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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochemical and Biophysical Research Communications 97 (1980), S. 962-967 
    ISSN: 0006-291X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Plant Science Letters 23 (1981), S. 71-80 
    ISSN: 0304-4211
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1437-1596
    Keywords: Capillary gas chromatography, opiates ; Drug screening, determination of capillary gas chromatography ; Capillargaschromatographie ; Opiatnachweis ; Drogenscreening ; Capillargaschromatographie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Law
    Description / Table of Contents: Zusammenfassung Es wird eine Capillargaschromatographische Methode zur simultanen Bestimmung von Morphin, Codein, Heroin, 3- und 6-Monoacetylmorphin, Nalorphin, Naloxone, Naltrexon und Ethylmorphin beschrieben. Von 2ml Plasma, Urin oder anderen biologischen Proben (z.B. Gewebepräparate) wurden die Substanzen in alkalischen Milieu durch Chloroform: isopropylalkohol:n-heptan extrahiert, anschließend in Chloroform rückextrahiert. Nach Derivatiesierung mittels Trifluoressigsäureanhydrid wurden die aliquoten Teile an einer 25 m Capillarsäule eingesetzt. Die Detektion erfolgte durch einen Nitrogen-Phosphorous Detektor, und die Nachweisgrenzen und Wiederfindungsraten wurden ebenfalls ermittelt.
    Notes: Summary A capillary column gas chromatographic method is described for the simultaneous determination of morphine, codeine, heroin, 3- and 6-monoacetylmorphine, nalorphine, naloxone, ethylmorphine, and naltrexone. The drugs were extracted from 2ml plasma, urine, or other biological samples, including tissue under alkaline conditions in chloroform-isopropanol-n-heptane (50∶17∶33, v/v), with levallorphan as an internal standard. The drugs were extracted into acid and then reextracted into chloroform after the acid had been alkalinized. After derivatization with trifluoroacetic anhydride, an aliquot was injected into a 25m capillary column equipped with a nitrogen phosphorus detector. The lower limits of detectability, extraction recovery, and the within-run and day-to-day precision of results were determined for each drug. Our results indicate that the procedure is suitable for use in overdose screening and therapeutic drug monitoring.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    European journal of clinical pharmacology 37 (1989), S. 531-532 
    ISSN: 1432-1041
    Keywords: heroin ; 6-monoacetylmorphine ; capillary gas chromatography ; selected ion monitoring ; GC/MS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary A capillary gas chromatography mass spectrometry assay has been developed for the determination of 6-monoacetylmorphine in human urine, which is a confirmatory marker of heroin abuse. It was extracted with chloroform-isopropanol-n-heptane (50:17:33, v/v) from alkalinized samples (pH 9.2), using levallorphan as the internal standard. After derivatization with trifluoroacetic anhydride, the drugs were separated on a 25-m capillary column BP 10 and detected by selected ion monitoring.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-4838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Twenty-four-hour urinary mercury concentration were assessed in 43 patients before and after removing old amalgam fillings (8 pts), placing (13 pts), and polishing of amalgam (22 pts). Baseline analyses 8 days before the treatments showed on average 18.5±7.2 μg mercury mass excreted per 24-h urine samples. The removal of old fillings caused a total excreted mass of 56.3±32.3 μg Hg, the placing of amalgam 45.9±26.2 μg Hg, and the polishing 56.25±33.77 μg Hg, respectively, one day after the treatments. When compared with the baseline values, the urinary mass excreted remained significantly elevated during the 8-day follow-up. However, all Hg values measured were below the WHO recommandations for the threshold limits for urinary mercury.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 332 (1988), S. 468-469 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1437-1596
    Keywords: Capillary gas chromatography ; opiates ; Drug screening ; determination of capillary gas chromatography ; Capillargaschromatographie ; Opiatnachweis ; Drogenscreening ; Capillargaschromatographie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Law
    Description / Table of Contents: Zusammenfassung Es wird eine Capillargaschromatographische Methode zur simultanen Bestimmung von Morphin, Codein, Heroin, 3- und 6-Mono-acetylmorphin, Nalorphin, Naloxone, Naltrexon und Ethylmorphin beschrieben. Von 2 ml Plasma, Urin oder anderen biologischen Proben (z. B. Gewebepräparate) wurden die Substanzen in alkalischen Milieu durch Chloroform: isopropylalkohol: n-heptan extrahiert, anschließend in Chloroform rückextrahiert. Nach Derivatiesierung mittels Trifluoressigsäureanhydrid wurden die aliquoten Teile an einer 25 m Capillarsäule eingesetzt. Die Detektion erfolgte durch einen Nitrogen-Phosphorous Detektor, und die Nachweisgrenzen und Wiederfindungsraten wurden ebenfalls ermittelt.
    Notes: Summary A capillary column gas chromatographic method is described for the simultaneous determination of morphine, codeine, heroin, 3- and 6-monoacetylmorphine, nalorphine, naloxone, ethylmorphine, and naltrexone. The drugs were extracted from 2 ml plasma, urine, or other biological samples, including tissue under alkaline conditions in chloroform-isopropanol-n-heptane (50:17:33, v/v), with levallorphan as an internal standard. The drugs were extracted into acid and then reextracted into chloroform after the acid had been alkalinized. After derivatization with trifluoroacetic anhydride, an aliquot was injected into a 25m capillary column equipped with a nitrogen phosphorus detector. The lower limits of detectability, extraction recovery, and the within-run and day-to-day precision of results were determined for each drug. Our results indicate that the procedure is suitable for use in overdose screening and therapeutic drug monitoring.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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