References
- Fasinu P, Pillay V, Ndesendo VM, et al. Diverse approaches for the enhancement of oral drug bioavailability. Biopharm Drug Dispos 2011;32:185–209
- Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 2001;46:3–26
- Hauss DJ. Oral lipid-based formulations. Adv Drug Deliv Rev 2007;59:667–76
- Singh SK, Verma PRP, Razdan B. Development and characterization of a lovastatin-loaded self-microemulsifying drug delivery system. Pharm Dev Technol 2010;15:469–83
- Chan VS. Nanomedicine: an unresolved regulatory issue. Regul Toxicol Pharmacol 2006;46:218–24
- Wei Y, Ye X, Shang X, et al. Enhanced oral bioavailability of silybin by a supersaturable self-emulsifiyng drug delivery system (S-SEDDS). Colloids Surf A Physiochem Eng Aspects 2012;396:22–8
- Gursoy RN, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacotherapy 2004;58:173–82
- Gershanik T, Benita S. Self-dispersing lipid formulations for lipophilic drugs. Eur J Pharm Biopharm 2000;50:179–88
- Constantinides P. Lipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspects. Pharm Res 1995;12:1561–72
- Porter CJH, Pouton CW, Cuine JF, Charman WN. Enhancing intestinal drug solubilisation using lipid-based delivery systems. Adv Drug Deliv Rev 2008;60:673–91
- Chen XQ, Gudmundsson OS, Hageman MJ. Application of lipid-based formulations in drug discovery. J Med Chem 2012;55:7945–56
- Nazzal S, Khan MA. Controlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parameters. Int J Pharm 2006;315:110–21
- Dixit RP, Nagarsenker MS. Self-nanoemulsifying granules of ezetimibe: design, optimization and evaluation. Eur J Pharm Sci 2008;35:183–92
- Deshmukh A, Kulkarni S. Solid self-microemulsifying drug delivery system of ritonavir. Drug Dev Ind Pharm 2013. [Epub ahead of print]. DOI:10.3109/03639045.2013.768632
- Singh SK, Verma PRP, Razdan B. Glibenclamide-loaded self-nanoemulsifying drug delivery system: development and characterization. Drug Dev Ind Pharm 2010;36:933–45
- Bajaj A, Rao MRP, Khole I, Munjapara G. Self-nanoemulsifying drug delivery system of cefpodoxime proxetil containing tocopherol polyethylene glycol succinate. Drug Dev Ind Pharm 2013;39:635–45
- Gupta S, Chavhan S, Sawant KK. Self-nanoemulsifying drug delivery system for adefovir dipivoxil: design, characterization, in vitro and ex vivo evaluation. Coll Surf A: Physiochem Eng Aspects 2011;392:145–55
- Bourkaib N, Zhou J, Yao J, et al. Combination of β-cyclodextrin inclusion complex and self-microemulsifying drug delivery system for photostability and enhanced oral bioavailbility of methotrexate: novel technique. Drug Dev Ind Pharm 2013;39:918–27
- Balakrishnan P, Lee BJ, Oh DJ, et al. Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS). Eur J Pharm Biopharm 2009;72:539–45
- Beg S, Jena SS, Patra CN, et al. Development of solid self-nanoemulsifying granules (SSNEGs) of ondansetron hydrochloride with enhanced bioavailability potential. Coll Surf B: Biointerfaces 2013;101:414–13
- Dejaegher B, Heyden YV. Experimental designs and their recent advances in set-up, data interpretation, and analytical applications. J Pharm Biomed Anal 2011;56:141–58
- Ren S, Mu H, Alchau F, et al. Optimization of self-nanoemulsifying drug delivery system for poorly water soluble drugs using response surface methodology. Drug Dev Ind Pharm 2013;39:799–806
- Martindale. The extra pharmacopoeia. 33rd ed. London: The Pharmaceutical Press; 1989
- Zhang J, Bunker M, Parker A, et al. The stability of solid dispersions of felodipine in polyvinylpyrrolidone characterized by nanothermal analysis. Int J Pharm 2011;414:210–17
- Karavas E, Georgarakis E, Bikiaris D. Felodipine nanodispersions as active core for predictable pulsatile chronotherapeutics using PVP/HPMC blends as coating layer. Int J Pharm 2006;313:189–97
- Patil PR, Biradar SV, Paradkar AR. Extended release felodipine self-nanoemulsifying system. AAPS Pharm Sci Tech 2009;10:515–23
- Bhagat C, Singh SK, Verma PRP, et al. Crystalline and amorphous carvedilol-loaded nanoemulsions: formulation, optimization using response surface methodology. J Exp Nanosci; 2011. Available from: http://dx.doi.org/10.1080/17458080.2011.630037
- Zidan AS, Sammour OA, Hammad MA, et al. Quality by design: understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box–Behnken design and desirability function. Int J Pharm 2007;332:55–63
- Kommuru TR, Gurley B, Khan MA, Reddy IK. Self-emulsifying drug delivery systems (SEDDS) of Coenzyme Q10: formulation development and bioavailability assessment. Int J Pharm 2001;212:233–46
- Khoo SK, Humberstone AJ, Porter JH, et al. Formulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrine. Int J Pharm 1998;167:155–64
- Singh SK, Verma PRP, Razdan B. Atomic force microscopy, transmission electron microscopy, and photon correlation spectroscopy: three techniques for rapid characterization of optimized self-nanoemulsifying drug delivery system of glibenclamide, carvedilol, and lovastatin. J Disp Sci Tech 2011;32:538–45
- Sajjadi S. Nanoemulsion formation by phase inversion emulsification: on the nature of inversion. Langmuir 2006;22:5597–603
- Kallakunta VR, Bandari S, Jukanti R, Veerareddy PR. Oral self-emulsifying powder of lercanidipine hydrochloride: formulation and evaluation. Powder Technol 2012;221:375–82
- Aulton ME, Wells TI, eds. Pharmaceutics: the science of dosage form design. 2nd ed. London: Churchill Livingston; 2002, Chapter 8
- Shanmugam S, Baskaran R, Balakrishnan P, et al. Solid self-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein. Eur J Pharm Biopharm 2011;79:250–7
- Yi T, Wan J, Xu H, Yang X. Controlled poorly soluble drug release from solid self-microemulsifying formulations with high density hydroxypropylmethylcellulose. Eur J Pharm Sci 2008;34:274–80
- Pouton CW. Formulation of self-emulsifying drug delivery systems. Adv Drug Deliv Rev 1997;25:47–58
- Zhao Y, Wang C, Chow AHL, et al. Self-nanoemulsifying drug delivery system (SNEDDS) for oral delivery of Zeodary essential oil: formulation and bioavailability studies. Int J Pharm 2010;383:170–7
- Fatouros DG, Bergenstahl B, Mullertz A. Morphological observations on a lipid-based drug delivery system during in vitro digestion. Eur J Pharm Sci 2007;31:85–94
- Preetz C, Hauser A, Hause G, et al. Application of atomic force microscopy and ultrasonic resonator technology on nanoscale: distinction of nanoemulsions from nanocapsules. Eur J Pharm Sci 2010;39:141–51