Assessment of Liquid Chromatographic Method Robustness by Use of Plackett-Burman Design

被引:20
作者
Maskovic, M. [1 ]
Jancic-Stojanovic, B. [2 ]
Malenovic, A. [2 ]
Ivanovic, D. [2 ]
Medenica, M. [3 ]
机构
[1] Med & Med Devices Agcy Serbia, Belgrade, Serbia
[2] Inst Drug Anal, Fac Pharm, Belgrade, Serbia
[3] Inst Phys Chem, Fac Pharm, Belgrade, Serbia
关键词
Plackett-Burman design; robustness; system-suitability tests; perindopril tert-butylamine; impurities; liquid chromatography; CAPILLARY-ELECTROPHORESIS; SUPERSATURATED DESIGNS; METHOD VALIDATION; LC METHOD; PERINDOPRIL; TESTS; TABLETS; MALEATE; ASSAY;
D O I
10.1556/AChrom.22.2010.2.10
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Robustness testing is an important part of method validation. Many ideas on robustness testing can be found in the literature, but the most useful approach is application of experimental design. In the work discussed in this paper, Plackett-Burman design was used for robustness testing of an LC method. Robustness was assessed for a previously validated method developed for chromatographic analysis of perindopril tert-butylamine and its impurities. Eleven factors (seven real and four dummies) in twelve experiments were examined. Robustness was assessed by graphical (half-normal probability plots and Pareto charts) and statistical (t-test) methods. For estimation of the standard error of effect (necessary for t-test estimation) calculations based on negligible effects and Dong's algorithm were used at the significance levels alpha = 0.05 and alpha = 0.01. In this way the effect of the factors was completely defined and, furthermore, nonsignificant intervals for significant variables were calculated. Finally, on the basis of the worst-case situation, system-suitability tests were performed and acceptance limits for certain values were calculated.
引用
收藏
页码:281 / 296
页数:16
相关论文
共 18 条
  • [1] [Anonymous], 2008, EUR PHARM
  • [2] Comparison of Plackett-Burman and supersaturated designs in robustness testing
    Dejaegher, B.
    Dumarey, M.
    Capron, X.
    Bloomfield, M. S.
    Heyden, Y. Vander
    [J]. ANALYTICA CHIMICA ACTA, 2007, 595 (1-2) : 59 - 71
  • [3] Randomization tests to identify significant effects in experimental designs for robustness testing
    Dejaegher, B
    Capron, X
    Smeyers-Verbeke, J
    Vander Heyden, Y
    [J]. ANALYTICA CHIMICA ACTA, 2006, 564 (02) : 184 - 200
  • [4] Comparison of spectrophotometric and an LC method for the determination perindopril and indapamide in pharmaceutical formulations
    Erk, N
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2001, 26 (01) : 43 - 52
  • [6] Validation of a LC method for the analysis of zafirlukast in a pharmaceutical formulation
    Ficarra, R
    Ficarra, P
    Tommasini, S
    Melardi, S
    Calabrò, ML
    Furlanetto, S
    Semreen, M
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2000, 23 (01) : 169 - 174
  • [7] Comparative study of different approaches to the determination of robustness for a sensitive-stacking capillary electrophoresis method.: Estimation of system suitability test limits from the robustness test
    Galeano-Diaz, Teresa
    Acedo-Valenzuela, Maria-Isabel
    Mora-Diez, Nielene
    Silva-Rodriguez, Antonio
    [J]. ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 389 (02) : 541 - 553
  • [8] Gumieniczek A, 1998, CHEM ANAL-WARSAW, V43, P951
  • [9] Ruggedness testing of chromatographic methods: selection of factors and levels
    Heyden, YV
    Questier, F
    Massart, L
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 1998, 18 (1-2) : 43 - 56
  • [10] Robustness testing of a reversed-phase high-performance liquid chromatographic assay: comparison of fractional and asymmetrical factorial designs
    Hund, E
    Vander Heyden, Y
    Haustein, M
    Massart, DL
    Smeyers-Verbeke, J
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2000, 874 (02) : 167 - 185