Supercritical fluid assisted atomization introduced by hydrodynamic cavitation mixer for micronization of roxithromycin
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Supercritical fluid assisted atomization introduced by hydrodynamic cavitation mixer for micronization of roxithromycin
CIESC JournalIssue 2, Pages: 293-300(2008)
作者机构:
浙江大学化学工程与生物工程学系
作者简介:
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DOI:
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Online First:05 February 2008,
Published:05 February 2008
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CAI Meiqiang, GUAN Yixin, YAO Shanjing, et al. Supercritical fluid assisted atomization introduced by hydrodynamic cavitation mixer for micronization of roxithromycin[J]. CIESC Journal, 2008, (2): 293-300.
DOI:
CAI Meiqiang, GUAN Yixin, YAO Shanjing, et al. Supercritical fluid assisted atomization introduced by hydrodynamic cavitation mixer for micronization of roxithromycin[J]. CIESC Journal, 2008, (2): 293-300.DOI:
Supercritical fluid assisted atomization introduced by hydrodynamic cavitation mixer for micronization of roxithromycin
Based upon the mechanism of supercritical fluid assisted atomization (SAA) technology
a promising process for producing micronic particles of controlled diameter
it was proposed that the mixing between supercritical CO2 and liquid solution in the saturator was one of the key factors likely responsible for the particle size distribution (PSD) width.The SAA introduced by hydrodynamic cavitation mixer (SAA-HCM) experimental apparatus was built to intensify mass transfer and form a homogeneous fluid mixture.Using roxithromycin as the model drug
the effects of process parameters
such as cavitation generator
mixer pressure
precipitator temperature
different solvents
mass flow ratio between CO2 and liquid solution and solute concentration in the liquid solution were investigated to evaluate their influences on the morphology and size of precipitated particles.The results indicated that hydrodynamic cavitation mixer improved effectively mass transfer
and successful micronization of the roxithromycin was achieved with a narrow PSD.Most of the particles obtained by using the SAA-HCM were well-defined spherical in morphology.By adjusting process parameters
microparticles with a diameter ranging between 1μm and 3μm suitable for inhalation delivery and ultrafine microparticles with a diameter lower than 1μm could be obtained.