Moisture and drug solid-state monitoring during a continuous drying process using empirical and mass balance models
Pyrrolidines
Spectroscopy, Near-Infrared
Chemistry, Pharmaceutical
Temperature
Humidity
Lactose
02 engineering and technology
Spectrum Analysis, Raman
Molecular Weight
Pharmaceutical Preparations
Theophylline
Calibration
Technology, Pharmaceutical
Polyvinyls
Powders
0210 nano-technology
Tablets
DOI:
10.1016/j.ejpb.2014.02.015
Publication Date:
2014-03-06T09:31:49Z
AUTHORS (10)
ABSTRACT
Classically, the end point detection during fluid bed drying has been performed using indirect parameters, such as the product temperature or the humidity of the outlet drying air. This paper aims at comparing those classic methods to both in-line moisture and solid-state determination by means of Process Analytical Technology (PAT) tools (Raman and NIR spectroscopy) and a mass balance approach. The six-segmented fluid bed drying system being part of a fully continuous from-powder-to-tablet production line (ConsiGma™-25) was used for this study. A theophylline:lactose:PVP (30:67.5:2.5) blend was chosen as model formulation. For the development of the NIR-based moisture determination model, 15 calibration experiments in the fluid bed dryer were performed. Six test experiments were conducted afterwards, and the product was monitored in-line with NIR and Raman spectroscopy during drying. The results (drying endpoint and residual moisture) obtained via the NIR-based moisture determination model, the classical approach by means of indirect parameters and the mass balance model were then compared. Our conclusion is that the PAT-based method is most suited for use in a production set-up. Secondly, the different size fractions of the dried granules obtained during different experiments (fines, yield and oversized granules) were compared separately, revealing differences in both solid state of theophylline and moisture content between the different granule size fractions.
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