Acta Pharmaceutica, Vol. 62 No. 1, 2012.
Review article
https://doi.org/10.2478/v10007-012-0010-5
Spherical crystallization of drugs
BORUT KOVAČIČ
; Krka d. d., 8501 Novo mesto, Slovenia; University of Ljubljana, Faculty of Pharmacy, 1000 Ljubljana, Slovenia
FRANC VREČER
; Krka d. d., 8501 Novo mesto, Slovenia; University of Ljubljana, Faculty of Pharmacy, 1000 Ljubljana, Slovenia
ODON PLANINŠEK
; University of Ljubljana, Faculty of Pharmacy, Aškerčeva 7, 1000 Ljubljana, Slovenia
Abstract
Spherical crystallization of drugs is the process of obtaining larger particles by agglomeration during crystallization. The most common techniques used to obtain such particles are spherical agglomeration and quasi-emulsion solvent diffusion. Ammonia diffusion systems and crystallo-co-agglomeration are extensions of these techniques. By controlling process parameters during crystallization, such as temperature, stirring rate, type and amount of solvents, or excipient selection, it is possible to control the formation of agglomerates and obtain spherical particles of the desired size, porosity, or hardness. Researchers have reported that the particles produced have improved micromeritic, physical, and mechanical properties, which make them suitable for direct compression. In some cases, when additional excipients are incorporated during spherical crystallization, biopharmaceutical parameters including the bioavailability of drugs can also be tailored.
Keywords
spherical crystallization; agglomeration; solvent diffusion; improved particle properties
Hrčak ID:
76606
URI
Publication date:
31.3.2012.
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