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Drug development and industrial pharmacy, 2017-11, Vol.43 (11), p.1743-1758
2017
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Details

Autor(en) / Beteiligte
Titel
Review and analysis of FDA approved drugs using lipid-based formulations
Ist Teil von
  • Drug development and industrial pharmacy, 2017-11, Vol.43 (11), p.1743-1758
Ort / Verlag
England: Taylor & Francis
Erscheinungsjahr
2017
Quelle
EBSCOhost Business Source Ultimate
Beschreibungen/Notizen
  • Lipid-based drug delivery systems (LBDDS) are one of the most studied bioavailability enhancement technologies and are utilized in a number of U.S. Food and Drug Administration (FDA) approved drugs. While researchers have used several general rules of thumb to predict which compounds are likely to benefit from LBDDS, formulation of lipid systems is primarily an empiric endeavor. One of the challenges is that these rules of thumb focus in different areas and are used independently of each other. The Developability Classification System attempts to link physicochemical characteristics with possible formulation strategies. Although it provides a starting point, the formulator still has to empirically develop the formulation. This article provides a review and quantitative analysis of the molecular properties of these approved drugs formulated as lipid systems and starts to build an approach that provides more directed guidance on which type of lipid system is likely to be the best for a particular drug molecule.

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