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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 468 (1986), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0039-9140
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography B: Biomedical Sciences and Applications 661 (1994), S. 109-118 
    ISSN: 0378-4347
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 358 (1997), S. 670-676 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The paper describes the determination of tin by ASV using modified thick film electrodes. Three different types of electrodes were developed: One modified with a mixture of Nafion and mercury(II)acetate, one modified with diethyldithiocarbamate (DDC) or pyrrolidinedithiocarbamate (PDC) and mercury(II)acetate, and one modified with calomel. The analyte was accumulated on the electrode surface after special electrochemical pretreatment of the modified electrode. After recording the voltammogram the electrodes were electrochemically regenerated. By virtue of their lifetime and their measurement reproducibility, we preferred the DDC and PDC modified electrodes. They can be used for months without changing their chemical characteristics. The linear range for tin determination with these electrodes is between 1 and 100 μg/L; the detection limit was calculated as 0.9 μg/L. The electrodes were applied to the direct determination of tin in different canned fruit juices without special sample pretreatment.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A method has been developed to separate hydroxylated metabolites of the carcinogenic polycyclic aromatic hydrocarbon benzo[a]pyrene, i. e. trans-4,5-, 7,8-, 9,10-dihydrodiol and 1-, 3-, 7-, and 9-phenol, by HPLC with amperometric detection employing an isocratic methanol/water eluent (70:30, v/v) containing 0.5 g/L sulfuric acid and 1 g/L lithium perchlorate. Compared with the usually applied fluorescence (λex = 265 nm, λem = 460 nm) and ultraviolet (λ = 265 nm) detection, the amperometric technique is about 2–12 times more sensitive for the determination of all metabolites investigated. The method was applied to the determination of the seven metabolites of benzo[a]pyrene in different water samples and in urine after solid-phase extraction (SPE). The results obtained by HPLC with amperometric detection after SPE enrichment from an aqueous extract of a soil sample and from the urine of a rat intragastrically treated with benzo[a]pyrene agreed well with the values determined with fluorescence and/or UV detection.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 354 (1996), S. 11-15 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. A sensitive and selective adsorption stripping voltammetric (AdSV) method for the determination of antimony using chloranilic acid (2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone) as complexing reagent is described. The conditions under which its species of both oxidation states, Sb(III) and Sb(V), can be detected have been established. Sb(III) can be adsorbed onto the hanging mercury drop electrode (HMDE) using an accumulation potential of +100 mV from hydrochloric acid (pH=3.0) solution. Sb(V) can be determined using an accumulation potential of −500 mV in HCl (pH=1.0) solution. The peak potentials in the stripping voltammograms are −400 mV for Sb(III) and −140 mV for antimony (V). The detection limits are 210 ng/L for Sb(III) with 5 min pre-concentration and 560 ng/L for Sb(V) with 10 min pre-concentration. The method is applicable to the trace analysis and speciation of antimony in water samples and phosphoric acid.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 358 (1997), S. 741-744 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A voltammetric stripping procedure is described for the determination of arsenic(V) in a mannitol-sulphuric acid medium. The arsenic is coprecipitated with copper and selenium and reduced to arsine at the hanging mercury drop electrode. Using an accumulation time of 240 s, the detection limit is 0.52 μg L–1, the determination limit is 0.9 μg L–1. The method has been applied to the determination of arsenic in water samples. By varying the composition of the supporting electrolyte it is possible to differentiate between arsenic(III) and arsenic(V). As both oxidation states have different toxicological characteristics, the ability to discriminate between both is an distinct advantage of the proposed method.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' journal of analytical chemistry 364 (1999), S. 285-295 
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Various types of modified thick-film graphite electrodes are reviewed. Two modification options are available: either in situ modified or beforehand. Electrodes modified in situ by various organic compounds were used for the determination of W, Mo, Cr, Ni and Mn by adsorptive stripping voltammetry. Insoluble inorganic salts, insoluble organic complexes or soluble compounds protected with Nafion were used for modification of the electrode surface beforehand. These pre-conditioned electrodes permit quantification of Pb, Cd, Cu, Zn, Sn, As and Hg ions. The detection limits of these elements were in the sub-μg/L range. The relative standard deviation did not exceed 10–15%. Measurements were made without deaeration of test solutions and normally without destroying small organic matter found in surface waters. A number of characteristics, such as the formation of well-shaped peaks and stable increments of peaks after standard additions, as well as elimination of the mechanical surface regeneration stage and metallic mercury or its soluble salts from the analytical procedure and a long shelf-life of the electrodes make them promising for electroanalysis and for application in portable field instruments.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1041
    Keywords: Methotrexate ; folinic acid ; 7-hydroxymethotrexate ; pharmacokinetics ; 5-methyltetrahydrofolic acid ; leucovorin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Medicine
    Notes: Summary The pharmacokinetics of methotrexate (MTX), 7-hydroxymethotrexate (7-OHMTX), 2,4-diaminomethylpteroic acid (APA), folinic acid, and 5-methyltetrahydrofolate (5-MTHF) have been studied during 21 high-dose MTX (HDMTX) infusions (5 g·m−2 in 24 h) with leucovorin (LCV) rescue, a component of the therapy of 5 children with acute lymphoblastic leukemia (ALL). The median steady-state concentration of MTX was 66 μmol·l−1. Three elimination half-lifes were determined for MTX: 1.8 h, 6.4 h and a terminal 15 h. The median systemic MTX clearance was 110 mg·m−2·min−1. The 7-OHMTX level increased during each infusion and a Cmax of 19 μmol·l−1 was achieved at the end. Its initial half-life was 5 h and the terminal half-life was 12 h. Thus, the peak serum concentration ratio of 7-OHMTX to MTX was reached 24 h after the end of the infusion at a median ratio of 8. The MTX metabolite APA was detected in concentrations less than 0.06 μmol·l−1. The median folinic acid level during rescue, 48 h after starting the infusion, was 7.0 μmol·l−1 and 18 h following the last dose of LCV it was 0.44 μmol·l−1, leading to ratios of folinic acid to MTX of 31 and 6, respectively. The median 5-MTHF level during rescue was 0.44 μmol·l−1 with a median ratio of 5-MTHF to MTX of 2. Twenty infusions with 48 h MTX levels of less than 0.5 μmol·l−1 were without marked toxicity. Only one patient with a 48 h MTX concentration of 5.5 μmol·l−1 and a ratio of 5-MTHF to MTX of 0.08 suffered from ulcerating mucositis and septicaemia despite increased and prolonged LCV rescue.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 172 (1960), S. 409-413 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Zusammenfassung Stark salzsaure Wolframatlösungen lassen sich mit Zinkstaub quantitativ zu WIII reduzieren. Auf dieser Grundlage wird ein schnelles und genaues volumetrisches Verfahren zur Wolframbestimmung entwickelt. Bei geeigneter Arbeitsweise ist die Ausschaltung des Luftsauerstoffes nicht erforderlich. Die Titration erfolgt mit Cer(IV)-sulfat.
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