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Characterization of minocycline powder micronized by a supercritical antisolvent (SAS) process
The effect of the supercritical antisolvent micronization (SAS) process in the minocycline was evaluated in terms of particles morphology and density of the obtained powder. The minocycline was precipitated in a continuous mode from an ethanol solution using supercritical carbon dioxide as antisolve...
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Published in: | The Journal of supercritical fluids 2008-08, Vol.46 (1), p.71-76 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effect of the supercritical antisolvent micronization (SAS) process in the minocycline was evaluated in terms of particles morphology and density of the obtained powder. The minocycline was precipitated in a continuous mode from an ethanol solution using supercritical carbon dioxide as antisolvent and particles with a mean diameter around 250
nm were obtained (at 40
°C; 130
bar; solution concentration of 10
mg
mL
−1; solution flow rate of 1
mL
min
−1 and antisolvent flow rate, measured at room temperature and atmospheric pressure, of 6.56
L
min
−1). Moreover, the Scanning Electron Microscopy (SEM) and the X-ray Diffraction (XRD) allowed the comparison between the crystalline initial state and the amorphous particles obtained after the supercritical micronization process.
The density of the minocycline was determined by gas picnometry, before and after the micronization process, and the obtained results showed that it passes from an initial density of 1.574 to 2.951
g
cm
−3 after the processing. The increase in density of the micronized powder is clearly in contrast with the idea that SAS micronization produces a powder lighter than the starting material. A discussion about the stability and solubility of the precipitated powder, also contributes to highlight the potential of this micronization technique to integrate the pharmaceutical processing and to develop new formulations of this biopharmaceutical. |
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ISSN: | 0896-8446 1872-8162 |
DOI: | 10.1016/j.supflu.2008.02.018 |