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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机构:
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
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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.
机构:
Hanoi Univ Sci & Technol, Sch Mech Engn, 1 Dai Co Viet, Hanoi, VietnamHanoi Univ Sci & Technol, Sch Mech Engn, 1 Dai Co Viet, Hanoi, Vietnam
Xuan, Doan Thanh
Nguyen, Hue Minh Thi
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Hanoi Natl Univ Educ, Fac Chem, 136 Xuan Thuy St, Hanoi 100000, Vietnam
Hanoi Natl Univ Educ, Ctr Computat Sci, 136 Xuan Thuy St, Hanoi 100000, VietnamHanoi Univ Sci & Technol, Sch Mech Engn, 1 Dai Co Viet, Hanoi, Vietnam
Nguyen, Hue Minh Thi
Hoang, Vu Dang
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Hanoi Univ Pharm, Fac Analyt Chem & Drug Qual Control, 13-15 Le Thanh Tong, Hanoi, VietnamHanoi Univ Sci & Technol, Sch Mech Engn, 1 Dai Co Viet, Hanoi, Vietnam