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Frantisek Stepanek

Publications and source records attributed to Frantisek Stepanek.

2 recordsLinked to original sources

Formation of hollow core granules by fluid bed in situ melt granulation: modelling and experiments.

Granules with a characteristic core-shell internal structure have been formed by in situ melt fluid-bed granulation, using d-mannitol primary solid particles and poly-ethylene glycol (PEG-6000) binder. The effect of binder particle size and binder/solids ratio on granule size distribution was systematically investigated. The mean granule size was found to be directly proportional to the binder particle size. The binder amount did not measurably affect the granule size, only the fraction of un-granulated fines. The microstructure of the granules was analysed by X-ray micro-tomography; the average shell thickness in the granules was found to depend on the binder/solids ratio, and the core volume was found to be directly proportional to the binder particle size. However, for binder particle size below a certain value the core-shell structure disappeared. A mathematical model based on a layering growth mechanism has been proposed and found to be consistent with experimental data. The proposed growth mechanism was confirmed by creating granules with bi-modal size distribution using a mixture of differently sized binder seeds.

Particle Size↗

Multiscale modelling methodology for virtual prototyping of effervescent tablets.

Computational methodology for virtual tablet prototyping has been developed. The methodology consists of two steps: construction of virtual particle compacts of varying composition using the discrete element method (DEM), and the simulation of their dissolution by eroding individual components from the tablet microstructure according to their intrinsic dissolution rates, using the volume-of-fluid (VOF) method. The effective erosion rate obtained from simulations at the particle assembly length-scale is used for the calculation of dissolution time at the tablet length-scale. The methodology is demonstrated on the case of a simple effervescent formulation consisting of sodium bicarbonate-acetic acid effervescent system, sodium chloride as a model active substance, and lactose filler. The experimentally measured dependence of tablet dissolution time on composition and compaction force was found to be in very good agreement with outputs from computer simulations.

Citric Acid↗