## Abstract ## Background Dry powder dispersion devices offer potential for delivering therapeutic macromolecules to the pulmonary epithelia. Previously, freezeβdrying (lyophilisation) has been the accepted method for preparing dried formulations of proteins and nonβviral gene vectors despite the
Preparation of kanamycin powder by an optimized spray freeze-drying method
β Scribed by Jae-Young Her; Chi-Sung Song; Seung Ju Lee; Kwang-Geun Lee
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 731 KB
- Volume
- 199
- Category
- Article
- ISSN
- 0032-5910
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β¦ Synopsis
The physical and antibiotic properties of kanamycin powders obtained by spray freeze drying (SFD) were compared with those of raw kanamycin. The SFD procedures were optimized to prepare kanamycin for use as an inhaled drug. Scanning electron microscopy (SEM) and a laser particle size analyzer were applied to estimate physical structure and properties of the particle. In addition, the disk diffusion method was used to compare the antibiotic activity of raw kanamycin and that produced by SFD. According to SEM, the kanamycin particles had various sizes and shapes with porous structures at different SFD conditions. The diameters of the kanamycin powders were between 13.5 ΞΌm and 21.8 ΞΌm, and their aerodynamic particle sizes were between 3.58 ΞΌm and 6.39 ΞΌm. The antibiotic activities of the raw and spray freeze-dried kanamycin samples were not significantly different (P N 0.05). The optimized conditions for annealing temperature, annealing time, kanamycin concentration, pressure, and nozzle tip lift were -15 Β°C, 5 h, 10% kanamycin, 100 kPa, and, 1 mm, respectively.
π SIMILAR VOLUMES
Ultrafine cobalt powders have been prepared by the freeze-drying method and supported cobalt catalysts have been prepared by a new freeze-drying immersion method. The results of XRD and SEM showed that the precursors were amorphous and most were massive with a size range of 2-5 Β΅m. In the cobalt pow