYX-type alloys, where M is Co or Co and Fe, and X is V, Nb, Mo, or W, added in combination at various levels, has been studied at 750°C in an atmosphere of $$p_{S_2 } $$ ∼ 10−1 Pa and $$p_{O_2 } $$ ∼10−18 Pa. Sulphidation kinetics followed a parabolic rate law for each alloy over prolonged periods of exposure (up to 240 hr). Inclusion of Mo in the alloy containing both V and Nb, and particularly the combined additions of Mo and W, greatly enhanced sulphidation resistance. Partial replacement of Co by Fe also provided superior sulphidation resistance. The scales formed on the Co-based alloys consisted of three subscale layers-an outer layer of Co9S8 and Co3S4, a mid-layer of Cr3S4 and an inner layer of chromium and refractory-metal sulphides. In the case of (Fe, Co)-based alloys, the scales were duplex in nature with an outer layer of Fe3S4, Co9S8 and Cr3S4 and a compact inner layer consisting of sulphides of chromium and refractory metals. For both categories of alloys, the inner layer of refractory-metal sulphides was decorated by an alumina film which inhibited the outward migration of the base elements.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-0646
    Keywords: Fostriecin ; Hepsulfam ; PZDT ; hematopoietic progenitors ; human ; murine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The in vitro myelotoxic potentials of three investigational antitumor agents, Fostriecin, Hepsulfam and pyrazine diazohydroxide (PZDH), were evaluated utilizing clonogenic assays. Human and murine marrow cells were exposed to each drug for 1 hr prior to culture in microcapillary (human) or Petri dish (murine) assays. Fostriecin (0.22–220 μM), Hepsulfam (0.34–340 μM) and PZDH (0.68–680 μM) inhibited myeloid (CFU-gm), erythroid (BFU-e, CFU-e) and megakaryocytic (CFU-meg) colony formation in a concentration-dependent manner. CFU-e from both species were more sensitive to Fostriecin than the other progenitors and murine cells more sensitive overall to Fostriecin than their human counterparts. Murine CFU-e were also more sensitive to Hepsulfam than human CFU-e, with CFU-gm and BFU-e being similarly affected in both species. Human BFU-e were greatly inhibited by PZDH, whereas murine BFU-e were relatively resistant to its toxic effects. Fostriecin was the most toxic of the three antitumor agents, with PZDH the least toxic.
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  • 3
    ISSN: 1573-0646
    Keywords: FCE 24517 ; myelotoxicity ; in vitro ; human ; canine ; murine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary FCE 24517, a derivative of distamycin A, exhibits an unusual antitumor profile in experimental models. As part of its preclinical development, we evaluated thein vitro myelotoxicity of FCE 24517 to human, canine and murine hematopoietic cells. Marrow cells were exposed to the agent (2.7×10−5−2.7 nM) for 4 h and then assayed in capillary (human) or Petri dish (canine, murine) clonal cultures. FCE 24517 inhibited myeloid (CFU-gm), erythroid (BFU-e, CFU-e) and megakaryocytic (CFU-meg) colony formation in a concentration-dependent manner. The progenitor cells were generally similar in their response to FCE 24517 within a species. Comparing the different progenitor cell response to FCE 24517, canine CFU-gm and CFU-e were 26- to 221-fold more sensitive to this drug's toxic effects than their human and murine counterparts. This was demonstrated by extremely low IC70 values for the canine CFU-gm (0.001 nM) and CFU-e (0.007 nM). Murine progenitors displayed 1.3- to 10.9-times higher IC70 values than human CFU-gm, BFU-e and CFU-e following 4 hr exposure to FCE 24517. The data demonstrated that a mouse model may better predict humanin vitro myelotoxicity to FCE 24517 than beagle dogs.
    Type of Medium: Electronic Resource
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