Literature DB >> 28673096

Review and analysis of FDA approved drugs using lipid-based formulations.

Ronak Savla1, Jeff Browne2, Vincent Plassat3, Kishor M Wasan4, Ellen K Wasan4.   

Abstract

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.

Entities:  

Keywords:  Lipid-based drug delivery systems; biopharmaceutics; clinical translation; developability classification system; physicochemical properties

Mesh:

Substances:

Year:  2017        PMID: 28673096     DOI: 10.1080/03639045.2017.1342654

Source DB:  PubMed          Journal:  Drug Dev Ind Pharm        ISSN: 0363-9045            Impact factor:   3.225


  22 in total

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4.  Stereospecific synthesis of phosphatidylglycerol using a cyanoethyl phosphoramidite precursor.

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8.  Suitability of Artificial Membranes in Lipolysis-Permeation Assays of Oral Lipid-Based Formulations.

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