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Mechanistic modeling of semicontinuous fluidized bed drying of pharmaceutical granules by incorporating single particle and bulk drying kinetics.
Vandeputte, Tuur; Ghijs, Michael; Van Hauwermeiren, Daan; Dos Santos Schultz, Eduardo; Schäfer, Elisabeth; Stauffer, Fanny; De Beer, Thomas; Nopens, Ingmar.
Afiliação
  • Vandeputte T; BIOMATH, Department of Data Analysis and Mathematical Modelling, Ghent University, B-9000 Ghent, Belgium; Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, B-9000 Ghent, Belgium.
  • Ghijs M; BIOMATH, Department of Data Analysis and Mathematical Modelling, Ghent University, B-9000 Ghent, Belgium; Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, B-9000 Ghent, Belgium.
  • Van Hauwermeiren D; BIOMATH, Department of Data Analysis and Mathematical Modelling, Ghent University, B-9000 Ghent, Belgium; Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, B-9000 Ghent, Belgium.
  • Dos Santos Schultz E; Discovery, Product Development & Supply, Janssen R&D, B-2340 Beerse, Belgium.
  • Schäfer E; Discovery, Product Development & Supply, Janssen R&D, B-2340 Beerse, Belgium.
  • Stauffer F; UCB Pharma S.A, B-1420 Braine-l'Alleud, Belgium.
  • De Beer T; Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, B-9000 Ghent, Belgium. Electronic address: Thomas.DeBeer@Ugent.be.
  • Nopens I; BIOMATH, Department of Data Analysis and Mathematical Modelling, Ghent University, B-9000 Ghent, Belgium.
Int J Pharm ; 646: 123447, 2023 Nov 05.
Article em En | MEDLINE | ID: mdl-37770009
ABSTRACT
In this work, a mechanistic fluidized bed drying model computing the granule moisture content in function of granule size, drying time, process settings and formulation properties is developed. Modeling the moisture content distribution concerning the granule size is essential for tabletability and drug product quality. This work combines a mechanistic bulk model and a single-particle drying kinetics model in a semicontinuous mode. The added model complexity allows physical approximations of drying phenomena at both the drying system level and the granular level. This includes quantifying the variations in moisture content by taking into account the specific dryer design and the variations in granule size. The model performance was quantified through industrially relevant case studies. It was revealed that the proposed model structure accurately predicts the drying behavior of the yield fraction. However, systematic model biases were observed for the fine and coarse fractions of the granule size distribution. In addition, discrepancies in the predicted outgoing air properties (relative air humidity and air temperature) were obtained. Further enhancement of the model complexity, e.g. complete incorporation of fluidization and segregation phenomena, is likely to improve the model performance. Notwithstanding, the developed model forms a step towards a formulation-generic fluidized bed drying model as interacting mechanisms on different levels of the drying system are considered.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Pharm Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Int J Pharm Ano de publicação: 2023 Tipo de documento: Article