Živanov-Stakić, Dobrila

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  • Živanov-Stakić, Dobrila (3)
Projects

Author's Bibliography

Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations

Marinković, Valentina D.; Milojković, Smiljana S.; Nedeljković, Jovan; Čomor, Jožef J.; Agbaba, Danica; Živanov-Stakić, Dobrila

(1997)

TY  - JOUR
AU  - Marinković, Valentina D.
AU  - Milojković, Smiljana S.
AU  - Nedeljković, Jovan
AU  - Čomor, Jožef J.
AU  - Agbaba, Danica
AU  - Živanov-Stakić, Dobrila
PY  - 1997
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2099
AB  - A straightforward quantitative method for gas chromatography-mass spectrometry determination of isosorbide 5-mononitrate (ISSMN) and its related impurities such as isosorbide (IS), isosorbide diacetate (ISDA) and isosorbide 2-acetate-5-nitrate (IS2A5N) in raw materials as well as in dosage formulations is developed. The recovery of these materials was found to be 100.4 +/- 2.4, 99.3 +/- 4.7, 97.8 +/- 5.2 and 100.1 +/- 3.1%, while the detection limits were 27.2, 1.26, 1.02 and 0.78 mu g in dosage formulations for ISSMN, ISDA, IS2A5N, and IS, respectively. The applicability of the method was tested by analysing three different formulations of ISSMN. (C) 1997 Elsevier Science B.V.
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations
VL  - 16
IS  - 3
SP  - 425
EP  - 429
DO  - 10.1016/S0731-7085(97)00079-4
ER  - 
@article{
author = "Marinković, Valentina D. and Milojković, Smiljana S. and Nedeljković, Jovan and Čomor, Jožef J. and Agbaba, Danica and Živanov-Stakić, Dobrila",
year = "1997",
abstract = "A straightforward quantitative method for gas chromatography-mass spectrometry determination of isosorbide 5-mononitrate (ISSMN) and its related impurities such as isosorbide (IS), isosorbide diacetate (ISDA) and isosorbide 2-acetate-5-nitrate (IS2A5N) in raw materials as well as in dosage formulations is developed. The recovery of these materials was found to be 100.4 +/- 2.4, 99.3 +/- 4.7, 97.8 +/- 5.2 and 100.1 +/- 3.1%, while the detection limits were 27.2, 1.26, 1.02 and 0.78 mu g in dosage formulations for ISSMN, ISDA, IS2A5N, and IS, respectively. The applicability of the method was tested by analysing three different formulations of ISSMN. (C) 1997 Elsevier Science B.V.",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations",
volume = "16",
number = "3",
pages = "425-429",
doi = "10.1016/S0731-7085(97)00079-4"
}
Marinković, V. D., Milojković, S. S., Nedeljković, J., Čomor, J. J., Agbaba, D.,& Živanov-Stakić, D.. (1997). Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations. in Journal of Pharmaceutical and Biomedical Analysis, 16(3), 425-429.
https://doi.org/10.1016/S0731-7085(97)00079-4
Marinković VD, Milojković SS, Nedeljković J, Čomor JJ, Agbaba D, Živanov-Stakić D. Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations. in Journal of Pharmaceutical and Biomedical Analysis. 1997;16(3):425-429.
doi:10.1016/S0731-7085(97)00079-4 .
Marinković, Valentina D., Milojković, Smiljana S., Nedeljković, Jovan, Čomor, Jožef J., Agbaba, Danica, Živanov-Stakić, Dobrila, "Gas chromatography mass spectrometry determination of isosorbide 5-mononitrate and related impurities in raw materials and dosage formulations" in Journal of Pharmaceutical and Biomedical Analysis, 16, no. 3 (1997):425-429,
https://doi.org/10.1016/S0731-7085(97)00079-4 . .
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Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine

Vladimirov, Sote; Čudina, Olivera; Agbaba, Danica; Jovanovic, M; Živanov-Stakić, Dobrila

(1996)

TY  - JOUR
AU  - Vladimirov, Sote
AU  - Čudina, Olivera
AU  - Agbaba, Danica
AU  - Jovanovic, M
AU  - Živanov-Stakić, Dobrila
PY  - 1996
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7217
AB  - The proposed method is based on coloured hydrazone formation with 1,4-dihydrazinophthalazine as a reagent. Heating at 85 degrees C for 2 h was found necessary to ensure optimal hydrazone formation in the presence of hydrochloric acid. The yellow hydrazone product has an absorption maximum at 380 nm. A linear relationship between absorbance and concentration was established in the concentration range 3.19 x 10(-6)-3.19 x 10(-5) mol l(-1) (the regression equation was y = 0.013 167 3 + 0.019 025 9x; correlation coefficient r = 0.9991; n = 6). The detection limit was 1.2 mu g ml(-1) (molar absorptivity found was 1.97 x 10(4) l mol(-1) cm(-1)). The reliability of the proposed method was checked at three different concentrations; the relative standard deviation (RSD) varied from 1.03 to 2.01%. The described method applied to the determination of desoximetasone in ointment gave precise and reproducible results; the recovery was 98.55% with RSD = 2.40% (n = 10).
T2  - Journal of Pharmaceutical and Biomedical Analysis
T1  - Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine
VL  - 14
IS  - 8-10
SP  - 947
EP  - 950
DO  - 10.1016/0731-7085(95)01681-3
ER  - 
@article{
author = "Vladimirov, Sote and Čudina, Olivera and Agbaba, Danica and Jovanovic, M and Živanov-Stakić, Dobrila",
year = "1996",
abstract = "The proposed method is based on coloured hydrazone formation with 1,4-dihydrazinophthalazine as a reagent. Heating at 85 degrees C for 2 h was found necessary to ensure optimal hydrazone formation in the presence of hydrochloric acid. The yellow hydrazone product has an absorption maximum at 380 nm. A linear relationship between absorbance and concentration was established in the concentration range 3.19 x 10(-6)-3.19 x 10(-5) mol l(-1) (the regression equation was y = 0.013 167 3 + 0.019 025 9x; correlation coefficient r = 0.9991; n = 6). The detection limit was 1.2 mu g ml(-1) (molar absorptivity found was 1.97 x 10(4) l mol(-1) cm(-1)). The reliability of the proposed method was checked at three different concentrations; the relative standard deviation (RSD) varied from 1.03 to 2.01%. The described method applied to the determination of desoximetasone in ointment gave precise and reproducible results; the recovery was 98.55% with RSD = 2.40% (n = 10).",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
title = "Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine",
volume = "14",
number = "8-10",
pages = "947-950",
doi = "10.1016/0731-7085(95)01681-3"
}
Vladimirov, S., Čudina, O., Agbaba, D., Jovanovic, M.,& Živanov-Stakić, D.. (1996). Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine. in Journal of Pharmaceutical and Biomedical Analysis, 14(8-10), 947-950.
https://doi.org/10.1016/0731-7085(95)01681-3
Vladimirov S, Čudina O, Agbaba D, Jovanovic M, Živanov-Stakić D. Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine. in Journal of Pharmaceutical and Biomedical Analysis. 1996;14(8-10):947-950.
doi:10.1016/0731-7085(95)01681-3 .
Vladimirov, Sote, Čudina, Olivera, Agbaba, Danica, Jovanovic, M, Živanov-Stakić, Dobrila, "Spectrophotometric determination of desoximetasone in ointment using 1,4-dihydrazinophthalazine" in Journal of Pharmaceutical and Biomedical Analysis, 14, no. 8-10 (1996):947-950,
https://doi.org/10.1016/0731-7085(95)01681-3 . .
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4

Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA

Jovanović, Moma S.; Vuksanovic, L; Brborić, Jasmina; Vladimirov, Sote; Živanov-Stakić, Dobrila

(1996)

TY  - JOUR
AU  - Jovanović, Moma S.
AU  - Vuksanovic, L
AU  - Brborić, Jasmina
AU  - Vladimirov, Sote
AU  - Živanov-Stakić, Dobrila
PY  - 1996
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/2027
T2  - Jugoslovenska Medicinska Biohemija
T1  - Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA
VL  - 15
IS  - 4
SP  - 266
EP  - 266
UR  - https://hdl.handle.net/21.15107/rcub_vinar_2027
ER  - 
@article{
author = "Jovanović, Moma S. and Vuksanovic, L and Brborić, Jasmina and Vladimirov, Sote and Živanov-Stakić, Dobrila",
year = "1996",
journal = "Jugoslovenska Medicinska Biohemija",
title = "Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA",
volume = "15",
number = "4",
pages = "266-266",
url = "https://hdl.handle.net/21.15107/rcub_vinar_2027"
}
Jovanović, M. S., Vuksanovic, L., Brborić, J., Vladimirov, S.,& Živanov-Stakić, D.. (1996). Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA. in Jugoslovenska Medicinska Biohemija, 15(4), 266-266.
https://hdl.handle.net/21.15107/rcub_vinar_2027
Jovanović MS, Vuksanovic L, Brborić J, Vladimirov S, Živanov-Stakić D. Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA. in Jugoslovenska Medicinska Biohemija. 1996;15(4):266-266.
https://hdl.handle.net/21.15107/rcub_vinar_2027 .
Jovanović, Moma S., Vuksanovic, L, Brborić, Jasmina, Vladimirov, Sote, Živanov-Stakić, Dobrila, "Interaction of Tc-99m-IODIDE IDA derivatives substituted with HSA" in Jugoslovenska Medicinska Biohemija, 15, no. 4 (1996):266-266,
https://hdl.handle.net/21.15107/rcub_vinar_2027 .