Ivanović, I

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  • Ivanović, I (4)
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Author's Bibliography

Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment

Živanović, L; Zečević, Mira; Marković, S; Petrović, S; Ivanović, I

(Elsevier Science BV, Amsterdam, 2005)

TY  - JOUR
AU  - Živanović, L
AU  - Zečević, Mira
AU  - Marković, S
AU  - Petrović, S
AU  - Ivanović, I
PY  - 2005
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/573
AB  - In this paper, there was developed a sensitive, precise and accurate reversed-phase liquid chromatographic (RP-HPLC) method and validated for simultaneous determination of lidocaine hydrochloride, dexamethasone acetate (DA) and calcium dobesilate (CD) in suppositories and ointment. Also there was achieved a parallel analysis of buthylhydroxyanisol, as a preservative, and hydroquinone, as a degradation product of calcium dobesilate, present in these dosage forms. The relative standard deviation (RSD) values for all five compounds indicated a good precision and accuracy of the RP-HPLC method. Method is selective, sensitive and reproducible with good recovery values and can be applied in simultaneous determination of all mentioned compounds.
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Chromatography A
T1  - Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment
VL  - 1088
IS  - 1-2
SP  - 182
EP  - 186
DO  - 10.1016/j.chroma.2005.04.049
ER  - 
@article{
author = "Živanović, L and Zečević, Mira and Marković, S and Petrović, S and Ivanović, I",
year = "2005",
abstract = "In this paper, there was developed a sensitive, precise and accurate reversed-phase liquid chromatographic (RP-HPLC) method and validated for simultaneous determination of lidocaine hydrochloride, dexamethasone acetate (DA) and calcium dobesilate (CD) in suppositories and ointment. Also there was achieved a parallel analysis of buthylhydroxyanisol, as a preservative, and hydroquinone, as a degradation product of calcium dobesilate, present in these dosage forms. The relative standard deviation (RSD) values for all five compounds indicated a good precision and accuracy of the RP-HPLC method. Method is selective, sensitive and reproducible with good recovery values and can be applied in simultaneous determination of all mentioned compounds.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Chromatography A",
title = "Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment",
volume = "1088",
number = "1-2",
pages = "182-186",
doi = "10.1016/j.chroma.2005.04.049"
}
Živanović, L., Zečević, M., Marković, S., Petrović, S.,& Ivanović, I.. (2005). Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment. in Journal of Chromatography A
Elsevier Science BV, Amsterdam., 1088(1-2), 182-186.
https://doi.org/10.1016/j.chroma.2005.04.049
Živanović L, Zečević M, Marković S, Petrović S, Ivanović I. Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment. in Journal of Chromatography A. 2005;1088(1-2):182-186.
doi:10.1016/j.chroma.2005.04.049 .
Živanović, L, Zečević, Mira, Marković, S, Petrović, S, Ivanović, I, "Validation of liquid chromatographic method for analysis of lidocaine hydrochloride, dexamethasone acetate, calcium dobesilate, buthylhydroxyanisol and degradation product hydroquinone in suppositories and ointment" in Journal of Chromatography A, 1088, no. 1-2 (2005):182-186,
https://doi.org/10.1016/j.chroma.2005.04.049 . .
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Stability testing of cefuroxime in tablets by micellar liquid chromatography

Živanović, L; Ivanović, I; Solomun, Ljiljana; Zečević, Mira

(Springer Heidelberg, Heidelberg, 2004)

TY  - JOUR
AU  - Živanović, L
AU  - Ivanović, I
AU  - Solomun, Ljiljana
AU  - Zečević, Mira
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/510
AB  - Cefuroxime is a broad-spectrum second-generation bactericidal cephalosporin antibiotic active against beta-lactamose-producing strains. Anti-cefuroxime, the geometric isomer of cefuroxime, might be present in cefuroxime dosage forms as a process-related impurity and possible degradation product. In the work discussed in this paper a precise and sensitive micellar liquid chromatographic (MLC) method for stability testing of cefuroxime axetil and anti-cefuroxime axetil in tablets, using benzoic acid as internal standard, was developed and validated. MLC was performed on an XTerra C-18 reversed-phase column at 50 degreesC with 8:92 (v/v) acetonitrile-20 mm sodium dodecyl sulphate, pH 2.5, as mobile phase at a flow rate of 1.5 mL min(-1). Detection was at 280 nm. Under these conditions the retention time and retention factor were of 6.65 min and 4.57, respectively, for cefuroxime axetil and 11.45 min and 8.59, respectively, for anti-cefuroxime axetil, indicating that the compounds were well separated. RSD values for quantification of cefuroxime axetil and anti-cefuroxime axetil were 0.39 and 1.7%, respectively, indicating the precision of the MLC method was good. The method is sensitive-LOD = 0.5 mug mL(-1) and LOQ = 1.5 mug mL(-1) for anti-cefuroxime axetil-and reproducible, with good recovery values.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - Stability testing of cefuroxime in tablets by micellar liquid chromatography
VL  - 60
IS  - SUPPL.
DO  - 10.1365/s10337-004-0237-5
ER  - 
@article{
author = "Živanović, L and Ivanović, I and Solomun, Ljiljana and Zečević, Mira",
year = "2004",
abstract = "Cefuroxime is a broad-spectrum second-generation bactericidal cephalosporin antibiotic active against beta-lactamose-producing strains. Anti-cefuroxime, the geometric isomer of cefuroxime, might be present in cefuroxime dosage forms as a process-related impurity and possible degradation product. In the work discussed in this paper a precise and sensitive micellar liquid chromatographic (MLC) method for stability testing of cefuroxime axetil and anti-cefuroxime axetil in tablets, using benzoic acid as internal standard, was developed and validated. MLC was performed on an XTerra C-18 reversed-phase column at 50 degreesC with 8:92 (v/v) acetonitrile-20 mm sodium dodecyl sulphate, pH 2.5, as mobile phase at a flow rate of 1.5 mL min(-1). Detection was at 280 nm. Under these conditions the retention time and retention factor were of 6.65 min and 4.57, respectively, for cefuroxime axetil and 11.45 min and 8.59, respectively, for anti-cefuroxime axetil, indicating that the compounds were well separated. RSD values for quantification of cefuroxime axetil and anti-cefuroxime axetil were 0.39 and 1.7%, respectively, indicating the precision of the MLC method was good. The method is sensitive-LOD = 0.5 mug mL(-1) and LOQ = 1.5 mug mL(-1) for anti-cefuroxime axetil-and reproducible, with good recovery values.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "Stability testing of cefuroxime in tablets by micellar liquid chromatography",
volume = "60",
number = "SUPPL.",
doi = "10.1365/s10337-004-0237-5"
}
Živanović, L., Ivanović, I., Solomun, L.,& Zečević, M.. (2004). Stability testing of cefuroxime in tablets by micellar liquid chromatography. in Chromatographia
Springer Heidelberg, Heidelberg., 60(SUPPL.).
https://doi.org/10.1365/s10337-004-0237-5
Živanović L, Ivanović I, Solomun L, Zečević M. Stability testing of cefuroxime in tablets by micellar liquid chromatography. in Chromatographia. 2004;60(SUPPL.).
doi:10.1365/s10337-004-0237-5 .
Živanović, L, Ivanović, I, Solomun, Ljiljana, Zečević, Mira, "Stability testing of cefuroxime in tablets by micellar liquid chromatography" in Chromatographia, 60, no. SUPPL. (2004),
https://doi.org/10.1365/s10337-004-0237-5 . .
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Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer

Živanović, L; Ivanović, I; Vladimirov, S; Zečević, Mira

(Elsevier Science BV, Amsterdam, 2004)

TY  - JOUR
AU  - Živanović, L
AU  - Ivanović, I
AU  - Vladimirov, S
AU  - Zečević, Mira
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/535
AB  - The optimal chromatographic conditions for the separation of the syn- and anti-geometric isomers of cefuroxime axetil applying RP-HPLC and micellar liquid chromatography (MLC) methods were investigated. The possibility to separate diastereoisomers of syn- and anti-cefuroxime axetil was observed. Investigations were performed using three columns, two classical silicas and one with hybrid particle technology. Three aqueous-organic and one micellar mobile phases were used. The best results were achieved using micellar mobile phase. Optimization study was performed using different micellar mobile phases. MLC method is sensitive and applicable in purity and stability testing.
PB  - Elsevier Science BV, Amsterdam
T2  - Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences
T1  - Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer
VL  - 800
IS  - 1-2
SP  - 175
EP  - 179
DO  - 10.1016/j.jchromb.2003.08.046
ER  - 
@article{
author = "Živanović, L and Ivanović, I and Vladimirov, S and Zečević, Mira",
year = "2004",
abstract = "The optimal chromatographic conditions for the separation of the syn- and anti-geometric isomers of cefuroxime axetil applying RP-HPLC and micellar liquid chromatography (MLC) methods were investigated. The possibility to separate diastereoisomers of syn- and anti-cefuroxime axetil was observed. Investigations were performed using three columns, two classical silicas and one with hybrid particle technology. Three aqueous-organic and one micellar mobile phases were used. The best results were achieved using micellar mobile phase. Optimization study was performed using different micellar mobile phases. MLC method is sensitive and applicable in purity and stability testing.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences",
title = "Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer",
volume = "800",
number = "1-2",
pages = "175-179",
doi = "10.1016/j.jchromb.2003.08.046"
}
Živanović, L., Ivanović, I., Vladimirov, S.,& Zečević, M.. (2004). Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer. in Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences
Elsevier Science BV, Amsterdam., 800(1-2), 175-179.
https://doi.org/10.1016/j.jchromb.2003.08.046
Živanović L, Ivanović I, Vladimirov S, Zečević M. Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer. in Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences. 2004;800(1-2):175-179.
doi:10.1016/j.jchromb.2003.08.046 .
Živanović, L, Ivanović, I, Vladimirov, S, Zečević, Mira, "Investigation of chromatographic conditions for the separation of cefuroxime axetil and its geometric isomer" in Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, 800, no. 1-2 (2004):175-179,
https://doi.org/10.1016/j.jchromb.2003.08.046 . .
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Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain

Zečević, Mira; Minić, D; Stojšić, D.; Živanović, LJ; Ivanović, I

(Govi-Verlag Gmbh, Eschborn, 2004)

TY  - JOUR
AU  - Zečević, Mira
AU  - Minić, D
AU  - Stojšić, D.
AU  - Živanović, LJ
AU  - Ivanović, I
PY  - 2004
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/498
AB  - Ochratoxin A is a mycotoxin, a natural product of Aspergillus and Penicillium species. It can be present in grain from Triticum aestivum, (Graminae) and other starch-abundant cereals. This paper describes the investigation of ochratoxin A in grain from Triticum aestivum using a statistically optimized HPLC method. The assay was developed using two mathematical statistical models: factorial design and response surface mapping. The final step was to optimize the values of variables by response surface design. The analysis of variance 'ANOVA' method was applied to the analytical results in order to construct an adequate model. The optimal experimental conditions obtained by the response surface diagram method were: pH = 2.5, composition of the mobile phase acetonitrile: water 55:45 v/v and flow rate 1.0 ml/min. with a C18 column. Retention time and capacity factor for ochratotoxin A were 7.46 min. and 1.19, respectively.
PB  - Govi-Verlag Gmbh, Eschborn
T2  - Pharmazie
T1  - Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain
VL  - 59
IS  - 3
SP  - 175
EP  - 177
UR  - https://hdl.handle.net/21.15107/rcub_farfar_498
ER  - 
@article{
author = "Zečević, Mira and Minić, D and Stojšić, D. and Živanović, LJ and Ivanović, I",
year = "2004",
abstract = "Ochratoxin A is a mycotoxin, a natural product of Aspergillus and Penicillium species. It can be present in grain from Triticum aestivum, (Graminae) and other starch-abundant cereals. This paper describes the investigation of ochratoxin A in grain from Triticum aestivum using a statistically optimized HPLC method. The assay was developed using two mathematical statistical models: factorial design and response surface mapping. The final step was to optimize the values of variables by response surface design. The analysis of variance 'ANOVA' method was applied to the analytical results in order to construct an adequate model. The optimal experimental conditions obtained by the response surface diagram method were: pH = 2.5, composition of the mobile phase acetonitrile: water 55:45 v/v and flow rate 1.0 ml/min. with a C18 column. Retention time and capacity factor for ochratotoxin A were 7.46 min. and 1.19, respectively.",
publisher = "Govi-Verlag Gmbh, Eschborn",
journal = "Pharmazie",
title = "Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain",
volume = "59",
number = "3",
pages = "175-177",
url = "https://hdl.handle.net/21.15107/rcub_farfar_498"
}
Zečević, M., Minić, D., Stojšić, D., Živanović, L.,& Ivanović, I.. (2004). Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain. in Pharmazie
Govi-Verlag Gmbh, Eschborn., 59(3), 175-177.
https://hdl.handle.net/21.15107/rcub_farfar_498
Zečević M, Minić D, Stojšić D, Živanović L, Ivanović I. Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain. in Pharmazie. 2004;59(3):175-177.
https://hdl.handle.net/21.15107/rcub_farfar_498 .
Zečević, Mira, Minić, D, Stojšić, D., Živanović, LJ, Ivanović, I, "Application of experimental design to the development of an HPLC method for the analysis of ochratoxin A in Triticum aestivum grain" in Pharmazie, 59, no. 3 (2004):175-177,
https://hdl.handle.net/21.15107/rcub_farfar_498 .
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