Spray-dried dispersions (SDDs) of low-solubility drugs have been prepared using the polymer hydroxypropyl methylcellulose acetate succinate (HPMCAS). For a variety of drug structures, these SDDs provide supersaturation in in vitro dissolution determinations and large bioavailability increases in vivo. In bile-salt/lecithin in vitro solutions, these SDDs provide amorphous drug/polymer colloids and an increased concentration of free drug and drug in micelles relative to crystalline or amorphous drug. As dry powders, the SDDs are a single amorphous phase in which the drug remains amorphous and dispersed and does not crystallize over storage times relevant for practical drug products. A melting temperature (T m )/glass-transition temperature (T g ) (K/K) versus log P map for 139 compounds formulated as SDDs provides a perspective on an appropriate formulation strategy for low-solubility drugs with various physical properties.
The D85N genetic variant of bacteriorhodopsin (BR) displays a nearly permanent lifetime of the photochromic P(490) state. We present pump-probe measurements that demonstrate this behavior. However, diffraction efficiency measurements made from holograms recorded in a hydrated D85N film show markedly different decay behavior, suggesting that a molecular diffusion process is occurring in the film. Holograms recorded with different grating frequencies display correspondingly different decay times, thus supporting this hypothesis. A thin D85N film was fabricated that was chemically cross linked, resulting in the elimination of diffusion of BR molecules within the polymer matrix. This film exhibits a grating lifetime of the order of weeks or more, thus permitting the long-term holographic storage of information.
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