1. |
Di L, Fish PV, Mano T. Bridging solubility between drug discovery and development. Drug Discov Today 2012;17:486-95.
|
2. |
Bergström CA, Holm R, Jørgensen SA, Andersson SB, Artursson P, Beato S, et al. Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs. Eur J Pharm Sci 2014;57:173-99.
|
3. |
Custodio JM, Wu CY, Benet LZ. Predicting drug disposition, absorption/elimination/transporter interplay and the role of food on drug absorption. Adv Drug Deliv Rev 2008;60:717-33.
|
4. |
Sauron R, Wilkins M, Jessent V, Dubois A, Maillot C, Weil A, et al. Absence of a food effect with a 145 mg nanoparticle fenofibrate tablet formulation. Int J Clin Pharmacol Ther 2006;44:64-70.
|
5. |
Sanganwar GP, Gupta RB. Dissolution-rate enhancement of fenofibrate by adsorption onto silica using supercritical carbon dioxide. Int J Pharm 2008;360:213-8.
|
6. |
Wishart DS, Knox C, Guo AC, Shrivastava S, Hassanali M, Stothard P, et al. DrugBank: A comprehensive resource for in silico drug discovery and exploration. Nucleic Acids Res 2006;34:D668-72.
|
7. |
Ming-Thau S, Ching-Min Y, Sokoloski TD. Characterization and dissolution of fenofibrate solid dispersion systems. Int J Pharm 1994;103:137-46.
|
8. |
Löbenberg R, Amidon GL. Modern bioavailability, bioequivalence and biopharmaceutics classification system. New scientific approaches to international regulatory standards. Eur J Pharm Biopharm 2000;50:3-12.
|
9. |
Guay DR. Micronized fenofibrate: A new fibric acid hypolipidemic agent. Ann Pharmacother 1999;33:1083-103.
|
10. |
Granero GE, Ramachandran C, Amidon GL. Dissolution and solubility behavior of fenofibrate in sodium lauryl sulfate solutions. Drug Dev Ind Pharm 2005;31:917-22.
|
11. |
Badens E, Majerik V, Horváth G, Szokonya L, Bosc N, Teillaud E, et al. Comparison of solid dispersions produced by supercritical antisolvent and spray-freezing technologies. Int J Pharm 2009;377:25-34.
|
12. |
Leuner C, Dressman J. Improving drug solubility for oral delivery using solid dispersions. Eur J Pharm Biopharm 2000;50:47-60.
|
13. |
Perrut M, Jung J, Leboeuf F. Enhancement of dissolution rate of poorly-soluble active ingredients by supercritical fluid processes. Part I: Micronization of neat particles. Int J Pharm 2005;288:3-10.
|
14. |
Junghanns JU, Müller RH. Nanocrystal technology, drug delivery and clinical applications. Int J Nanomedicine 2008;3:295-309.
|
15. |
Williams HD, Trevaskis NL, Yeap YY, Anby MU, Pouton CW, Porter CJ, et al. Lipid-based formulations and drug supersaturation: Harnessing the unique benefits of the lipid digestion/absorption pathway. Pharm Res 2013;30:2976-92.
|
16. |
O'Reilly JR, Corrigan OI, O'Driscoll CM. The effect of mixed micellar systems, bile acid/fatty acids, on the solubility and intestinal absorption of clofazimine (B663) in the anaesthetized rat. Int J Pharm 1994;109:147-54.
|
17. |
Srinarong P, Faber JH, Visser MR, Hinrichs WL, Frijlink HW. Strongly enhanced dissolution rate of fenofibrate solid dispersion tablets by incorporation of superdisintegrants. Eur J Pharm Biopharm 2009;73:154-61.
|
18. |
Patel AR, Vavia PR. Effect of hydrophilic polymer on solubilization of fenofibrate by cyclodextrin complexation. J Incl Pheno Macrocycl Chem 2006;56:247-51.
|
19. |
Wei LL, Peixin, W Chandra N, Say Chye JL. Gastric-floating microcapsules provide controlled and sustained release of multiple cardiovascular drugs, J Mater Chem 2013;1:1090-5.
|
20. |
Bhargava P, Bhargava S, Daharwal SJ. Self emulsifying drug delivery system: An approach to improve the solubility of poorly water soluble drug. Adv Res Pharm Biol 2011;1:1-9.
|
21. |
Yamada K, Yamashita J, Todo H, Miyamoto K, Hashimoto S, Tokudome Y, et al. Preparation and evaluation of liquid-crystal formulations with skin-permeation-enhancing abilities for entrapped drugs. J Oleo Sci 2011;60:31-40.
|
22. |
Clogston J, Rathman J, Tomasko D, Walker H, Caffrey M. Phase behavior of a monoacylglycerol: (myverol 18-99K)/water system. Chem Phys Lipids 2000;107:191-220.
|
23. |
Lian R, Lu Y, Qi J, Tan Y, Niu M, Guan P, et al. Silymarin glyceryl monooleate/poloxamer 407 liquid crystalline matrices: Physical characterization and enhanced oral bioavailability. AAPS PharmSciTech 2011;12:1234-40.
|
24. |
Drummond CJ, Fong C. Surfactant self-assembly objects as novel drug delivery vehicles. Curr Opin Colloid Interf Sci 1999;4:449-56.
|
25. |
Chung H, Kim J, Um JY, Kwon IC, Jeong SY. Self-assembled “nanocubicle” as a carrier for peroral insulin delivery. Diabetologia 2002;45:448-51.
|
26. |
Lopes LB, Lopes JL, Oliveira DC, Thomazini JA, Garcia MT, Fantini MC, et al. Liquid crystalline phases of monoolein and water for topical delivery of cyclosporin A: Characterization and study of in vitro and in vivo delivery. Eur J Pharm Biopharm 2006;63:146-55.
|
27. |
Boyd BJ, Whittaker DV, Khoo SM, Davey G. Lyotropic liquid crystalline phases formed from glycerate surfactants as sustained release drug delivery systems. Int J Pharm 2006;309:218-26.
|
28. |
Norling T, Lading P, Engström S, Larsson K, Krog N, Nissen SS, et al. Formulation of a drug delivery system based on a mixture of monoglycerides and triglycerides for use in the treatment of periodontal disease. J Clin Periodontol 1992;19:687-92.
|
29. |
Gustafsson J, Ljusberg-Wahren H, Almgren M, Larsson K. Submicron particles of reversed lipid phases in water stabilized by a nonionic amphiphilic polymer. Langmuir 1997;13:6964-71.
|
30. |
Briggs J, Caffrey M. The temperature-composition phase diagram and mesophase structure characterization of monopentadecenoin in water. Biophys J 1994;67:1594-602.
|
31. |
Barauskas J, Landh T. Phase behaviour of the phytantriol/water system, Langmuir. 2003;19:9562-5.
|
32. |
Hato M, Minamikawa H. The effects of oligosaccharide stereochemistry on the physical properties of aqueous synthetic glycolipids. Langmuir 1996;12:1658-65.
|
33. |
Charman WN, Rogge MC, Boddy AW, Berger BM. Effect of food and a monoglyceride emulsion formulation on danazol bioavailability. J Clin Pharmacol 1993;33:381-6.
|
34. |
Ermer J. Performance parameters, calculation and tests. In: Ermer J, Miller J, editors. Method validation in Pharmaceutical Analysis. New York: Wiley-VCH, Verlag GMBH; 2005. p. 21-119.
|
35. |
Nesseem DI. Formulation and evaluation of itraconazole via liquid crystal for topical delivery system. J Pharm Biomed Anal 2001;26:387-99.
|
36. |
Ghosh PK, Majithiya RJ, Umrethia ML, Murthy RS. Design and development of microemulsion drug delivery system of acyclovir for improvement of oral bioavailability. AAPS PharmSciTech 2006;7:77.
|
37. |
Tilley AJ, Drummond CJ, Boyd BJ. Disposition and association of the steric stabilizer pluronic® F127 in lyotropic liquid crystalline nanostructured particle dispersions. J Colloid Interface Sci 2013;392:288-96.
|
38. |
Chong JY, Mulet X, Waddington LJ, Boyd BJ, Drummond CJ. Steric stabilisation of self-assembled cubic lyotropic liquid crystalline nanoparticles: High throughput evaluation of triblock polyethene oxide-polypropylene oxide-polyethene oxide copolymers, Soft Matter 2011;7:4768.
|
39. |
Dong YD, Larson I, Hanley T, Boyd BJ. Bulk and dispersed aqueous phase behavior of phytantriol: Effect of Vitamin E acetate and F127 polymer on liquid crystal nanostructure. Langmuir 2006;22:9512-8.
|
40. |
Alam MM, Sugiyama Y, Watanabe K, Aramaki K. Phase behavior and rheology of oil-swollen micellar cubic phase and gel emulsions in nonionic surfactant systems. J Colloid Interface Sci 2010;341:267-72.
|
41. |
Milak S, Zimmer A. Glycerol monooleate liquid crystalline phases used in drug delivery systems. Int J Pharm 2015;478:569-87.
|
42. |
Wei S, Ren J, Li N, Huo W, Gao C. Preparation and pharmacokinetic study of fenofibrate cubic liquid crystalline. Asian J Pharm Sci 2017;17:30193-9.
|