Validation of a multipoint near-infrared spectroscopy method for in-line moisture content analysis during freeze-drying.

This study assessed the validity of a multipoint near-infrared (NIR) spectroscopy method for in-line moisture content analysis during a freeze-drying process. It is known that the moisture content affects the stability of a freeze-dried product and hence it is a major critical quality attribute. Therefore assessment of the validity of an analytical method for moisture content determination is vital to ensure the quality of the final product. An aqueous sucrose solution was used as the model formulation of the study. The NIR spectra were calibrated to the moisture content using partial least squares (PLS) regression with coulometric Karl Fischer (KF) titration as the reference method. Different spectral preprocessing methods were compared for the PLS models. A calibration model transfer protocol was established to enable the use of the method in the multipoint mode. The accuracy profile was used as a decision tool to determine the validity of the method. The final PLS model, in which NIR spectra were preprocessed with standard normal variate transformation (SNV), resulted in low root mean square error of prediction value of 0.04%-m/v, i.e. evidence of sufficient overall accuracy of the model. The validation results revealed that the accuracy of the model was acceptable within the moisture content range 0.16-0.70%-m/v that is specific for the latter stages of the freeze-drying process. In addition, the results demonstrated the method's reliable in-process performance and robustness. Thus, the multipoint NIR spectroscopy method was proved capable of providing in-line evaluation of moisture content and it is readily available for use in laboratory scale freeze-drying research and development.

[1]  Leonard Steinborn,et al.  International Organization for Standardization ISO/IEC 17025 General Requirements for the Competence of Testing and Calibration Laboratories , 2004 .

[2]  E. Rozet,et al.  Near infrared and Raman spectroscopy as Process Analytical Technology tools for the manufacturing of silicone-based drug reservoirs. , 2011, Analytica chimica acta.

[3]  T. De Beer,et al.  Near-infrared spectroscopy for in-line monitoring of protein unfolding and its interactions with lyoprotectants during freeze-drying. , 2012, Analytical chemistry.

[4]  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.

[5]  A. Sparén,et al.  In-Situ Near-Infrared Spectroscopy Monitoring of the Lyophilization Process , 2003, Pharmaceutical Research.

[6]  Max Feinberg,et al.  Validation of analytical methods based on accuracy profiles. , 2007, Journal of chromatography. A.

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

[8]  Sajal Manubhai Patel,et al.  Process Analytical Technologies (PAT) in freeze-drying of parenteral products , 2009, Pharmaceutical development and technology.

[9]  W. Luck,et al.  APPROXIMATE METHODS FOR DETERMINING THE STRUCTURE OF H$sub 2$O AND HOD USING NEAR-INFRARED SPECTROSCOPY. , 1970 .

[10]  Emil W. Ciurczak,et al.  Handbook of Near-Infrared Analysis , 1992 .

[11]  Patrice Chiap,et al.  Harmonization of strategies for the validation of quantitative analytical procedures , 2007 .

[12]  C Vervaet,et al.  In-line and real-time process monitoring of a freeze drying process using Raman and NIR spectroscopy as complementary process analytical technology (PAT) tools. , 2009, Journal of pharmaceutical sciences.

[13]  P. Hubert,et al.  Improvement of the decision efficiency of the accuracy profile by means of a desirability function for analytical methods validation. Application to a diacetyl-monoxime colorimetric assay used for the determination of urea in transdermal iontophoretic extracts. , 2007, Analytica chimica acta.

[14]  K. Järvinen,et al.  In-line multipoint near-infrared spectroscopy for moisture content quantification during freeze-drying. , 2013, Analytical chemistry.

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

[16]  C. Yomota,et al.  Near-infrared analysis of protein secondary structure in aqueous solutions and freeze-dried solids. , 2006, Journal of pharmaceutical sciences.

[17]  P. Eilers A perfect smoother. , 2003, Analytical chemistry.

[18]  M Laurentie,et al.  Harmonization of strategies for the validation of quantitative analytical procedures: a SFSTP proposal part IV. Examples of application. , 2008, Journal of pharmaceutical and biomedical analysis.

[19]  J. Mantanus,et al.  Moisture content determination of pharmaceutical pellets by near infrared spectroscopy: method development and validation. , 2009, Analytica chimica acta.

[20]  R. Barnes,et al.  Standard Normal Variate Transformation and De-Trending of Near-Infrared Diffuse Reflectance Spectra , 1989 .

[21]  P Sheehan,et al.  Modeling of the primary and secondary drying stages of the freeze drying of pharmaceutical products in vials: numerical results obtained from the solution of a dynamic and spatially multi-dimensional lyophilization model for different operational policies. , 1998, Biotechnology and bioengineering.

[22]  Jérôme Mantanus,et al.  Building the quality into pellet manufacturing environment--feasibility study and validation of an in-line quantitative near infrared (NIR) method. , 2010, Talanta.

[23]  P. Hubert,et al.  Using tolerance intervals in pre-study validation of analytical methods to predict in-study results. The fit-for-future-purpose concept. , 2007, Journal of chromatography. A.

[24]  Tormod Næs,et al.  A user-friendly guide to multivariate calibration and classification , 2002 .

[25]  J. Fricke,et al.  Effective Sample Size in Diffuse Reflectance Near-IR Spectrometry. , 1999, Analytical chemistry.

[26]  Chung C. Hsu,et al.  Effect of Moisture on the Stability of a Lyophilized Humanized Monoclonal Antibody Formulation , 2001, Pharmaceutical Research.

[27]  Robert Cogdill,et al.  Near-Infrared Spectroscopy , 2006 .

[28]  Michael J Pikal,et al.  Effect of sorbitol and residual moisture on the stability of lyophilized antibodies: Implications for the mechanism of protein stabilization in the solid state. , 2005, Journal of pharmaceutical sciences.

[29]  J. Mantanus,et al.  Acetaminophen determination in low-dose pharmaceutical syrup by NIR spectroscopy. , 2010, Journal of pharmaceutical and biomedical analysis.

[30]  M. Manning,et al.  Noninvasive determination of protein conformation in the solid state using near infrared (NIR) spectroscopy. , 2005, Journal of pharmaceutical sciences.

[31]  T. Fearn Standardisation and Calibration Transfer for near Infrared Instruments: A Review , 2001 .

[32]  C Vervaet,et al.  Near infrared and Raman spectroscopy for the in-process monitoring of pharmaceutical production processes. , 2011, International journal of pharmaceutics.

[33]  L Delattre,et al.  Validation of manufacturing process of Diltiazem HCl tablets by NIR spectrophotometry (NIRS). , 2007, Journal of pharmaceutical and biomedical analysis.

[34]  T. De Beer,et al.  Optimization of a pharmaceutical freeze-dried product and its process using an experimental design approach and innovative process analyzers. , 2011, Talanta.

[35]  C. De Bleye,et al.  Critical review of near-infrared spectroscopic methods validations in pharmaceutical applications. , 2012, Journal of pharmaceutical and biomedical analysis.