| Literature DB >> 28057543 |
Mette D Mosgaard1, Philip J Sassene1, Huiling Mu1, Thomas Rades1, Anette Müllertz2.
Abstract
The high-throughput in vitro intestinal lipolysis model (HTP) applicable for rapid and low-scale screening of lipid-based drug delivery systems (LbDDSs) was optimized and adjusted as to be conducted in 96-well plates (HTP-96). Three different LbDDSs (I-III) loaded with danazol or cinnarizine were used as model systems. The distributions of cinnarizine and danazol in the aqueous and precipitated digestion phases generated during lipolysis in HTP-96 were compared with previously published data obtained from HTP. The final HTP-96 setup resulted in the same rank order as the original HTP model with regard to solubilization in the aqueous phase during digestion: LbDDS III > LbDDS II > LbDDS I for danazol and LbDDS III ≈ LbDDS II ≈ LbDDS I for cinnarizine. HTP-96 is a useful model for fast performance assessment of LbDDS in a small scale.Entities:
Keywords: dissolution; emulsions; formulation; gastrointestinal; high throughput technologies; in vitro model; lipids; microemulsions; oral drug delivery; precipitation; solubility
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Year: 2017 PMID: 28057543 DOI: 10.1016/j.xphs.2016.12.026
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534