2Shah NH, Carvajal MT, Patel CI, et al. Self-emulsifying drug delivery systems(SEDDS)with polyglycolyzed glycerides for improvingin vitro dissolution and oral absorption of lipophilic drugs[ J ]. Int J Pharm,1994,106( 1 ): 15.
3Yamada I, Goda T, Kawata M, et al.Application of gastric aciditycontrolled beagle dog to bioavailability study of cinnarizine [ J ].Yakugaku Zasshi , 1990,110(4): 280.
4Constantinides PP. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects [ J ].Pharm Res, 1995,12( 11 ): 1561.
8Tomi J,Kristiina J,Nancy S,et al.β-cyclodextrin derivatives,SBE4-β-CD and HP-β-CD,increase the oral bioavailability of cinnarizine in beagle dogs.. Journal of Pharmacological Sciences . 1995
9Gupta PK,Hung CT.Quantitative evaluation of targeted drug delivery systems. International Journal of Pharmaceutics . 1989
10GIPPS EM,Arshady RE,Kreuter J,et al.Distribution of polyhexyl cyanoacrylate nanoparticles in nude mice bearing human osteosarcoma. Journal of Pharmacological Sciences . 1986