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  • 1
    ISSN: 1432-1904
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 28 (1989), S. 197-202 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin layer chromatography ; Piroxicam ; Piroxicam degradation products
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary HPTLC densitometry and HPLC are considered for the simultaneous determination of the degradation products of piroxicam (2-aminopyridine, DP-I and DP-II). The substances were separated on silica gel with fluorescence indicator in ethylacetate — toluene — diethylamine (10∶10∶5) and toluene — absolute ethanol — glacial acetic acid (8∶1.2∶0.5) systems. The measuring absorbance (detection of reflectance) of the separated substances was carried out “in situ” at 296 nm using 4-level calibration (external standard, nonlinear regresson function) in the concentration range 600–1200 ng 2-aminopyridine/spot and 300–600 ng DP-I and DP-II/spot. The HPLC method was carried out using RP-8 stationary phase and methanol + phosphate-citrate buffer, pH 3 mobile phase with addition of sodium pentanesulfonate (40+60, v/v). 2-aminopyridine wass detected at 300 nm, DP-I at 280 nm and DP-II at 248 nm. The concentration range for 2-aminopyridine is 2–40 μg/ml, for DP-I and DP-II 2–20 μg/ml (for an injection volume of 10 μl). The results were evaluated by linear regression analysis.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin layer chromatography ; Azidothymidine ; Thymine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary HPTLC densitometry and HPLC are considered for the determination of azidothymidine and its degradation product thymine in pharmaceutical dosage forms. In HPTLC the substances were separated on silica gel with fluorescence indicator in methanol-chloroform (10∶90) and methanol-chloroform (15∶85) systems. Absorbance measurement (detection of reflectance) of the separated substances was carried outin situ at 268 nm using four-level calibration (external standard, linear regression function) in the concentration range of 25–100 ng thymine/spot and using single-level calibration (external standard) at the concentration of 100 ng azidothymidine/spot. HPLC was carried out using RP-18 stationary phase and methanol+aqueous 0.03 mol/l KH2PO4 (18+82, v/v) as the mobile phase. The temperature was 50°C and the detection wavelength 266 nm. The detection limit of thymidine was 0.05%. The concentration range for azidothymidine was 0.5–1.5 mg/ml and for thymine 1–40 μg/ml (for an injection volume of 10 μl). The results were evaluated by linear regression analysis.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 29 (1990), S. 562-570 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Thin layer chromatography ; Azidothymidine ; Impurities of azidothymidine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary HPTLC densitometry and HPLC have been developed for the determination of potential impurities of azidothymidine (theymine, isothymidine, Az-Tr-thymidine, Ms-Tr-thymidine and Tr-alcohol). In HPTLC the substances were separated on silica gel with fluorescence indicator in 5∶95 methanol-chloroform for the simultaneous determination of Az-Tr-thymidine, Ms-Tr-thymidine and Tr-alcohol and in 10∶90 methanolchloroform for the simultaneous determination of thymine and isothymidine. Absorbance measurement (detection of reflectance) of separated substances was carried out “in situ” at 268 and 220 nm using four-level calibration (external standard) in the range of 25–100 ng thymine and isothymidine per spot. 50–200 ng Ms-Tr-thymidine and Az-Tr-thymidine per spot and 250–1000 ng Tr-alcohol per spot. For the HPLC determination of impurities two procedure are described one for thymine and isothymidine and the other for Ms-Tr-thymidine, Tr-alcohol and Az-Tr-thymidine. The first procedure was carried out using RP-18 stationary phase and methanol+aqueous 0.03 mol/l KH2PO4 (18+82, v/v) as the mobile phase. The temperature was 50°C and the detection wavelength 266 nm. In the second procedure the methanol content of the mobile phase was increased to 81% and the detection wavelength was changed to 210 nm. The detection limit of all impurities was 0.05 %. The concentration range for thymine was 1–40μg/ml and for the other impurities 1–20 μg/ml (for an injection volume of 10 μl). The results were evluated by linear regression analysis.
    Type of Medium: Electronic Resource
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