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  • Electronic Resource  (3)
  • 1995-1999  (3)
  • lithium chloride  (2)
  • Apoptosis  (1)
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  • Electronic Resource  (3)
Years
  • 1995-1999  (3)
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  • 1
    ISSN: 1572-879X
    Keywords: oxidative dehydrogenation ; ethane ; sulfated zirconia ; lithium chloride
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The oxidative dehydrogenation of ethane over sulfated-zirconia-supported lithium chloride catalysts has been systematically investigated. The optimal experimental parameters were obtained. It is found that sulfation of zirconia increases the catalytic activity. 2–3.5 wt% lithium chloride on sulfated zirconia catalysts exhibit high catalytic activity for oxidative dehydrogenation of ethane, with particularly high activity for ethene production. 70% selectivity to ethene at 98% ethane conversion, giving 68% ethene yield, is achieved over 3.5 wt% LiCl/SZ at 650°C.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-879X
    Keywords: sulfated zirconia ; lithium chloride ; metal oxides ; ethane ; oxidative dehydrogenation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effects of some transition‐ and lanthanide‐metal oxides in LiCl/sulfated‐zirconia (SZ) catalysts on catalytic behavior in the oxidative dehydrogenation of ethane were investigated. It is found that modification of LiCl/SZ by metal oxides significantly improves the catalytic activity and ethene yield. Among those additives, Ni and Nd oxides show the best promoting effect in terms of ethane conversion and ethene yield. 93% ethane conversion with 83% selectivity to ethene has been achieved over the Nd2O3–LiCl/SZ catalyst at 650°C. In addition, those oxide‐promoted LiCl/SZ catalysts are also found to exhibit a longer stability in catalytic performance. Metal‐oxide additives change the chemical structure and surface redox properties, which accounts for the enhancement of activity.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 139 (1997), S. 851-856 
    ISSN: 0942-0940
    Keywords: Apoptosis ; bromocriptine ; octreotide ; somatotropinoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Octreotide is a potent agonist of somatostatin that lowers the serum level of growth hormone (GH), and reduces the size of somatotropinomas. However, the detailed mechanism of shrinkage of this tumour is not known. We, therefore, evaluated 11 patients with somatotropinomas who were treated with octreotide 300 μg/day for 2–5 weeks to observe the morphological changes in the tumour using electron microscopy and the immunocytochemical study of apoptosis using polyclonal anti-single stranded DNA. Findings were compared with those obtained with bromocriptine treatment (10 mg/day, 2 weeks) of 5 patients with somatotropinomas, and 11 patients who received no preoperative treatment (control group). The octreotide group showed neither increase in stromal tissue nor cell death. The size of tumour cells appeared to be slightly reduced. No typical apoptotic bodies were seen on the electron micrographs. The apoptotic index in the octreotide group (0.40 ± 0.60%; mean ± SD) resembled that in the control group (0.81 ± 0.79%). In contast, the bromocriptine group showed some cell death and an increase in stromal tissue. The bromocriptine group also showed the apoptotic index which (20.1 ± 14.8%) was significantly higher than that of the control group (0.81 ± 0.79%). Thus, octreotide did not induce apoptosis in somatotropinomas despite the presence of tumour shrinkage. Because of the lack of fibrosis observed in the octreotide-treated tumours, the preoperative administration of octreotide may help to improve the outcome of the transsphenoidal operation.
    Type of Medium: Electronic Resource
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