Development of liquid chromatographic method for the analysis of dabigatran etexilate mesilate and its ten impurities supported by quality-by-design methodology
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作者:
Pantovic, Jasmina
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Hemofarm Stada Doo, Qual Control Dept, Vrsac, SerbiaHemofarm Stada Doo, Qual Control Dept, Vrsac, Serbia
Pantovic, Jasmina
[1
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Malenovic, Andelija
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Univ Belgrade, Fac Pharm, Dept Drug Anal, Belgrade, SerbiaHemofarm Stada Doo, Qual Control Dept, Vrsac, Serbia
Malenovic, Andelija
[2
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Vemic, Ana
[2
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Kostic, Nada
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Univ Belgrade, Fac Pharm, Dept Drug Anal, Belgrade, SerbiaHemofarm Stada Doo, Qual Control Dept, Vrsac, Serbia
Kostic, Nada
[2
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Medenica, Mirjana
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Univ Belgrade, Fac Pharm, Dept Phys Chem & Instrumental Methods, Belgrade, SerbiaHemofarm Stada Doo, Qual Control Dept, Vrsac, Serbia
Medenica, Mirjana
[3
]
机构:
[1] Hemofarm Stada Doo, Qual Control Dept, Vrsac, Serbia
[2] Univ Belgrade, Fac Pharm, Dept Drug Anal, Belgrade, Serbia
[3] Univ Belgrade, Fac Pharm, Dept Phys Chem & Instrumental Methods, Belgrade, Serbia
In this paper, the development of reversed-phase liquid chromatographic method for the analysis of dabigatran etexilate mesilate and its ten impurities supported by quality by design (QbD) approach is presented. The defined analytical target profile (ATP) was the efficient baseline separation and the accurate determination of the investigated analytes. The selected critical quality attributes (CQAs) were the separation criterions between the critical peak pairs because the mixture complexity imposed a gradient elution mode. The critical process parameters (CPPs) studied in this research were acetonitrile content at the beginning of gradient program, acetonitrile content at the end of gradient program and the gradient time. Plan of experiments was defined by Box-Behnken design. The experimental domains of the three selected factors x1 - content of the acetonitrile at the start of linear gradient, x2 - content of the acetonitrile at the end of linear gradient and x3 - gradient time (t(G)) were 110%, 30%], [48%, 60%] and [8 min, 15 min], respectively. In order to define the design space (DS) as a zone where the desired quality criteria is met providing also the quality assurance, Monte Carlo simulations were performed. The uniform error distribution equal to the calculated standard error was added to the model coefficient estimates. Monte Carlo simulation included 5000 iterations in each of 3969 defined grid points and the region having the probability pi >= 95% to achieve satisfactory values of all defined CQAs was computed. As a working point, following chromatographic conditions suited in the middle of the DS were chosen: 22% acetonitrile at the start of gradient program, 55.5% acetonitrile at the end of gradient program end and the gradient time of 11.5 min. The developed method was validated in order to prove its reliability. (C) 2015 Elsevier B.V. All rights reserved.
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Med & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, SerbiaMed & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, Serbia
Terzic, Jelena
Popovic, Igor
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Med & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, SerbiaMed & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, Serbia
Popovic, Igor
Stajic, Ana
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Univ Belgrade, Dept Drug Anal, Fac Pharm, Vojvode Stepe 450, Belgrade 11000, SerbiaMed & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, Serbia
Stajic, Ana
Tumpa, Anja
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Univ Belgrade, Dept Drug Anal, Fac Pharm, Vojvode Stepe 450, Belgrade 11000, SerbiaMed & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, Serbia
Tumpa, Anja
Jancic-Stojanovic, Biljana
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Univ Belgrade, Dept Drug Anal, Fac Pharm, Vojvode Stepe 450, Belgrade 11000, SerbiaMed & Med Devices Agcy Serbia, Vojvode Stepe 458, Belgrade 11000, Serbia
机构:
Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Manoel, Joanna Wittckind
Primieri, Gabriele Bordignon
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Primieri, Gabriele Bordignon
Bueno, Livia Maronesi
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Bueno, Livia Maronesi
Wingert, Nathalie Ribeiro
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Wingert, Nathalie Ribeiro
Volpato, Nadia Maria
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Volpato, Nadia Maria
Garcia, Cassia Virginia
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Garcia, Cassia Virginia
Schapoval, Elfrides Eva Scherman
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil
Schapoval, Elfrides Eva Scherman
Steppe, Martin
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Univ Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, BrazilUniv Estadual Rio Grande do Sul, Lab Pharmaceut Qual Control, Porto Alegre, RS, Brazil