6Tatyana Gershanik,Sharon Benzeno,Simon Benita. Interaction of a Self-Emulsifying Lipid Drug Delivery System with the Everted Rat Intestinal Mucosa as a Function of Droplet Size and Surface Charge[J] 1998,Pharmaceutical Research(6):863～869 被引量：1
二级参考文献19
1[1]Pouton, C. W. Formulation of self-emulsifying drug delivery systems[J]. Adv Drug Deliv Rev. 1997,25:47-58. 被引量：1
2[2]Constantinides PP. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceuticai aspects[J]. Pharm Res. 1995,12: 1561-1572. 被引量：1
3[3]Holmberg I, Aksnes L, Berlin T, et al. Absorption of a pharmacological dose of vitamin D3 from two different lipid vehicles in man :comparison of peanut oil and a medium-chain Triglyceride[J]. Biopharm Drug Disposition, 1990, 11: 807-815. 被引量：1
4[4]Shah NH, Carvajal MT, Patal CI, et al. Self-emulsifying drug delivery systems (SEDDS)with polyglycolyzed glycerides for improving in vitro dissolution and oral absorption of lipophilic drugs[J]. Int J Pharm, 1994,106: 15-23. 被引量：1
5[5]Pouton CW. Self-emulsifying drug delivery systems :assessment of the efficiency of emulsification[J]. Int J Pharm,1985,27: 335-348. 被引量：1
6[6]Pouton CW. Effects of inclusion of a model drug on the performance of Self-emulsifying formulations[J]. J Pharm Pharmac, 1984,36 : 51P. 被引量：1
7[7]Charman SA, Charman WN, Rogge MC, et al. Self-emulsifying drug delivery systems: Formulation and biopharmaceutic evaluation of an investigational lipophilic compound[J].Pharm Res, 1992,9 (1):87-93. 被引量：1
8[8]Lievens L, Hildegard SR. Pharmaceutical formulations of benzodiazepines [ P]. European Patent Application EP , 0 517412 A1,1992. 被引量：1
9[9]Gershanik T, Benita S. Positively charged self-emulsifying oil formulation for improving oral bioavailability of progesterone[J]. Pharm Dev and Tech, 1996,1(2):147-157. 被引量：1
10[10]Gershanik T, Benzeno S,Benita S. Interaction of a selfemulsifying lipid drug delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge[J]. Pharm Res, 1998,15(6): 863-869. 被引量：1
4Kim M S, Kim J S, You Y H, et al. Development and optimization of a novel oral controlled delivery system for tamsulosin hydrochloride using response surface methodology [J]. Int J Pharm, 2007, 341(1/2): 97-104. 被引量：1
5Hong J Y, Kim J K, Song Y K, et al. A new self2emulsifying formulation of it raconazole with improved dissolution and oral absorption [J]. J Cont roll Rel, 2006, 110(2): 332-338. 被引量：1
6Hows M E P, Perrett D, Kay D J. Optimisation of a simultaneous separation of sulphonamides, dihydrofolate reductase inhibitors and β-lactam antibiotics by capillary electrophoresis [J]. J Chromatogr A, 1997, 768: 97-105. 被引量：1
7Gursoy R N, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs [J]. Biomed Pharmacother, 2004, 58(3): 173-182. 被引量：1
