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A novel method for the production of crystalline micronised particles
- Source :
- International Journal of Pharmaceutics. 388:114-122
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- The aim of this study was to develop a method for converting an amorphous drug to a crystalline form to enhance its stability and inhalation performance. Spray-dried amorphous salbutamol sulphate powder was conditioned with supercritical carbon dioxide (scCO 2 ) modified with menthol. The effect of menthol concentration, pressure, temperature and time on the characteristics of the resulting salbutamol sulphate powder was investigated. Pure scCO 2 had no effect on the physical properties of amorphous salbutamol sulphate; however, scCO 2 modified with menthol at 150 bar and 50 °C was efficient in converting amorphous drug to crystalline form after 12 h of conditioning. The average particle size of powders decreased slightly after the conditioning process because of reducing agglomeration between particles by increasing surface roughness. Emitted dose measured by the fine particle fraction (FPF emitted ) of amorphous salbutamol sulphate was enhanced from 32% to 43% after conditioning with scCO 2 + menthol and its water uptake was significantly decreased. This study demonstrates the potential of scCO 2 + menthol for converting amorphous forms of powders to crystalline, while preserving the particle size.
- Subjects :
- Time Factors
Surface Properties
Chemistry, Pharmaceutical
Pharmaceutical Science
law.invention
chemistry.chemical_compound
Drug Delivery Systems
Drug Stability
law
Administration, Inhalation
Organic chemistry
Albuterol
Particle Size
Crystallization
Supercritical carbon dioxide
Chemistry
Temperature
Water
Adrenergic beta-Agonists
Carbon Dioxide
Supercritical fluid
Amorphous solid
Menthol
Chemical engineering
Particle
Particle size
Drug carrier
Subjects
Details
- ISSN :
- 03785173
- Volume :
- 388
- Database :
- OpenAIRE
- Journal :
- International Journal of Pharmaceutics
- Accession number :
- edsair.doi.dedup.....e21240240a5497bf96a9bd49402b8f74
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2009.12.047