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Batch and continuous blending of particulate material studied by near-infrared spectroscopy

Martínez Heredia, Lizbeth Araceli. Batch and continuous blending of particulate material studied by near-infrared spectroscopy. 2013, PhD Thesis, University of Basel, Faculty of Science.

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Official URL: http://edoc.unibas.ch/diss/DissB_10431

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Abstract

Background: Pharmaceutical manufacturing is moving towards real-time release of the
products. This objective can only be achieved by clearly understanding the process and by
implementing suitable technologies for manufacturing and for process control. Near-infrared
(NIR) spectroscopy is one technology that has attracted lot of attention from the pharmaceutical
industry since it can analyze bulk solids without any pretreatment, therefore reducing or
eliminating wet chemistry analysis. NIR spectroscopy is a powerful tool for the monitoring unit
operations were bulk material is involved i.e. blending of powders.
Blending of powders is a complex and poorly understood unit operation. In the pharmaceutical
industry blending has been performed batchwise and controlled by thief sampling. Thief
sampling is an invasive process which is tedious and tends to introduce bias; therefore an
alternative sampling method was highly needed. Here is where NIR found a perfect match with
blend uniformity monitoring, thus NIR implementation offers several advantages: thief sampling
is avoided, the process is continuously monitored, detection of blend-end point, and fast
identification of process deviations.
NIR spectral data need to be correlated with the parameter of interest (physical or chemical).
These computations are done by multivariate data analysis (MVDA). MVDA and NIR are a
powerful combination for in-process control and their use has been promoted by the health
authorities through the Process Analytical technology (PAT) initiative by the FDA.
Purpose: This thesis is focused on the study of powder blending, which is an essential unit
operation for the manufacture of solid dosage forms. The aim was to develop two quantitative
methods for the monitoring of the active ingredient concentration. One method was developed
for blend uniformity monitoring of a batch mixing process, and a second method for a
continuous mixing process.
This study also tackles the relevance of the physical presentation of the powder on the final
blend quality, by studying the influence of the particle size and the effect of the previous
manufacturing steps on the NIR spectral data.
Methods: Particle size was studied by NIR in diffuse reflectance mode, using Kubelka-Munk
function and the transformation of reflectance of absorbance values, in order to focus the
analysis on the physical properties. Furthermore, an off-line NIR model was developed for the
quantification of the mean particle size. Segregation tendencies due to particle size
incompatibilities were studied.
Blend uniformity monitoring of a batch pharmaceutical mixing was achieved through a NIR off-
line calibration method, which was used for the in-line drug quantification of a production scale
mixing process.
NIR in diffuse reflectance mode was used in the study of a continuous blending system. The
effect of the process parameters, i.e. flow rate and stirring rate, was analyzed. Moreover, a NIR
method for the in-line drug quantification was developed.
NIR was implemented in a powder stream, in which the mass of powder measured by NIR was
estimated.
Results and discussion: Regarding particle size, incompatibilities due to different particle size
ranges between the formulation ingredients lead to severe segregation. Particle size and
cohesion determined the quality of the powder blend; slight cohesion and broader particle size
distribution improved the robustness of the final blend. NIR showed high sensitivity to particle
size variations, thus it was possible to develop a quantitative model for the mean particle size
determination with a prediction error of 16 micrometers.
Concerning batch mixing, an off-line calibration was generated for the quantification of two
active ingredients contained in the formulation. The prediction errors varied from 0.4 to 2.3%
m/m for each of the drugs respectively. Special emphasis was given on the proper wavelength
selection for the quantitative analysis in order to focus the analysis on the active ingredients
quantification.
In relation to continuous blending of particulate material, a quantitative NIR model was
developed for the in-line prediction of the active ingredient concentration. The NIR model was
tested under different process conditions of feeding rate and stirring rate. High stirring rates
produce higher scattering of the NIR predictions. This was directly associated with the
acceleration of the particles at the outlet of the blender affecting the dwell time of the particles
with the NIR probe. The NIR model showed to be robust to moderate feed rate increments;
however the NIR model under-predicted the drug concentration under moderate feed rate
reductions of 30 kg/h. Furthermore, the continuous blending phases were clearly identified by
principal component analysis, moving block of standard deviation, and relative standard
deviation, all of them giving consistent results.
NIR measurements in a powder stream involved the scanning of powder flowing in a chute. The
flow of bulk solids is a complex phenomenon in which powder moves at a certain velocity. The
motion of particles produces changes in the density and distribution of the voids. In this study,
the velocity of the powder sliding down an inclined chute was measured and used for the
estimation of the NIR measured mass. The mass observed during one NIR measurement was
estimated to be less than one tablet.
Conclusions: This study proved the feasibility of applying NIR spectroscopy for the blend
uniformity monitoring of batch and continuous powder mixing. Understanding the critical
parameters of powder mixing lead to a robust process and reliable analytical methods. NIR
proved to be a valuable and versatile analytical tool in the measurement of bulk solids.
Advisors:Huwyler, Jörg
Committee Members:Liesum, Lorenz and Leuenberger, Hans
Faculties and Departments:05 Faculty of Science > Departement Pharmazeutische Wissenschaften > Pharmazie > Pharmazeutische Technologie (Huwyler)
Item Type:Thesis
Thesis no:10431
Bibsysno:Link to catalogue
Number of Pages:191 S.
Language:English
Identification Number:
Last Modified:30 Jun 2016 10:53
Deposited On:23 Jul 2013 07:28

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