Calibration sampling paradox in near infrared spectroscopy: a case study of multi-component powder blend.

The objective of this study was to illustrate the sampling paradox resulting from the different strategies of spectral acquisition while preparing and implementing the calibration models for prediction of blend components in multi-component cohesive blends. A D-optimal mixture design was used to create 24 blending runs of the formulation consisting of chlorpheniramine maleate, lactose, microcrystalline cellulose and magnesium stearate. Three strategies: (a) laboratory mixing and static spectral acquisition, (b) IBC mixing and static spectral acquisition and (c) IBC mixing and dynamic spectral acquisition were investigated for obtaining the most relevant and representative calibration samples. An optical head comprising a sapphire window mounted on the lid of the IBC was used for static and dynamic NIR spectral acquisition of the powder blends. For laboratory mixed samples, powders were blended for fixed period of 30 min and later on scanned for NIR spectra. For IBC mixed blends, the spectral acquisition was carried out in-line for 2 min and stopped for static spectral acquisition. The same cycle was repeated for the next 28 min. Partial least square (PLS) calibration models for each component were built and ranked according to their calibration statistics. Optimal calibration models were selected from each strategy for each component and used for in-line prediction of blend components of three independent test runs. Although excellent statistics were obtained for the PLS models from the three strategies, significant discrepancies were observed during prediction of the independent blends in real time. Models built using IBC mixed blends and dynamic spectral acquisition resulted in the most accurate predictions for all the blend components, whereas models prepared using static spectral acquisition (laboratory mixed and IBC) showed erroneous prediction results. The prediction performance differences between the models obtained using the different strategies could be explained in the context of relevancy and representative sample collection at the initial stage of calibration model building.

[1]  Rodolfo J. Romañach,et al.  Blend uniformity analysis using stream sampling and near infrared spectroscopy , 2002, AAPS PharmSciTech.

[2]  Paulo E Arratia,et al.  Mixing of Cohesive Pharmaceutical Formulations in Tote (Bin) Blenders , 2002, Drug development and industrial pharmacy.

[3]  Fernando Muzzio,et al.  A Homogeneity Study Using NIR Spectroscopy: Tracking Magnesium Stearate in Bohle Bin-Blender , 2003, Drug development and industrial pharmacy.

[4]  Huiquan Wu,et al.  Quality-by-design (QbD): an integrated multivariate approach for the component quantification in powder blends. , 2009, International journal of pharmaceutics.

[5]  Zhenqi Shi,et al.  Process characterization of powder blending by near-infrared spectroscopy: blend end-points and beyond. , 2008, Journal of pharmaceutical and biomedical analysis.

[6]  C. Ufret,et al.  Modeling of Powder Blending Using On-line Near-Infrared Measurements , 2001, Drug development and industrial pharmacy.

[7]  J. Drennen,et al.  A Process Analytical Technology approach to near-infrared process control of pharmaceutical powder blending. Part III: Quantitative near-infrared calibration for prediction of blend homogeneity and characterization of powder mixing kinetics. , 2006, Journal of pharmaceutical sciences.

[8]  Abhay Gupta,et al.  Real-time on-line blend uniformity monitoring using near-infrared reflectance spectrometry: a noninvasive off-line calibration approach. , 2009, Journal of pharmaceutical and biomedical analysis.

[9]  Charles E. Miller,et al.  Chemometrics in Process Analytical Chemistry , 2007 .

[10]  C. Liew,et al.  In-line quantification of drug and excipients in cohesive powder blends by near infrared spectroscopy. , 2010, International journal of pharmaceutics.

[11]  L. Danielsson,et al.  Quantitative in-line monitoring of powder blending by near infrared reflection spectroscopy , 2002 .

[12]  L. Cartilier,et al.  Cohesive, multicomponent, dense powder flow characterization by NIR. , 2007, International journal of pharmaceutics.

[13]  Weiyong. Li,et al.  Quantitation of active pharmaceutical ingredients and excipients in powder blends using designed multivariate calibration models by near-infrared spectroscopy. , 2005, International journal of pharmaceutics.

[14]  David Littlejohn,et al.  Effects of particle size and cohesive properties on mixing studied by non-contact NIR. , 2008, International journal of pharmaceutics.

[15]  Weiyong. Li,et al.  Mass-balanced blend uniformity analysis of pharmaceutical powders by at-line near-infrared spectroscopy with a fiber-optic probe. , 2006, International journal of pharmaceutics.