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- W51494704 endingPage "514" @default.
- W51494704 startingPage "487" @default.
- W51494704 abstract "Dissolution test is an extremely valuable and powerful tool in understanding the parameters that control dissolution of amorphous formulations as well as in revealing supersaturation effect and the solid-state transformations that might occur after oral administration. Supersaturated/non-sink and biorelevant dissolution conditions could guide in designing the solid dispersion in order to select optimal polymer(s), drug loading, and downstream processing for the desired in vivo performance as well as shelf life stability. The focus of this chapter is to review and describe the different models being used to characterize dissolution of solid oral dosage forms containing amorphous drugs in aqueous and biorelevant media. Dissolution case studies of weak base, weak acid, and neutral compounds are presented, illustrating a rational approach for the development and implementation of the desired dissolution characteristics for the amorphous drug product performance. Finally, case studies of successful in vitro–in vivo correlations of amorphous formulations are presented. This chapter can serve as guidance for the development and understanding of dissolution of amorphous solid dispersions." @default.
- W51494704 created "2016-06-24" @default.
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- W51494704 date "2014-01-01" @default.
- W51494704 modified "2023-10-05" @default.
- W51494704 title "Dissolution of Amorphous Solid Dispersions: Theory and Practice" @default.
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- W51494704 doi "https://doi.org/10.1007/978-1-4939-1598-9_15" @default.
- W51494704 hasPublicationYear "2014" @default.