Sljivić, Jasmina

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  • Sljivić, Jasmina (3)
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Author's Bibliography

Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability

Otašević, Biljana; Sljivić, Jasmina; Protić, Ana; Maljurić, Nevena; Malenović, Anđelija; Zečević, Mira

(Elsevier Science BV, Amsterdam, 2019)

TY  - JOUR
AU  - Otašević, Biljana
AU  - Sljivić, Jasmina
AU  - Protić, Ana
AU  - Maljurić, Nevena
AU  - Malenović, Anđelija
AU  - Zečević, Mira
PY  - 2019
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3304
AB  - The development of stability-indicating method with isocratic elution mode based on micellar liquid chromatography for the analysis of cilazapril, hydrochlorothiazide and their degradation products was the primary aim of the present research. Since this could be done using different methodologies, two approaches were selected and comprehensively compared. The first one was risk based quality by design concept adopted by many analysts since it ensures development of robust analytical methods. The second one was multicriteria decision making approach currently interpreted in a form of experimental design complemented with grid point search is well established over past decades as a very useful way to govern analytical method development. Major drawback of later approach, related to method robustness evaluation, was discounted through proposition of simple and efficient computational procedure. Both methodologies ultimately resulted in successful chromatographic separations of all investigated substances which included analysis on XTerra RP 18 (3.9 x 150 mm, 5 mu m) column with temperature set at 30 degrees C, mobile phase consisting of acetonitrile and Brij L23 aqueous solution (18 mmol L-1, pH 3.8) in ratio 13:87 (%, v/v) pumped at 1 mL min(-1) flow rate while UV detection was performed at 215 nm. Both the 3D representation of a design space as well as grid obtained with later approach pointed out that the method performance criteria would not be compromised when amount of acetonitrile amount varies in range 12-14% (v/v), pH of the water phase in range 3.4-4.0, while concentration of Brij L23 aqueous solution can be within 15-20 mmol L-1. Hence, although the method development was based on different starting hypothesis, both methodologies enabled achievement of reliable and robust analytical methods that could serve in monitoring of cilazaprile and hydrochlorothiazide combined dosage form stability.
PB  - Elsevier Science BV, Amsterdam
T2  - Microchemical Journal
T1  - Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability
VL  - 145
SP  - 655
EP  - 663
DO  - 10.1016/j.microc.2018.11.033
ER  - 
@article{
author = "Otašević, Biljana and Sljivić, Jasmina and Protić, Ana and Maljurić, Nevena and Malenović, Anđelija and Zečević, Mira",
year = "2019",
abstract = "The development of stability-indicating method with isocratic elution mode based on micellar liquid chromatography for the analysis of cilazapril, hydrochlorothiazide and their degradation products was the primary aim of the present research. Since this could be done using different methodologies, two approaches were selected and comprehensively compared. The first one was risk based quality by design concept adopted by many analysts since it ensures development of robust analytical methods. The second one was multicriteria decision making approach currently interpreted in a form of experimental design complemented with grid point search is well established over past decades as a very useful way to govern analytical method development. Major drawback of later approach, related to method robustness evaluation, was discounted through proposition of simple and efficient computational procedure. Both methodologies ultimately resulted in successful chromatographic separations of all investigated substances which included analysis on XTerra RP 18 (3.9 x 150 mm, 5 mu m) column with temperature set at 30 degrees C, mobile phase consisting of acetonitrile and Brij L23 aqueous solution (18 mmol L-1, pH 3.8) in ratio 13:87 (%, v/v) pumped at 1 mL min(-1) flow rate while UV detection was performed at 215 nm. Both the 3D representation of a design space as well as grid obtained with later approach pointed out that the method performance criteria would not be compromised when amount of acetonitrile amount varies in range 12-14% (v/v), pH of the water phase in range 3.4-4.0, while concentration of Brij L23 aqueous solution can be within 15-20 mmol L-1. Hence, although the method development was based on different starting hypothesis, both methodologies enabled achievement of reliable and robust analytical methods that could serve in monitoring of cilazaprile and hydrochlorothiazide combined dosage form stability.",
publisher = "Elsevier Science BV, Amsterdam",
journal = "Microchemical Journal",
title = "Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability",
volume = "145",
pages = "655-663",
doi = "10.1016/j.microc.2018.11.033"
}
Otašević, B., Sljivić, J., Protić, A., Maljurić, N., Malenović, A.,& Zečević, M.. (2019). Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability. in Microchemical Journal
Elsevier Science BV, Amsterdam., 145, 655-663.
https://doi.org/10.1016/j.microc.2018.11.033
Otašević B, Sljivić J, Protić A, Maljurić N, Malenović A, Zečević M. Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability. in Microchemical Journal. 2019;145:655-663.
doi:10.1016/j.microc.2018.11.033 .
Otašević, Biljana, Sljivić, Jasmina, Protić, Ana, Maljurić, Nevena, Malenović, Anđelija, Zečević, Mira, "Comparison of AQbD and grid point search methodology in the development of micellar HPLC method for the analysis of cilazapril and hydrochlorothiazide dosage form stability" in Microchemical Journal, 145 (2019):655-663,
https://doi.org/10.1016/j.microc.2018.11.033 . .
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Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods

Sljivić, Jasmina; Protić, Ana; Malenović, Anđelija; Otašević, Biljana; Zečević, Mira

(Springer Heidelberg, Heidelberg, 2018)

TY  - JOUR
AU  - Sljivić, Jasmina
AU  - Protić, Ana
AU  - Malenović, Anđelija
AU  - Otašević, Biljana
AU  - Zečević, Mira
PY  - 2018
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/3208
AB  - In this paper, an efficient way for robustness testing of gradient elution liquid chromatographic methods is proposed and tested on model mixtures comprising cilazapril, hydrochlorothiazide, and their degradation products, solutes that differ not only in polarities, but also in solubility and absorption characteristics. In general, the robustness could be tested with respect to various responses: resolution, retention factor, selectivity factor, change of detector response, etc. In chromatographic methods, the separation of the adjacent peaks is mandatory, and, consequently, the resolution is usually used as response. In isocratic elution methods, the resolution threshold depends on many factors, such as sizes of adjacent peaks, peak shapes, and asymmetry factor. At the same time, the situation is even more complex in gradient elution methods, because separation depends on a larger number of parameters, such as gradient profile, column geometry, mobile phase flow rate, column equilibration between gradient runs, etc. To ensure baseline separation, the authors propose application of separation criterion (s) as response and indirect modeling in the robustness evaluation. Examined response in this approach is represented by the difference between the retention time of the beginning of the peak and the retention time of the end of the previously eluting peak of the critical pair. Moreover, the proposed methodology included reusing experiments from the optimization phase to define a robust chromatographic region without increasing the number of experiments. It was shown that method robustness can be easily and efficiently evaluated by this methodology.
PB  - Springer Heidelberg, Heidelberg
T2  - Chromatographia
T1  - Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods
VL  - 81
IS  - 8
SP  - 1135
EP  - 1145
DO  - 10.1007/s10337-018-3545-x
ER  - 
@article{
author = "Sljivić, Jasmina and Protić, Ana and Malenović, Anđelija and Otašević, Biljana and Zečević, Mira",
year = "2018",
abstract = "In this paper, an efficient way for robustness testing of gradient elution liquid chromatographic methods is proposed and tested on model mixtures comprising cilazapril, hydrochlorothiazide, and their degradation products, solutes that differ not only in polarities, but also in solubility and absorption characteristics. In general, the robustness could be tested with respect to various responses: resolution, retention factor, selectivity factor, change of detector response, etc. In chromatographic methods, the separation of the adjacent peaks is mandatory, and, consequently, the resolution is usually used as response. In isocratic elution methods, the resolution threshold depends on many factors, such as sizes of adjacent peaks, peak shapes, and asymmetry factor. At the same time, the situation is even more complex in gradient elution methods, because separation depends on a larger number of parameters, such as gradient profile, column geometry, mobile phase flow rate, column equilibration between gradient runs, etc. To ensure baseline separation, the authors propose application of separation criterion (s) as response and indirect modeling in the robustness evaluation. Examined response in this approach is represented by the difference between the retention time of the beginning of the peak and the retention time of the end of the previously eluting peak of the critical pair. Moreover, the proposed methodology included reusing experiments from the optimization phase to define a robust chromatographic region without increasing the number of experiments. It was shown that method robustness can be easily and efficiently evaluated by this methodology.",
publisher = "Springer Heidelberg, Heidelberg",
journal = "Chromatographia",
title = "Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods",
volume = "81",
number = "8",
pages = "1135-1145",
doi = "10.1007/s10337-018-3545-x"
}
Sljivić, J., Protić, A., Malenović, A., Otašević, B.,& Zečević, M.. (2018). Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods. in Chromatographia
Springer Heidelberg, Heidelberg., 81(8), 1135-1145.
https://doi.org/10.1007/s10337-018-3545-x
Sljivić J, Protić A, Malenović A, Otašević B, Zečević M. Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods. in Chromatographia. 2018;81(8):1135-1145.
doi:10.1007/s10337-018-3545-x .
Sljivić, Jasmina, Protić, Ana, Malenović, Anđelija, Otašević, Biljana, Zečević, Mira, "Simple and Efficient Solution for Robustness Testing in Gradient Elution Liquid Chromatographic Methods" in Chromatographia, 81, no. 8 (2018):1135-1145,
https://doi.org/10.1007/s10337-018-3545-x . .
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Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide

Sljivić, Jasmina; Protić, Ana; Otašević, Biljana; Golubović, Jelena; Zečević, Mira; Krmar, Jovana

(Oxford Univ Press Inc, Cary, 2017)

TY  - JOUR
AU  - Sljivić, Jasmina
AU  - Protić, Ana
AU  - Otašević, Biljana
AU  - Golubović, Jelena
AU  - Zečević, Mira
AU  - Krmar, Jovana
PY  - 2017
UR  - https://farfar.pharmacy.bg.ac.rs/handle/123456789/2905
AB  - Multicriteria optimization methodology was applied in development of UHPLC-UV-MS method for separation of cilazapril, hydrochlorothiazide and their degradation products. This method is also applicable for analysis of cilazapril, hydrochlorothiazide and their degradation products in combined tablet formulation. Prior to method optimization forced degradation studies were conducted. Cilazapril and hydrochlorothiazide were subjected to acidic (0.1, 0.5 and 1.0M HCl), basic (0.1, 0.5 and 1.0M NaOH), thermal (70 degrees C), oxidative (3-30% H2O2) degradation and photodegradation (day light). Cilazapril appeared to be unstable toward acid and base and resulted in formation of cilazaprilat. Hydrochlorothiazide significantly degraded after acid, base and thermal hydrolysis and formed degradation product was 4-amino-6-chlorobenzene-1.3-disulfonamide. For both substances, after oxidative degradation unknown products have arisen. Initial percentage of acetonitrile in mobile phase, final percentage of acetonitrile in mobile phase, time of gradient elution and column temperature were defined as variables to be optimized toward two chromatographic responses by means of central composite design and Derringer's desirability function. The satisfactory chromatographic analysis was achieved on Kinetex C18 (2.6 mu m, 50 x 2.1 mm) column with temperature set at 25 degrees C. The final mobile phase consisted of acetonitrile and 20mM ammonium formate buffer (pH adjusted to 8.5). The flow rate of the mobile phase was 400 mu L min(-1) and it was pumped in a gradient elution mode.
PB  - Oxford Univ Press Inc, Cary
T2  - Journal of Chromatographic Science
T1  - Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide
VL  - 55
IS  - 6
SP  - 625
EP  - 637
DO  - 10.1093/chromsci/bmx018
ER  - 
@article{
author = "Sljivić, Jasmina and Protić, Ana and Otašević, Biljana and Golubović, Jelena and Zečević, Mira and Krmar, Jovana",
year = "2017",
abstract = "Multicriteria optimization methodology was applied in development of UHPLC-UV-MS method for separation of cilazapril, hydrochlorothiazide and their degradation products. This method is also applicable for analysis of cilazapril, hydrochlorothiazide and their degradation products in combined tablet formulation. Prior to method optimization forced degradation studies were conducted. Cilazapril and hydrochlorothiazide were subjected to acidic (0.1, 0.5 and 1.0M HCl), basic (0.1, 0.5 and 1.0M NaOH), thermal (70 degrees C), oxidative (3-30% H2O2) degradation and photodegradation (day light). Cilazapril appeared to be unstable toward acid and base and resulted in formation of cilazaprilat. Hydrochlorothiazide significantly degraded after acid, base and thermal hydrolysis and formed degradation product was 4-amino-6-chlorobenzene-1.3-disulfonamide. For both substances, after oxidative degradation unknown products have arisen. Initial percentage of acetonitrile in mobile phase, final percentage of acetonitrile in mobile phase, time of gradient elution and column temperature were defined as variables to be optimized toward two chromatographic responses by means of central composite design and Derringer's desirability function. The satisfactory chromatographic analysis was achieved on Kinetex C18 (2.6 mu m, 50 x 2.1 mm) column with temperature set at 25 degrees C. The final mobile phase consisted of acetonitrile and 20mM ammonium formate buffer (pH adjusted to 8.5). The flow rate of the mobile phase was 400 mu L min(-1) and it was pumped in a gradient elution mode.",
publisher = "Oxford Univ Press Inc, Cary",
journal = "Journal of Chromatographic Science",
title = "Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide",
volume = "55",
number = "6",
pages = "625-637",
doi = "10.1093/chromsci/bmx018"
}
Sljivić, J., Protić, A., Otašević, B., Golubović, J., Zečević, M.,& Krmar, J.. (2017). Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide. in Journal of Chromatographic Science
Oxford Univ Press Inc, Cary., 55(6), 625-637.
https://doi.org/10.1093/chromsci/bmx018
Sljivić J, Protić A, Otašević B, Golubović J, Zečević M, Krmar J. Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide. in Journal of Chromatographic Science. 2017;55(6):625-637.
doi:10.1093/chromsci/bmx018 .
Sljivić, Jasmina, Protić, Ana, Otašević, Biljana, Golubović, Jelena, Zečević, Mira, Krmar, Jovana, "Multicriteria Optimization Methodology in Stability-Indicating Method Development of Cilazapril and Hydrochlorothiazide" in Journal of Chromatographic Science, 55, no. 6 (2017):625-637,
https://doi.org/10.1093/chromsci/bmx018 . .
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