Feature: for medium temperatures > °C or frequent changes in temperature. 0 to 1 bar – 0 to 60 bar relative, 0 to 1 bar – 0 to 25 bar absolute; Medium. HART® interface; Optional explosion protection [Ex ia] according to ATEX, GOST- R, DNV; Linearity %; Turn down: ; Simple operation with rotary knob. Get this from a library! Farmacevtska tehnologija. Del 1, Praktikum. [Julijana Kristl ; Jelka Šmid-Korbar; Stanko Srčič].
Solid state analysis confirmed unaltered physical state of the granulate components and the farmacevtsia interactions between the active and excipients.
Farmacevtska tehnologija: za studii i praktika – Angel Simov – Google Books
Binder content was shown to be important for narrow size distribution tebnologija goodflow properties. URL – Presentation file, Visit http: Voting is allowed only to logged in users.
You have to log in to leave a comment. You have to log in to leave a comment. CFD simulations were performed in a 2D tehnologijx space using the two-fluid model. Computational fluid dynamics CFD simulations and experimental measurements of laboratory-scale Wurster coating were performed. The effect of the Wurster gap and fluidizing air flow rate on gas-solidflow was analyzed in both simulations and experiments.
The results of the present study farmaceftska that fluidized hot melt granulation is a promising powder agglomeration technique for spherical granules production.
The results obtained indicate that teunologija fluid bedgranulator may be suitable for production of highly spherical agglomerates,particularly when immersion and layering is dominant agglomeration mechanism.
Pellet coating is commonly performed in a fluid bed coater such as a Wurster coater. A rather good agreement between the simulated and experimental results was observed and thus it can be assumeed that this particular simulation setup represents a computationally reasonable tool that provides a valuable insight into the Wurster coating process due to the impact of two-phase flow properties on the process.
Granule size was mainly influenced by binder particle size. The aim of this study was to investigate the influence of binder content, binder particle size, granulation time and inlet air flow rate on granule sizeand size distribution, granule shape and flowability, as well as on drug release rate. Hydrophilic polyetilenglycol and hydrophobic meltable binder glyceryl palmitostearate were used for in situ fluidized hot melt granulation.