Simultaneous particulate design of primary and agglomerated crystals of steroid by spherical agglomeration in liquid for dry powder inhalation

Spherical agglomerates of steroid KSR-592, consisting of fine primary drug crystals suitable for dry powder inhalation (DPI), were prepared by the spherical agglomeration method in liquid with a bridging liquid. It was found that the particle size of primary crystals increased until the dispersing medium was saturated with the bridging liquid, whereas the spherical agglomeration of primary crystals was continued even after the saturation of medium with the bridging liquid. The growth rates of primary crystals and agglomerates increased with an increase in the temperature and/or a reduction in the agitation speed of the system. The agglomerates were easily disintegrated into the primary crystals depositing ideally on carrier lactose particles for DPI by mixing. The in vitro efficiency of the mixed system of lactose and disintegrated primary crystals of drug was 2 to 3 times higher than that of crystals prepared conventionally. Furthermore, the soft agglomerates disintegrated easily into respirable particles in air stream when emitted from the inhalation device were prepared by reducing the agitation speed after the dispersing medium was saturated with the bridging liquid.