[1] Carrier RL,Miller LA,Ahmed I. The utility of cyclodextrins for enhancing oral bioavailability[J].J Contr Release,2007,123(2):78-99.
[2] Gursoy RN,Benita S. Self-emulsifying drug delivery systems(SEDDS) for improved oral delivery of lipophilic drugs[J].Biomed Pharmacother,2004,58(3):173-182.
[3] Tang B,Cheng G,Gu J,et al. Development of solid self-microemulsifying drug delivery systems:preparation techniques and dosage forms[J].Drug Discov Today,2008,13(14):606-612.
[4] Gershanik T,Benita S. Self-dispersing lipid formulations for improving oral absorption of lipophilic drugs[J].Eur J Pharm Biopharm,2000,50(1):179-188.
[5] 崔 晶.姜黄素固体自微乳化制剂的研究[D].山东:山东大学,2006.
[6] Yi T,Wan J,Xu H,et al. A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs[J].Eur J Pharm Biopharm,2008,70(2):439-444.
[7] Mladen M,Jelena D,Ljiljana D,et al. Characterization and evaluation of solid self-microemulsifying drug delivery systems with porous carriers as systems for improved carbamazepine release[J].Int J Pharm,2012,436(1-2):58-65.
[8] Nazzal S,Nutan M,Palamakula A,et al. Optimization of a self-nanoemulsified tablet dosage form of ubiquinone using response surface methodology:effect of formulation ingredients[J].Int J Pharm,2002,240(1-2):103-114.
[9] Kallakunta VR,Bandari S,Jukanti R,et al. Oral self emulsifying powder of lercanidipine hydrochloride:formulation and evaluation[J].Powder Technol,2012,221:375-382.
[10] Shah AV,Serajuddin ATM. Development of solid self-emulsifying drug delivery system (SEDDS)I:use of poloxamer 188 as both solidifying and emulsifying agent for lpids[J].Pharm Res,2012,29(10):2817-2832.
[11] Hitesh C.B,Rajendra. CD,Harinath NM,et al. Design and optimization of chlordiazepoxide solid self-microemulsifying drug delivery system[J].Pharm Res,2011,4(2):369-372.
[12] Balakrishnan P,Lee BJ,Oh DH,et al. Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS)[J].Eur J Pharm Biopharm,2009,72 (3):539-545.
[13] Abdalla A,Mader K. Preparation and characterization of a self-emulsifying pellet formulation[J].Eur J Pharm Biopharm,2007,66(2):220-226.
[14] Wang Z,Sun J,Wang Y,et al. Solid self-emulsifying nitrendipine pellets:Preparation and in vitro/in vivo evaluation[J].Int J Pharm,2010,383(1-2):1-6.
[15] Hu X,Lin C,Chen D,et al. Sirolimus solid self-microemulsifying pellets:formulation development,characterization and bioavailability evaluation[J].Int J Pharm,2012,438(1-2):123-133.
[16] 易 涛. 固体自微乳化给药系统的研究[D].湖北:华中科技大学,2008.
[17] 何吉奎. 黄连素自微乳化肠溶胶珠的研究[D].重庆:西南大学,2011.
[18] Zhang Y,Wang RR,Wu J,et al. Characterization and evaluation of self-microemulsifying sustained-release pellet formulation of puerarin for oral delivery[J].Int J Pharm,2012,427(2):337-344.
[19] Xie H,Zhou W. Preparation of bi-layered solid self-microemulsifying tablets of tetra-acetylated puerarin[J].Chin J New Drugs,2011,20(9):837-843.
[20] Patil P,Joshi P,Paradkar A. Effect of formulation variables on preparation and evaluation of gelled self-emulsifying drug delivery system (SEDDS) of ketoprofen[J]. AAPS Pharm Sci Techn,2004,5 (3):E42.
[21] Serratoni M,Newton M,Booth S,et al. Controlled drug release from pellets containing water insoluble drugs dissolved in a self-emulsifying system[J].Eur J Pharm Biopharm,2007,65 (1):94-98.