Procedure for the Selection and Validation of a Calibration Model II-Theoretical Basis.

In the first part of this paper (I-Description and application), an automated, stepwise and analyst-independent process for the selection and validation of calibration models was put forward and applied to two model analytes. This second part presents the mathematical reasoning and experimental work underlying the selection of the different components of this procedure. Different replicate analysis designs (intra/inter-day and intra/inter-extraction) were tested and their impact on test results was evaluated. For most methods, the use of intra-day/intra-extraction measurement replicates is recommended due to its decreased variability. This process should be repeated three times during the validation process in order to assess the time stability of the underlying model. Strategies for identification of heteroscedasticity and their potential weaknesses were examined and a unilateral F-test using the lower limit of quantification and upper limit of quantification replicates was chosen. Three different options for model selection were examined and tested: ANOVA lack-of-fit (LOF), partial F-test and significance of the second-order term. Examination of mathematical assumptions for each test and LC-MS-MS experimental results lead to selection of the partial F-test as being the most suitable. The advantages and drawbacks of ANOVA-LOF, examination of the standardized residuals graph and residuals normality testing (Kolmogorov-Smirnov or Cramer-Von Mises) for validation of the calibration model were examined with the last option proving the best in light of its robustness and accuracy. Choosing the correct calibration model improves QC accuracy, and simulations have shown that this automated scheme has a much better performance than a more traditional method of fitting with increasingly complex models until QC accuracies pass below a threshold.

[1]  Y. L. Loukas,et al.  Development and validation of an improved high-throughput method for the determination of anastrozole in human plasma by LC-MS/MS and atmospheric pressure chemical ionization. , 2008, Journal of pharmaceutical and biomedical analysis.

[2]  Z. Mester,et al.  Calibration graphs in isotope dilution mass spectrometry. , 2015, Analytica chimica acta.

[3]  M Laurentie,et al.  Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part II. , 2004, Journal of pharmaceutical and biomedical analysis.

[4]  A. Polettini Applications of LC-MS in Toxicology , 2006 .

[5]  Helmut Gnnzler,et al.  Validation in Chemical Measurement , 2005 .

[6]  Olaf H Drummer,et al.  Validation of new methods. , 2007, Forensic science international.

[7]  D. Darling The Kolmogorov-Smirnov, Cramer-von Mises Tests , 1957 .

[8]  L. Nilsson,et al.  Direct quantification in bioanalytical LC-MS/MS using internal calibration via analyte/stable isotope ratio. , 2007, Journal of pharmaceutical and biomedical analysis.

[9]  D L Massart,et al.  Validation of bioanalytical chromatographic methods. , 1998, Journal of pharmaceutical and biomedical analysis.

[10]  Vinod P. Shah,et al.  Validation of Bioanalytical Methods , 1991, Pharmaceutical Research.

[11]  Validation of the calibration procedure in atomic absorption spectrometric methods , 1996 .

[12]  Jon A. Wellner,et al.  Empirical processes indexed by estimated functions , 2007, 0709.1013.

[13]  Huidong Gu,et al.  Selecting the correct weighting factors for linear and quadratic calibration curves with least-squares regression algorithm in bioanalytical LC-MS/MS assays and impacts of using incorrect weighting factors on curve stability, data quality, and assay performance. , 2014, Analytical chemistry.

[14]  Y. Michotte,et al.  Use of microbore LC-MS/MS for the quantification of oxcarbazepine and its active metabolite in rat brain microdialysis samples. , 2006, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[15]  S. Weisberg,et al.  Residuals and Influence in Regression , 1982 .

[16]  Jon A. Wellner,et al.  Weak Convergence and Empirical Processes: With Applications to Statistics , 1996 .

[17]  C. Skinner,et al.  Determination of confidence intervals in non-normal data: application of the bootstrap to cocaine concentration in femoral blood. , 2015, Journal of analytical toxicology.

[18]  Jim X Shen,et al.  Reasons for calibration standard curve slope variation in LC-MS assays and how to address it. , 2014, Bioanalysis.

[19]  Eric Ziemons,et al.  Analysis of recent pharmaceutical regulatory documents on analytical method validation. , 2007, Journal of chromatography. A.

[20]  Vinod P. Shah,et al.  Bioanalytical Method Validation—A Revisit with a Decade of Progress , 2000, Pharmaceutical Research.

[21]  J. Miller,et al.  Statistics and chemometrics for analytical chemistry , 2005 .

[22]  G T Barnes,et al.  Signal-to-noise ratio considerations in radiographic imaging. , 1983, Medical physics.

[23]  Philippe Hubert,et al.  The SFSTP guide on the validation of chromatographic methods for drug bioanalysis: from the Washington Conference to the laboratory , 1999 .

[24]  Johanna Smeyers-Verbeke,et al.  Handbook of Chemometrics and Qualimetrics: Part A , 1997 .

[25]  A. Gustavo González,et al.  A practical guide to analytical method validation, including measurement uncertainty and accuracy profiles , 2007 .

[26]  D. Hillaire‐buys,et al.  Application of a standardized coextractive cleanup procedure to routine high-performance liquid chromatography assays of teicoplanin and ganciclovir in plasma. , 1998, Journal of Chromatography B: Biomedical Sciences and Applications.

[27]  S. Rana,et al.  Determination of meperidine, tramadol and oxycodone in human oral fluid using solid phase extraction and gas chromatography-mass spectrometry. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[28]  Eric R. Ziegel,et al.  Statistics and Chemometrics for Analytical Chemistry , 2004, Technometrics.

[29]  J. Burrows,et al.  Linearity of chromatographic systems in drug analysis part I: theory of nonlinearity and quantification of curvature. , 2015, Bioanalysis.