Spernath A; Aserin A (December 2006). "Microemulsions as carriers for drugs and nutraceuticals". Adv Colloid Interface Sci. 128–130: 47–64. doi:10.1016/j.cis.2006.11.016. PMID17229398.
Jing Q; Shen Y; Ren F; Chen J; Jiang Z; Peng B; Leng Y; Dong J (November 2006). "HPLC determination of anethole trithione and its application to pharmacokinetics in rabbits". J Pharm Biomed Anal. 42 (5): 613–7. doi:10.1016/j.jpba.2006.05.013. PMID16824723.
Zhang P; Liu Y; Feng N; Xu J (May 2008). "Preparation and evaluation of self-microemulsifying drug delivery system of oridonin". Int J Pharm. 355 (1–2): 269–76. doi:10.1016/j.ijpharm.2007.12.026. PMID18242895.
Liu Y; Zhang P; Feng N; Zhang X; Wu S; Zhao J (January 2009). "Optimization and in situ intestinal absorption of self-microemulsifying drug delivery system of oridonin". Int J Pharm. 365 (1–2): 136–42. doi:10.1016/j.ijpharm.2008.08.009. PMID18782611.
Cui J; Yu B; Zhao Y; Zhu W; Li H; Lou H; Zhai G (December 2008). "Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems". Int J Pharm. 371 (1–2): 148–55. doi:10.1016/j.ijpharm.2008.12.009. PMID19124065.
Cui SX; Nie SF; Li L; Wang CG; Pan WS; Sun JP (November 2008). "Preparation and Evaluation of Self-Microemulsifying Drug Delivery System Containing Vinpocetine". Drug Dev Ind Pharm. 35 (5): 603–611. doi:10.1080/03639040802488089. PMID19040178.
Borhade VB; Nair HA; Hegde DD (October 2008). "Development and Characterization of Self-Microemulsifying Drug Delivery System of Tacrolimus for Intravenous Administration". Drug Dev Ind Pharm. 35 (5): 619–630. doi:10.1080/03639040802498856. PMID18979309. S2CID7127624.
Borhade VB; Nair HA; Hegde DD; Barhate CR (November 2008). "Development and Validation of HPTLC Method for Estimation of Tacrolimus in Formulations". Drug Dev Ind Pharm. 35 (4): 440–448. doi:10.1080/03639040802430594. PMID19040177. S2CID97608266.
Attama AA; Nkemnele MO (November 2005). "In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homolipid from Capra hircus". Int J Pharm. 304 (1–2): 4–10. doi:10.1016/j.ijpharm.2005.08.018. PMID16198521.
Mandawgade SD; Sharma S; Pathak S; Patravale VB (October 2008). "Development of SMEDDS using natural lipophile: application to beta-Artemether delivery". Int J Pharm. 362 (1–2): 179–83. doi:10.1016/j.ijpharm.2008.06.021. PMID18652886.
Holm R; Porter CJ; Edwards GA; Müllertz A; Kristensen HG; Charman WN (September 2003). "Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides". Eur J Pharm Sci. 20 (1): 91–7. doi:10.1016/S0928-0987(03)00174-X. PMID13678797.
Ljusberg-Wahren H; Seier Nielsen F; Brogård M; Troedsson E; Müllertz A (July 2005). "Enzymatic characterization of lipid-based drug delivery systems". Int J Pharm. 298 (2): 328–32. doi:10.1016/j.ijpharm.2005.02.038. PMID15979260.
Goddeeris C; Coacci J; Van den Mooter G (May 2007). "Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds". Eur J Pharm Biopharm. 66 (2): 173–81. doi:10.1016/j.ejpb.2006.10.005. PMID17158039.
Goddeeris C; Van den Mooter G (September 2008). "Free flowing solid dispersions of the anti-HIV drug UC 781 with Poloxamer 407 and a maximum amount of TPGS 1000: investigating the relationship between physicochemical characteristics and dissolution behaviour". Eur J Pharm Sci. 35 (1–2): 104–13. doi:10.1016/j.ejps.2008.06.010. PMID18644442.
Yi T; Wan J; Xu H; Yang X (October 2008). "A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs". Eur J Pharm Biopharm. 70 (2): 439–44. doi:10.1016/j.ejpb.2008.05.001. PMID18603415.
Lu JL; Wang JC; Zhao SX; Liu XY; Zhao H; Zhang X; Zhou SF; Zhang Q (August 2008). "Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice". Eur J Pharm Biopharm. 69 (3): 899–907. doi:10.1016/j.ejpb.2008.02.023. PMID18434109.
Kang BK; Chon SK; Kim SH; Jeong SY; Kim MS; Cho SH; Lee HB; Khang G (November 2004). "Controlled release of paclitaxel from microemulsion containing PLGA and evaluation of anti-tumor activity in vitro and in vivo". Int J Pharm. 286 (1–2): 147–56. doi:10.1016/j.ijpharm.2004.08.008. PMID15501011.
Grove M; Müllertz A; Nielsen JL; Pedersen GP (June 2006). "Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides". Eur J Pharm Sci. 28 (3): 233–42. doi:10.1016/j.ejps.2006.02.005. PMID16650738.
Grove M; Müllertz A; Pedersen GP; Nielsen JL (May 2007). "Bioavailability of seocalcitol III. Administration of lipid-based formulations to minipigs in the fasted and fed state". Eur J Pharm Sci. 31 (1): 8–15. doi:10.1016/j.ejps.2007.01.007. PMID17383165.
Woo JS; Song YK; Hong JY; Lim SJ; Kim CK (February 2008). "Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers". Eur J Pharm Sci. 33 (2): 159–65. doi:10.1016/j.ejps.2007.11.001. PMID18178070.
Patel D; Sawant KK (December 2007). "Oral bioavailability enhancement of acyclovir by self-microemulsifying drug delivery systems (SMEDDS)". Drug Dev Ind Pharm. 33 (12): 1318–26. doi:10.1080/03639040701385527. PMID18097805. S2CID3119405.
Kang BK; Lee JS; Chon SK; Jeong SY; Yuk SH; Khang G; Lee HB; Cho SH (April 2004). "Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs". Int J Pharm. 274 (1–2): 65–73. doi:10.1016/j.ijpharm.2003.12.028. PMID15072783.
Meng J; Zheng L (September 2007). "Application of mixture experimental design to simvastatin apparent solubility predictions in the microemulsifion formed by self-microemulsifying". Drug Dev Ind Pharm. 33 (9): 927–31. doi:10.1080/03639040601003733. PMID17891578. S2CID37334831.
Cirri M; Mura P; Mora PC (August 2007). "Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems". Int J Pharm. 340 (1–2): 84–91. doi:10.1016/j.ijpharm.2007.03.021. PMID17531411.
Wu W; Wang Y; Que L (July 2006). "Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system". Eur J Pharm Biopharm. 63 (3): 288–94. doi:10.1016/j.ejpb.2005.12.005. PMID16527467.
Woo JS; Kim TS; Park JH; Chi SC (January 2007). "Formulation and biopharmaceutical evaluation of silymarin using SMEDDS". Arch. Pharm. Res. 30 (1): 82–9. doi:10.1007/BF02977782. PMID17328246. S2CID22169992.
Cui S; Zhao C; Chen D; He Z (May 2005). "Self-microemulsifying drug delivery systems (SMEDDS) for improving in vitro dissolution and oral absorption of Pueraria lobata isoflavone". Drug Dev Ind Pharm. 31 (4–5): 349–56. doi:10.1081/DDC-54309. PMID16093200. S2CID9408964.
Cui S; Zhao C; Tang X; Chen D; He Z (June 2005). "Study on the bioavailability of puerarin from Pueraria lobata isoflavone self-microemulsifying drug-delivery systems and tablets in rabbits by liquid chromatography-mass spectrometry". Biomed. Chromatogr. 19 (5): 375–8. doi:10.1002/bmc.460. PMID15627278.
Shen H; Zhong M (September 2006). "Preparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatin". J. Pharm. Pharmacol. 58 (9): 1183–91. doi:10.1211/jpp.58.9.0004. PMID16945176. S2CID22542504.
Ito Y; Kusawake T; Prasad YV; Sugioka N; Shibata N; Takada K (July 2006). "Preparation and evaluation of oral solid heparin using emulsifier and adsorbent for in vitro and in vivo studies". Int J Pharm. 317 (2): 114–9. doi:10.1016/j.ijpharm.2006.02.056. PMID16631328.
Wei L; Sun P; Nie S; Pan W (September 2005). "Preparation and evaluation of SEDDS and SMEDDS containing carvedilol". Drug Dev Ind Pharm. 31 (8): 785–94. doi:10.1080/03639040500216428. PMID16221613. S2CID12794172.
Heo MY; Piao ZZ; Kim TW; Cao QR; Kim A; Lee BJ (May 2005). "Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole". Arch. Pharm. Res. 28 (5): 604–11. doi:10.1007/BF02977766. PMID15974450. S2CID11978203.
Ito Y; Kusawake T; Ishida M; Tawa R; Shibata N; Takada K (June 2005). "Oral solid gentamicin preparation using emulsifier and adsorbent". J Control Release. 105 (1–2): 23–31. doi:10.1016/j.jconrel.2005.03.017. PMID15908031.
Sha X; Yan G; Wu Y; Li J; Fang X (April 2005). "Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells". Eur J Pharm Sci. 24 (5): 477–86. doi:10.1016/j.ejps.2005.01.001. PMID15784337.
Li P; Ghosh A; Wagner RF; Krill S; Joshi YM; Serajuddin AT (January 2005). "Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions". Int J Pharm. 288 (1): 27–34. doi:10.1016/j.ijpharm.2004.08.024. PMID15607255.
Kim HJ; Yoon KA; Hahn M; Park ES; Chi SC (May 2000). "Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone". Drug Dev Ind Pharm. 26 (5): 523–9. doi:10.1081/DDC-100101263. PMID10789064. S2CID32771754.
Zupančič, O; Partenhauser, A; Lam, H Th; Rohrer, J; Bernkop-Schnürch, A (2016). "Development and in vitro characterisation of an oral self-emulsifying delivery system for daptomycin". European Journal of Pharmaceutical Sciences. 81: 129–136. doi:10.1016/j.ejps.2015.10.005. PMID26485536.
Leonaviciute, G; Bernkop-Schnürch, A (2015). "Self-emulsifying drug delivery systems in oral (poly)peptide drug delivery". Expert Opin Drug Deliv. 12 (11): 1703–1716. doi:10.1517/17425247.2015.1068287. PMID26477549. S2CID21890042.
Friedl, H; Dünnhaupt, S; Hintzen, F; Waldner, C; Parikh, S; Pearson, JP; Wilcox, MD; Bernkop-Schnürch, A (2013). "Development and evaluation of a novel mucus diffusion test system approved by self-nanoemulsifying drug delivery systems". J Pharm Sci. 102 (12): 4406–4413. doi:10.1002/jps.23757. PMID24258284.
Sha, X; Yan, G; Wu, Y; Li, J; Fang, X (2005). "Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells". Eur J Pharm Sci. 24 (5): 477–486. doi:10.1016/j.ejps.2005.01.001. PMID15784337.
Hintzen, F; Perera, G; Hauptstein, S; Müller, C; Laffleur, F; Bernkop-Schnürch, A (2014). "In vivo evaluation of an oral self-microemulsifying drug delivery system (SMEDDS) for leuprorelin". Int J Pharm. 472 (1–2): 20–26. doi:10.1016/j.ijpharm.2014.05.047. PMID24879935.
Spernath A; Aserin A (December 2006). "Microemulsions as carriers for drugs and nutraceuticals". Adv Colloid Interface Sci. 128–130: 47–64. doi:10.1016/j.cis.2006.11.016. PMID17229398.
Jing Q; Shen Y; Ren F; Chen J; Jiang Z; Peng B; Leng Y; Dong J (November 2006). "HPLC determination of anethole trithione and its application to pharmacokinetics in rabbits". J Pharm Biomed Anal. 42 (5): 613–7. doi:10.1016/j.jpba.2006.05.013. PMID16824723.
Zhang P; Liu Y; Feng N; Xu J (May 2008). "Preparation and evaluation of self-microemulsifying drug delivery system of oridonin". Int J Pharm. 355 (1–2): 269–76. doi:10.1016/j.ijpharm.2007.12.026. PMID18242895.
Liu Y; Zhang P; Feng NP; Zhang X; Xu J (September 2008). "[Release kinetics of oridonin self-microemulsifying drug delivery system in vitro]". Zhongguo Zhong Yao Za Zhi (in Chinese). 33 (18): 2049–52. PMID19160780.
Liu Y; Zhang P; Feng N; Zhang X; Wu S; Zhao J (January 2009). "Optimization and in situ intestinal absorption of self-microemulsifying drug delivery system of oridonin". Int J Pharm. 365 (1–2): 136–42. doi:10.1016/j.ijpharm.2008.08.009. PMID18782611.
Cui J; Yu B; Zhao Y; Zhu W; Li H; Lou H; Zhai G (December 2008). "Enhancement of oral absorption of curcumin by self-microemulsifying drug delivery systems". Int J Pharm. 371 (1–2): 148–55. doi:10.1016/j.ijpharm.2008.12.009. PMID19124065.
Cui SX; Nie SF; Li L; Wang CG; Pan WS; Sun JP (November 2008). "Preparation and Evaluation of Self-Microemulsifying Drug Delivery System Containing Vinpocetine". Drug Dev Ind Pharm. 35 (5): 603–611. doi:10.1080/03639040802488089. PMID19040178.
Borhade VB; Nair HA; Hegde DD (October 2008). "Development and Characterization of Self-Microemulsifying Drug Delivery System of Tacrolimus for Intravenous Administration". Drug Dev Ind Pharm. 35 (5): 619–630. doi:10.1080/03639040802498856. PMID18979309. S2CID7127624.
Borhade VB; Nair HA; Hegde DD; Barhate CR (November 2008). "Development and Validation of HPTLC Method for Estimation of Tacrolimus in Formulations". Drug Dev Ind Pharm. 35 (4): 440–448. doi:10.1080/03639040802430594. PMID19040177. S2CID97608266.
Zhang BE; Lu WB; Chen WW (July 2008). "[Study on self-microemulsifying drug delivery system of Jiaotai Pill active components]". Zhong Yao Cai (in Chinese). 31 (7): 1068–71. PMID18973026.
Attama AA; Nkemnele MO (November 2005). "In vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homolipid from Capra hircus". Int J Pharm. 304 (1–2): 4–10. doi:10.1016/j.ijpharm.2005.08.018. PMID16198521.
Zhou XT; Wang J; Wang Y; Sun JY; Nie SF; Pan WS (April 2008). "[Design and in vitro evaluation of self-microemulsifying drug delivery systems for piroxicam]". Yao Xue Xue Bao (in Chinese). 43 (4): 415–20. PMID18664206.
Mandawgade SD; Sharma S; Pathak S; Patravale VB (October 2008). "Development of SMEDDS using natural lipophile: application to beta-Artemether delivery". Int J Pharm. 362 (1–2): 179–83. doi:10.1016/j.ijpharm.2008.06.021. PMID18652886.
Holm R; Porter CJ; Edwards GA; Müllertz A; Kristensen HG; Charman WN (September 2003). "Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides". Eur J Pharm Sci. 20 (1): 91–7. doi:10.1016/S0928-0987(03)00174-X. PMID13678797.
Ljusberg-Wahren H; Seier Nielsen F; Brogård M; Troedsson E; Müllertz A (July 2005). "Enzymatic characterization of lipid-based drug delivery systems". Int J Pharm. 298 (2): 328–32. doi:10.1016/j.ijpharm.2005.02.038. PMID15979260.
Goddeeris C; Coacci J; Van den Mooter G (May 2007). "Correlation between digestion of the lipid phase of smedds and release of the anti-HIV drug UC 781 and the anti-mycotic drug enilconazole from smedds". Eur J Pharm Biopharm. 66 (2): 173–81. doi:10.1016/j.ejpb.2006.10.005. PMID17158039.
Goddeeris C; Van den Mooter G (September 2008). "Free flowing solid dispersions of the anti-HIV drug UC 781 with Poloxamer 407 and a maximum amount of TPGS 1000: investigating the relationship between physicochemical characteristics and dissolution behaviour". Eur J Pharm Sci. 35 (1–2): 104–13. doi:10.1016/j.ejps.2008.06.010. PMID18644442.
Yi T; Wan J; Xu H; Yang X (October 2008). "A new solid self-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugs". Eur J Pharm Biopharm. 70 (2): 439–44. doi:10.1016/j.ejpb.2008.05.001. PMID18603415.
Lu JL; Wang JC; Zhao SX; Liu XY; Zhao H; Zhang X; Zhou SF; Zhang Q (August 2008). "Self-microemulsifying drug delivery system (SMEDDS) improves anticancer effect of oral 9-nitrocamptothecin on human cancer xenografts in nude mice". Eur J Pharm Biopharm. 69 (3): 899–907. doi:10.1016/j.ejpb.2008.02.023. PMID18434109.
Kang BK; Chon SK; Kim SH; Jeong SY; Kim MS; Cho SH; Lee HB; Khang G (November 2004). "Controlled release of paclitaxel from microemulsion containing PLGA and evaluation of anti-tumor activity in vitro and in vivo". Int J Pharm. 286 (1–2): 147–56. doi:10.1016/j.ijpharm.2004.08.008. PMID15501011.
Grove M; Müllertz A; Nielsen JL; Pedersen GP (June 2006). "Bioavailability of seocalcitol II: development and characterisation of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglycerides". Eur J Pharm Sci. 28 (3): 233–42. doi:10.1016/j.ejps.2006.02.005. PMID16650738.
Grove M; Müllertz A; Pedersen GP; Nielsen JL (May 2007). "Bioavailability of seocalcitol III. Administration of lipid-based formulations to minipigs in the fasted and fed state". Eur J Pharm Sci. 31 (1): 8–15. doi:10.1016/j.ejps.2007.01.007. PMID17383165.
Woo JS; Song YK; Hong JY; Lim SJ; Kim CK (February 2008). "Reduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteers". Eur J Pharm Sci. 33 (2): 159–65. doi:10.1016/j.ejps.2007.11.001. PMID18178070.
Patel D; Sawant KK (December 2007). "Oral bioavailability enhancement of acyclovir by self-microemulsifying drug delivery systems (SMEDDS)". Drug Dev Ind Pharm. 33 (12): 1318–26. doi:10.1080/03639040701385527. PMID18097805. S2CID3119405.
Kang BK; Lee JS; Chon SK; Jeong SY; Yuk SH; Khang G; Lee HB; Cho SH (April 2004). "Development of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogs". Int J Pharm. 274 (1–2): 65–73. doi:10.1016/j.ijpharm.2003.12.028. PMID15072783.
Meng J; Zheng L (September 2007). "Application of mixture experimental design to simvastatin apparent solubility predictions in the microemulsifion formed by self-microemulsifying". Drug Dev Ind Pharm. 33 (9): 927–31. doi:10.1080/03639040601003733. PMID17891578. S2CID37334831.
Cirri M; Mura P; Mora PC (August 2007). "Liquid spray formulations of xibornol by using self-microemulsifying drug delivery systems". Int J Pharm. 340 (1–2): 84–91. doi:10.1016/j.ijpharm.2007.03.021. PMID17531411.
Wu W; Wang Y; Que L (July 2006). "Enhanced bioavailability of silymarin by self-microemulsifying drug delivery system". Eur J Pharm Biopharm. 63 (3): 288–94. doi:10.1016/j.ejpb.2005.12.005. PMID16527467.
Woo JS; Kim TS; Park JH; Chi SC (January 2007). "Formulation and biopharmaceutical evaluation of silymarin using SMEDDS". Arch. Pharm. Res. 30 (1): 82–9. doi:10.1007/BF02977782. PMID17328246. S2CID22169992.
Wang DK; Shi ZH; Liu L; Wang XY; Zhang CX; Zhao P (2006). "Development of self-microemulsifying drug delivery systems for oral bioavailability enhancement of alpha-Asarone in beagle dogs". PDA J Pharm Sci Technol. 60 (6): 343–9. PMID17260899.
Cui S; Zhao C; Chen D; He Z (May 2005). "Self-microemulsifying drug delivery systems (SMEDDS) for improving in vitro dissolution and oral absorption of Pueraria lobata isoflavone". Drug Dev Ind Pharm. 31 (4–5): 349–56. doi:10.1081/DDC-54309. PMID16093200. S2CID9408964.
Cui S; Zhao C; Tang X; Chen D; He Z (June 2005). "Study on the bioavailability of puerarin from Pueraria lobata isoflavone self-microemulsifying drug-delivery systems and tablets in rabbits by liquid chromatography-mass spectrometry". Biomed. Chromatogr. 19 (5): 375–8. doi:10.1002/bmc.460. PMID15627278.
Yu AH; Zhai GX; Cui J; Liu H (August 2006). "[Preparation of puerarin solid self-microemulsion]". Zhong Yao Cai (in Chinese). 29 (8): 834–8. PMID17076244.
Cui SM; Zhao CS; He ZG (June 2007). "[Assessment of Pueraria lobata isoflavone with self-microemulsifying drug delivery systems in vitro and in vivo]". Zhong Yao Cai (in Chinese). 30 (6): 684–7. PMID17918441.
Shen HR; Li ZD; Zhong MK (November 2005). "[Preparation and evaluation of self-microemulsifying drug delivery systems containing atorvastatin]". Yao Xue Xue Bao (in Chinese). 40 (11): 982–7. PMID16499080.
Shen HR; Li ZD; Zhong MK (January 2006). "HPLC assay and pharmacokinetic study of atorvastatin in beagle dogs after oral administration of atorvastatin self-microemulsifying drug delivery system". Pharmazie. 61 (1): 18–20. PMID16454200.
Shen H; Zhong M (September 2006). "Preparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatin". J. Pharm. Pharmacol. 58 (9): 1183–91. doi:10.1211/jpp.58.9.0004. PMID16945176. S2CID22542504.
Ito Y; Kusawake T; Prasad YV; Sugioka N; Shibata N; Takada K (July 2006). "Preparation and evaluation of oral solid heparin using emulsifier and adsorbent for in vitro and in vivo studies". Int J Pharm. 317 (2): 114–9. doi:10.1016/j.ijpharm.2006.02.056. PMID16631328.
Wei L; Sun P; Nie S; Pan W (September 2005). "Preparation and evaluation of SEDDS and SMEDDS containing carvedilol". Drug Dev Ind Pharm. 31 (8): 785–94. doi:10.1080/03639040500216428. PMID16221613. S2CID12794172.
Heo MY; Piao ZZ; Kim TW; Cao QR; Kim A; Lee BJ (May 2005). "Effect of solubilizing and microemulsifying excipients in polyethylene glycol 6000 solid dispersion on enhanced dissolution and bioavailability of ketoconazole". Arch. Pharm. Res. 28 (5): 604–11. doi:10.1007/BF02977766. PMID15974450. S2CID11978203.
Ito Y; Kusawake T; Ishida M; Tawa R; Shibata N; Takada K (June 2005). "Oral solid gentamicin preparation using emulsifier and adsorbent". J Control Release. 105 (1–2): 23–31. doi:10.1016/j.jconrel.2005.03.017. PMID15908031.
Sha X; Yan G; Wu Y; Li J; Fang X (April 2005). "Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells". Eur J Pharm Sci. 24 (5): 477–86. doi:10.1016/j.ejps.2005.01.001. PMID15784337.
Li P; Ghosh A; Wagner RF; Krill S; Joshi YM; Serajuddin AT (January 2005). "Effect of combined use of nonionic surfactant on formation of oil-in-water microemulsions". Int J Pharm. 288 (1): 27–34. doi:10.1016/j.ijpharm.2004.08.024. PMID15607255.
Postolache P; Petrescu O; Dorneanu V; Zanini AC (2002). "Cyclosporine bioavailability of two physically different oral formulations". Eur Rev Med Pharmacol Sci. 6 (6): 127–31. PMID12776806.
Kim HJ; Yoon KA; Hahn M; Park ES; Chi SC (May 2000). "Preparation and in vitro evaluation of self-microemulsifying drug delivery systems containing idebenone". Drug Dev Ind Pharm. 26 (5): 523–9. doi:10.1081/DDC-100101263. PMID10789064. S2CID32771754.
Zupančič, O; Partenhauser, A; Lam, H Th; Rohrer, J; Bernkop-Schnürch, A (2016). "Development and in vitro characterisation of an oral self-emulsifying delivery system for daptomycin". European Journal of Pharmaceutical Sciences. 81: 129–136. doi:10.1016/j.ejps.2015.10.005. PMID26485536.
Leonaviciute, G; Bernkop-Schnürch, A (2015). "Self-emulsifying drug delivery systems in oral (poly)peptide drug delivery". Expert Opin Drug Deliv. 12 (11): 1703–1716. doi:10.1517/17425247.2015.1068287. PMID26477549. S2CID21890042.
Friedl, H; Dünnhaupt, S; Hintzen, F; Waldner, C; Parikh, S; Pearson, JP; Wilcox, MD; Bernkop-Schnürch, A (2013). "Development and evaluation of a novel mucus diffusion test system approved by self-nanoemulsifying drug delivery systems". J Pharm Sci. 102 (12): 4406–4413. doi:10.1002/jps.23757. PMID24258284.
Sha, X; Yan, G; Wu, Y; Li, J; Fang, X (2005). "Effect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cells". Eur J Pharm Sci. 24 (5): 477–486. doi:10.1016/j.ejps.2005.01.001. PMID15784337.
Hintzen, F; Perera, G; Hauptstein, S; Müller, C; Laffleur, F; Bernkop-Schnürch, A (2014). "In vivo evaluation of an oral self-microemulsifying drug delivery system (SMEDDS) for leuprorelin". Int J Pharm. 472 (1–2): 20–26. doi:10.1016/j.ijpharm.2014.05.047. PMID24879935.
Borhade VB; Nair HA; Hegde DD (October 2008). "Development and Characterization of Self-Microemulsifying Drug Delivery System of Tacrolimus for Intravenous Administration". Drug Dev Ind Pharm. 35 (5): 619–630. doi:10.1080/03639040802498856. PMID18979309. S2CID7127624.
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