Improvement of Dissolution Rates of Poorly Water Soluble APIs Using Novel Spray Freezing into Liquid Technology
Spray freezing into liquid technology produced amorphous, porous particles of danazol and carbamazepine with significantly enhanced wetting and dissolution rates.
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This paper studied a novel particle-engineering approach, spray freezing into liquid (SFL), to enhance dissolution of poorly water-soluble APIs using model compounds danazol or carbamazepine, with or without excipients. Solutions were atomized beneath liquid nitrogen into frozen droplets, then lyophilized, and the resulting powders were characterized by X-ray diffraction, SEM, particle sizing, surface area, contact angle, and in vitro dissolution. SFL powders were amorphous and highly porous, with markedly improved wetting and dissolution (e.g., danazol/poloxamer 407 reaching ~99% dissolution at 10 minutes), and they showed good physical/chemical stability after 2 months at 25°C/60%RH. The main limitation is that the work demonstrates the technology using a small set of specific drug models and reports primarily physicochemical and dissolution outcomes without in vivo verification. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
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Cited by (5)
- Facile Preparation of Danazol Nanoparticles by High-Gravity Anti-solvent Precipitation (HGAP) Method 2009
- Supersaturation Produces High Bioavailability of Amorphous Danazol Particles Formed by Evaporative Precipitation into Aqueous Solution and Spray Freezing into Liquid Technologies 2006
- Rapid release tablet formulation of micronized danazol powder produced by spray-freezing into liquid (SFL) 2004
- Stable Amorphous Danazol Nanostructured Powders with Rapid Dissolution Rates Produced by Spray Freezing into Liquid 2004
- Rapid dissolving high potency danazol powders produced by spray freezing into liquid process 2003
Source provenance
- openalex
- last seen: 2026-05-14T06:06:51.801183+00:00