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EN
Fluidized-bed spray granulation (FBSG) enables manufacturing particles with desired characteristics, including particle size distribution (PSD), density, or dust content. This study investigated the effect of selected factors on the granules obtained in a continuous FBSG of chelated fertilizers for foliar applications. The effect of surfactant addition to the solution sprayed into the bed and perturbations of operating parameters on PSD and granules morphology was studied. The experiments were supplemented with calculations based on a population balance equation (PBE). It was shown that granules manufactured with the tenside addition are more regular in shape, and thus less prone to mechanical wear. It was demonstrated that increasing rotational mill speed does contribute to a slight increase in the amount of dust, but in the long term, it does not disturb the regular agglomeration process. The computational results confirm that, despite the complexity of the process, its description with PBE is feasible.
EN
Rab3D is a low molecular weight GTP-binding protein that associates with secretory granules in exocrine cells. AR42J cells are derived from rat pancreatic exocrine tumor cells and develop an acinar cell-like phenotype when treated with dexamethasone (Dex). In the present study, we examined the role of Rab3D in Dex-treated AR42J cells. Rab3D expression and localization were analyzed by subcellular fractionation and immunoblotting. The role of Rab3D was examined by overexpressing myc-labeled wild-type-Rab3D and a constitutively active form of Rab3D (Rab3D-Q81L) in AR42J cells. We found that Rab3D is predominantly membrane-associated in AR42J cells and co-localizes with zymogen granules (ZG). Following CCK-8-induced exocytosis, amylase-positive ZGs appeared to move towards the periphery of the cell and co-localization between Rab3D and amylase was less complete when compared to basal conditions. Overexpression of WT, but not mutant Rab3D, resulted in an increase in cellular amylase levels. Overexpression of mutant and WT Rab3D did not affect granule morphology, CCK-8-induced secretion, long-term (48 hr) basal amylase release or granule density. We conclude that Rab3D is not involved in agonist-induced exocytosis in AR42J cells. Instead, Rab3D may regulate amylase content in these cells.
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