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Laser diffraction particle sizing of cohesive lactose powders

✍ Scribed by Handoko Adi; Ian Larson; Peter Stewart


Book ID
104088634
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
661 KB
Volume
179
Category
Article
ISSN
0032-5910

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✦ Synopsis


The objective was to develop a suitable laser diffraction particle sizing method for cohesive lactose present either as agglomerates or adhered onto coarse lactose carriers. Micronised lactose (ML) was prepared by fluid energy milling. Particle size distributions (PSD) were determined by laser diffraction (Malvern Master Sizer S, U.K.). Ethanol, propan-2-ol, 1-butanol and isooctane were selected as dispersants. Sonication for 5 min caused de-agglomeration of agglomerates initially formed in ethanol, propan-2-ol, and 1-butanol; the volume mean diameter (VMD) of ML in ethanol, propan-2-ol, and 1-butanol was 2.9 ΞΌm, 2.8 ΞΌm and 2.5 ΞΌm, respectively. Coarse lactose (Foremost 95 (F95)) showed a mono-modal distribution in all dispersants with a VMD of 117 ΞΌm in propan-2-ol. The robustness of particle sizing of ML in each dispersant was determined over time. Propan-2-ol was the most suitable dispersant for ML, as the PSD (VMD of 2.8 Β± 0.3 ΞΌm) did not change over a 3 h period. In comparison, for ethanol, VMD of FL was stable only for 30 min, but then increased from 2.9 ΞΌm to 9.0 ΞΌm after 3 h. The particle size changes over time occurring in ethanol were related to dissolution of fine lactose and possible re-crystallisation with subsequent increased VMD. ML added to coarse lactose and existing as agglomerated particles or as particles adhered to the coarse lactose could be determined with the use of a carefully selected sonication time to minimise coarse lactose comminution.


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