1. Dressman JB, Reppas C. In vitro-in vivo correlations for lipophilic, poorly water-soluble drugs. Eur J Pharm Sci. 2000;11(Suppl):573–80.
2. Fujioka Y, Kadono K, Fujie Y, Metsugi Y, Ogawara K, Higaki K, et al. Prediction of oral absorption of griseofulvin, a BCS class II drug, based on GITA model: utilization of a more suitable medium for in-vitro dissolution study. J Control Rel. 2008;352:36–43.
3. Fujioka Y, Metsugi Y, Ogawara K, Higaki K, Kimura T. Evaluation of in-vivo dissolution behavior and GI transit of griseofulvin, a BCS class II drug. Int J Pharm. 2008;352:36–43.
4. Serajuddin ATM. Solid dispersion of poorly water-soluble drugs: early promises, subsequent problems, and recent breakthroughs. J Pharm Sci. 1999;88:1058–66.
5. Grove M, Müllertz A. Liquid self-microemulsifying drug delivery system. In: Hauss DJ, editor. Oral lipid-based formulations. New York: Informa; 2007. p. 107–27.