In vitro and in vivo evaluation of a self-microemulsifying drug delivery system for the poorly soluble drug fenofibrate

Author:

Cho Young-Dae,Park Young-Joon

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Drug Discovery,Molecular Medicine

Reference32 articles.

1. Charman, S.A., W.N. Charman, M.C. Rogge, T.D. Wilson, F.J. Dutko, and C.W. Pouton. 1992. Self-emulsifying drug delivery systems: formulation and biopharmaceutic evaluation of an investigational lipophilic compound. Pharmaceutical Research 9: 87–93.

2. Chi, S.C. 1999. Enhanced dissolution rate of biphenyl dimethyl dicarboxylate using SMEDDS. Bulletin Technique Gattefossé 92: 75–80.

3. Constantinides, P.P. 1995. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharmaceutical Research 12: 1561–1572.

4. Craig, D.M.Q. 1993. The use of self-emulsifying systems as a means of improving drug delivery. Bulletin Technique Gattefossé 86: 21–31.

5. Curtet B, Teillaud E, Reginault P (1980) inventors. Fournier Innovation et Synergie, assignee. Novel dosage form of fenofibrate. US patent 4895726., January 23.

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