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  • Articles: DFG German National Licenses  (6)
  • 1990-1994  (6)
  • 1955-1959
  • pancreas  (3)
  • supercritical fluid chromatography  (3)
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  • Articles: DFG German National Licenses  (6)
Material
Years
  • 1990-1994  (6)
  • 1955-1959
Year
  • 1
    ISSN: 1573-0646
    Keywords: phase II ; fazarabine ; adenocarcinoma ; pancreas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract We conducted a phase II evaluation of fazarabine 1.75–2.0 mg/m2hr over 72 hours every 28 days in 14 previously untreated patients with advanced adenocarcinoma of the pancreas. The intial dose was 1.75 mg/m2/hr in 10 patients, and 2.0 mg/m2hr in 4 patients. The dose was escalated in 8 patients, including all 4 who started at the higher dose level. Toxicity was unexpectedly mild. The median WBC nadir was 4.4 (range: 2.4–15.8)×103/μl, the median absolute neutrophil nadir was 3.2 (range: 0.9–13.0)×103/μl, and the median platelet count was 134.0 (range: 48.0–291.0)×103/μl. Gastrointestinal toxicity was generally mild. No major responses were seen, excluding, with 95% confidence, a response rate in excess of 20%.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Investigational new drugs 10 (1992), S. 313-316 
    ISSN: 1573-0646
    Keywords: phase II ; edatrexate ; adenocarcinoma ; pancreas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract We conducted a phase II evaluation of edatrexate in 17 previously untreated patients with advanced adenocarcinoma of the pancreas; 14 patients had at least one month of therapy. The initial dose was 80 mg/m2iv. Treatment was administered weekly for 5 weeks, then every other week. Toxicity was generally mild. The median WBC nadir was 5.4 (range 0.6–7.4)×103/μl, and the median platelet nadir was 164.0 (range 62.0–341.0)×103/μl. One patient died with sepsis and gastrointestinal bleeding associated with pancytopenia. Five patients had a mild rash. Nausea occurred in 6 patients, including 3 who had vomiting. In addition, 11 patients complained of vague malaise which seemed to begin within 24–48 hours after administration of edatrexate, and lasted for 2 to 3 days, resolving within 6 days of drug administration. Median survival was 85 days. Although 5 patients had stable disease, including one with relief of pain, no major responses were seen, excluding, with 95% confidence, a response rate in excess of 20%.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-0646
    Keywords: pancreas ; adenocarcinoma ; gemcitabine ; 2,2′-difluorodeoxycytidme ; phase II
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Abstract Gemcitabine is a novel nucleoside analog which demonstrated a broad spectrum of preclinical acitivity in solid tumor models, and responses in patients with pancreas cancer during phase I evaluation. Patients with measurable adenocarcinoma of the pancreas who had received no previous chemotherapy were eligible for this multicenter phase II clinical trial. Gemcitabine 800 mg/m2 was administered intravenously weekly for 3 consecutive weeks, followed by one week rest, every 4 weeks. Forty-four patients entered the trial; 35 had at least 2 cycles of therapy. Partial response was observed in 5 patients (11%, estimated 95% confidence interval 2–20%), with a median duration of 13 months. All responding patients had stabilization or improvement in performance status. Fourteen patients had stable disease of 4 or more months. The median WBC nadir was 3.8 × 103/μl (range 1.6–9.3) and the median absolute neutrophil (ANC) nadir was 2.0 × 103/μl (range 0.4–7.2). Thrombocytopenia - 100.0 × 103/μl was observed in 15 patients; the median platelet nadir was 123.0 (range 30.0–245.0). All patients experienced a mild to moderate flu-like syndrome. In addition, one patient had a mild hemolytic-uremic syndrome which appeared related to gemcitabine therapy. Gemcitabine demonstrated marginal activity in this resistant neoplasm, without excessive toxicity. Further evaluation, including the use of more intense dosing and/or combination therapy, is warranted.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 441-449 
    ISSN: 1040-7685
    Keywords: open-tubular columns ; supercritical fluid chromatography ; retention ; selectivity ; pressure ; temperature ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: We studied solute retention for n-hydrocarbons, (low-molecular-weight) polystyrenes, an ethoxylated surfactant, and a selectivity test mix on open-tubular columns with methyl-, biphenyl-, and cyanopropyl-substituted stationary phases for pressures up to 680 atm and temperatures up to 240°C. The solute elution range varied tremendously with column choice, with the least retentive stationary phases providing the highest elution range. However, the best resolution and largest analysis range were obtained with the most retentive stationary phase and the highest pressures. Increasing the temperatures above 160°C did not cause a large increase in elution pressure for the solutes used in this study. Exceptionally large shifts in selectivity with temperatures up to about 160°C occurred for the biphenyl and cyanopropyl stationary phases. The availability of pressures higher than 680 atm, coupled with adequately retentive stationary phases used at optimal temperatures, would further increase the analysis scope of opentubular supercritical fluid chromatography.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 261-273 
    ISSN: 1040-7685
    Keywords: open-tubular columns ; supercritical fluid chromatography ; direct injection ; phase behavior ; critical mixture curves ; retention gap ; solvent effect ; phase-ratio focusing ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Open-tubular supercritical fluid chromatography (SFC) is a useful technique for many analyses, but is somewhat limited, in current practice, with respect to trace analysis of liquid samples. Direct injection of the volumes required for trace analysis with ordinary detectors creates a meter or more length of flooded zone and may lead to unacceptable band broadening. We studied solvent mass transfer on short, uncoated columns for several solvents forming Type I binary mixtures with CO2, and found evidence in the solvent peak shapes of distinct liquid and vapor phases, with the liquid present as a dynamically formed film. This study suggests that selecting an injection temperature and pressure to reduce, but not eliminate, the surface tension of the liquidvapor interface, and increasing the mobile phase velocity during injection increase the liquid film thickness and reduce the length of the resulting flooded zone. When a separate uncoated inlet tube (that is, a retention gap) is used to connect the injector with the column, decreasing the inlet tube radius improves the ratio of maximum effective injection volume to inlet tube volume.Just as in GC, dynamically formed films function as pseudo-stationary phases during injection. Without a liquid film, solutes can be transported by injection-solvent-modified mobile phase well beyond the length of a typical film, increasing the difficulty of refocusing the solutes before separation. Refocusing solutes from film-coated flooded zones is easily accomplished using either a solvent effect (specifically, solvent trapping) or phase-ratio focusing.We recommend the use of solvents with phase behavior like toluene and carbon tetrachloride, both of which form films at convenient temperatures and pressures. We discourage the use of solvents with phase behavior like n-pentane which tend to make single-phase, supercritical mixtures with CO2 under typical SFC injection conditions.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 127-133 
    ISSN: 1040-7685
    Keywords: supercritical fluid chromatography ; retention mechanism ; selectivity tuning ; stationary phase swelling ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: When temperature programming is performed in supercritical fluid chromatography (SFC) under conditions where the solute-mobile phase interactions are approximately fixed, that is, with the use of constant mobile phase density, then positive temperature programs can be used. The results resemble those in temperature-programmed gas chromatography (GC) except that chromatograms are compressed and solutes elute at lower temperatures. For a given temperature-program rat, the extent of this compression effect is controlled by the (fixed) mobile phase density. When a methylsilicone stationary phase is used along with CO2 mobile phase, the compression occurs with little change in selectivity. However, with a biphenyl-substituted polysiloxane stationary phase, selectivity shifts occur for some solutes (vs. hydrocarbons) as the density is varied. The effect is even greater and affects more solutes when a cyanopropyl-substituted polysiloxane stationary phase is used.This selectivity behavior differs from the temperature-dependent selectivity behavior known in GC. In GC only the forces between solutes and the stationary phase are involved. But in SFC, mobile phase interactions with both the solutes and the stationary phase are also important. The large selectivity shifts we observe in SFC most likely arise because of stationary phase swelling by the mobile phase. This is a function of the temperature and mobile phase density (or pressure) and can be tuned without changing the composition of the mobile phase. It is possible to use either temperature or density to adjust or fine-tune selectivity between a pair of solutes while using the other parameter to adjust retention of the pair.These experiments further suggest that GC is not only a special case of SFC (where the solute-mobile phase interactions are essentially zero), but that SFC possesses an additional and extremely powerful selectivity adjustment mechanism not available in GC.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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