Monitoring Blending of Pharmaceutical Powders with Multipoint NIR Spectroscopy

Blending of powders is a crucial step in the production of pharmaceutical solid dosage forms. The active pharmaceutical ingredient (API) is often a powder that is blended with other powders (excipients) in order to produce tablets. The blending efficiency is influenced by several external factors, such as the desired degree of homogeneity and the required blending time, which mainly depend on the properties of the blended materials and on the geometry of the blender. This experimental study investigates the mixing behavior of acetyl salicylic acid as an API and α-lactose monohydrate as an excipient for different filling orders and filling levels in a blender. A multiple near-infrared probe setup on a laboratory-scale blender is used to observe the powder composition quasi-simultaneously and in-line in up to six different positions of the blender. Partial least squares regression modeling was used for a quantitative analysis of the powder compositions in the different measurement positions. The end point for the investigated mixtures and measurement positions was determined via moving block standard deviation. Observing blending in different positions helped to detect good and poor mixing positions inside the blender that are affected by convective and diffusive mixing.

[1]  Gabriele Reich,et al.  Near-infrared spectroscopy and imaging: basic principles and pharmaceutical applications. , 2005, Advanced drug delivery reviews.

[2]  E Bertran,et al.  Monitoring powder blending in pharmaceutical processes by use of near infrared spectroscopy. , 2002, Talanta.

[3]  Holger Grohganz,et al.  Design of Experiments-Based Monitoring of Critical Quality Attributes for the Spray-Drying Process of Insulin by NIR Spectroscopy , 2012, AAPS PharmSciTech.

[4]  Harnby An engineering view of pharmaceutical powder mixing. , 2000, Pharmaceutical science & technology today.

[5]  Andreas S. L. Mendez,et al.  Evaluation of powder mixing operation during batch production: Application to operational qualification procedure in the pharmaceutical industry , 2010 .

[6]  Keiji Imai,et al.  Process analytical technology applied for end-point detection of pharmaceutical blending by combining two calibration-free methods: Simultaneously monitoring specific near-infrared peak intensity and moving block standard deviation , 2011 .

[7]  C. Liew,et al.  Calibration sampling paradox in near infrared spectroscopy: a case study of multi-component powder blend. , 2010, International journal of pharmaceutics.

[8]  Ariel R. Muliadi,et al.  Evaluation of Three Approaches for Real-Time Monitoring of Roller Compaction with Near-Infrared Spectroscopy , 2012, AAPS PharmSciTech.

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

[10]  Y. Roggo,et al.  A review of near infrared spectroscopy and chemometrics in pharmaceutical technologies. , 2007, Journal of pharmaceutical and biomedical analysis.

[11]  J. Drennen,et al.  Near-infrared spectroscopy and imaging for the monitoring of powder blend homogeneity. , 2001, Journal of pharmaceutical sciences.

[12]  S. Wold,et al.  PLS-regression: a basic tool of chemometrics , 2001 .

[13]  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.

[14]  Benjamin J. Glasser,et al.  The effect of mixer properties and fill level on granular flow in a bladed mixer , 2009 .

[15]  M. Ghadiri The Letter from the Editor , 2009 .

[16]  J. J. McCarthy,et al.  Controlling cohesive particle mixing and segregation. , 2003, Physical review letters.

[17]  J G Khinast,et al.  The effect of agitated drying on the morphology of L-threonine (needle-like) crystals. , 2004, International journal of pharmaceutics.

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

[19]  J. Bertrand,et al.  Powder mixing: Some practical rules applied to agitated systems , 1991 .

[20]  Richard Hogg,et al.  Mixing and Segregation in Powders: Evaluation, Mechanisms and Processes , 2009 .

[21]  Benjamin J. Glasser,et al.  Mixing characteristics of wet granular matter in a bladed mixer , 2010 .

[22]  P. K. Aldridge,et al.  On-line monitoring of powder blend homogeneity by near-infrared spectroscopy. , 1996, Analytical chemistry.

[23]  Aditya U. Vanarase,et al.  Real-time monitoring of drug concentration in a continuous powder mixing process using NIR spectroscopy , 2010 .

[24]  Benjamin J. Glasser,et al.  Impact of agitated drying on crystal morphology: KCl–water system , 2003 .

[25]  Fernando J. Muzzio,et al.  Quantitative characterization of mixing of dry powders in V‐blenders , 1998 .

[26]  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.

[27]  Benjamin J. Glasser,et al.  Discrete element simulation of free flowing grains in a four‐bladed mixer , 2009 .

[28]  Nora Anne Urbanetz,et al.  Continuous quantitative monitoring of powder mixing dynamics by near-infrared spectroscopy , 2011 .

[29]  C. Abrahamsson Time-Resolved Spectroscopy for Pharmaceutical Applications , 2005 .