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Adv Drug Deliv Rev. 2008 Mar 17;60(6):673-91. Epub 2007 Nov 7.

Enhancing intestinal drug solubilisation using lipid-based delivery systems.

Author information

1
Department of Pharmaceutics, Victorian College of Pharmacy, Monash University (Parkville campus), Parkville, Victoria 3052, Australia. Chris.Porter@vcp.monash.edu.au

Abstract

Lipid-based delivery systems are finding increasing application in the oral delivery of poorly water-soluble, lipophilic drugs. Whilst lipidic dose forms may improve oral bioavailability via several mechanisms, enhancement of gastrointestinal solubilisation remains argueably the most important method of absorption enhancement. This review firstly describes the mechanistic rationale which underpins the use of lipid-based delivery systems to enhance drug solubilisation and briefly reviews the available literature describing increases in oral bioavailability after the administration of lipid solution, suspension and self-emulsifying formulations. The use of in vitro methods including dispersion tests and more complex models of in vitro lipolysis as indicators of potential in vivo performance are subsequently described, with particular focus on recent data which suggests that the digestion of surfactants present in lipid-based formulations may impact on formulation performance. Finally, a series of seven guiding principles for formulation design of lipid-based delivery systems are suggested based on an analysis of recent data generated in our laboratories and elsewhere.

PMID:
18155801
DOI:
10.1016/j.addr.2007.10.014
[Indexed for MEDLINE]

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