In situ formation of nanocrystals from a self-microemulsifying drug delivery system to enhance oral bioavailability of fenofibrate

References

• HoarTPSchulmanJHTransparent water in oil dispersions: oleopathic hydromicelleNature1943152102105
   Google Scholar
• SpernathAAserinAMicroemulsions as carriers for drugs and nutraceuticalsAdv Colloid Interface Sci2006128–1304764
   PubMed Web of Science ®Google Scholar
• LyonsKCCharmanWNMillerRPorterCJFactors limiting the oral bioavailability of N-acetylglucosaminyl-N-acetylmuramyl dipeptide (GMDP) and enhancement of absorption in rats by delivery in a water-in- oil microemulsionInt J Pharm2000199172810794923
   PubMed Web of Science ®Google Scholar
• HuZPTawaRKonishiTShibataNTakadaKA novel emulsifier, Labrasol, enhances gastrointestinal absorption of gentamicinLife Sci2001692899291011720093
   PubMed Web of Science ®Google Scholar
• KawakamiKYoshikawaTHayashiTNishiharaYMasudaKMicroemulsion formulation for enhanced absorption of poorly soluble drugs. II. In vivo studyJ Control Release200281758211992680
   PubMed Web of Science ®Google Scholar
• KangBKLeeJSChonSKDevelopment of self-microemulsifying drug delivery systems (SMEDDS) for oral bioavailability enhancement of simvastatin in beagle dogsInt J Pharm2004274657315072783
   PubMed Web of Science ®Google Scholar
• ShaXYYanGJWuYJLiJCFangXLEffect of self-microemulsifying drug delivery systems containing Labrasol on tight junctions in Caco-2 cellsEur J Pharm Sci20052447748615784337
   PubMed Web of Science ®Google Scholar
• KommuruTRGurleyBKhanMAReddyIKSelf-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessmentInt J Pharm200121223324611165081
   PubMed Web of Science ®Google Scholar
• SpernathAYaghmurAAserinAHoffmanREGartiNSelf-diffusion nuclear magnetic resonance, microstructure transitions, and solubilization capacity of phytosterols and cholesterol in Winsor IV food-grade microemulsionsJ Agric Food Chem2003512359236412670181
   PubMed Web of Science ®Google Scholar
• SpernathAYaghmurAAserinAHoffmanREGartiNFood-grade microemulsions based on nonionic emulsifiers: media to enhance lycopene solubilizationJ Agric Food Chem2002506917692212405797
   PubMed Web of Science ®Google Scholar
• AmarIAserinAGartiNSolubilization patterns of lutein and lutein esters in food grade nonionic microemulsionsJ Agric Food Chem2003514775478114705912
   PubMed Web of Science ®Google Scholar
• GartiNAmarIYaghmurASpernathAAserinAInterfacial modification and structural transitions induced by guest molecules solubilized in U-type nonionic microemulsionsJ Disper Sci Technol200324397410
   Web of Science ®Google Scholar
• GartiNAvrahamiMAserinAImproved solubilization of celecoxib in U-type nonionic microemulsions and their structural transitions with progressive aqueous dilutionJ Colloid Interface Sci200629935236516529763
   PubMed Web of Science ®Google Scholar
• KeWTLinSYHoHOSheuMTPhysical characterizations of microemulsion systems using tocopheryl polyethylene glycol 1000 succinate (TPGS) as a surfactant for the oral delivery of protein drugsJ Control Release200510248950715653166
   PubMed Web of Science ®Google Scholar
• PoutonCWFormulation of self-emulsifying drug delivery systemsAdv Drug Deliv Rev1997254758
   Web of Science ®Google Scholar
• HolmRPorterCJEdwardsGAMüllertzAKristensenHGCharmanWNExamination 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 triglyceridesEur J Pharm Sci200320919713678797
   PubMed Web of Science ®Google Scholar
• KhooSMHumberstoneAJPorterCJEdwardsGACharmanWNFormulation design and bioavailability assessment of lipidic self-emulsifying formulations of halofantrineInt J Pharm1998167155164
   Web of Science ®Google Scholar
• FrimanSBackmanLA new microemulsion formulation of cyclosporine: pharmacokinetic and clinical featuresClin Pharmacokinet1996301811938882300
   PubMed Web of Science ®Google Scholar
• KimJYKuYSEnhanced absorption of indomethacin after oral or rectal administration of a self-emulsifying system containing indomethacin in ratsInt J Pharm2000194818910601687
   PubMed Web of Science ®Google Scholar
• ShenHRZhongMKPreparation and evaluation of self-emulsifying drug delivery systems (SMEDDS) containing atorvastatinJ Pharm Pharmacol2006581183119116945176
   PubMed Web of Science ®Google Scholar
• GroveMMüllertzANielsenJLPedersenGPBioavailability of seocalcitol II: development and characterization of self-microemulsifying drug delivery systems (SMEDDS) for oral administration containing medium and long chain triglyceridesEur J Pharm Sci20062823324216650738
   PubMed Web of Science ®Google Scholar
• ChenYLiGWuXGSelf-microemulsifying drug delivery system (SMEDDS) of vinpocetine: formulation development and in vivo assessmentBiol Pharm Bull20083111812518175953
   PubMed Web of Science ®Google Scholar
• WooJSSongYKHongJYLimSJKimCKReduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteersEur J Pharm Sci20083315916518178070
   PubMed Web of Science ®Google Scholar
• FatourosDGNielsenFSDouroumisDHadjileontiadisLJMullertzAIn vitro-in vivo correlations of self-emulsifying drug delivery systems combining the dynamic lipolysis model and neuro-fuzzy networksEur J Pharm Biopharm20086988789818367386
   PubMed Web of Science ®Google Scholar
• ZhangPLiuYFengNPXuJPreparation and evaluation of self-emulsifying drug delivery system for oridoninInt J Pharm200835526927618242895
   PubMed Web of Science ®Google Scholar
• CooneyGFJeevanandamVChoudhurySFeutrenGMullerEAEisenHJComparative bioavailability of Neoral and Sandimmune in cardiac transplant recipients over 1 yearTransplant19983018921894
   Web of Science ®Google Scholar
• PorterCJCharmanWNIn vitro assessment of oral lipid based formulationsAdv Drug Deliv Rev200150Suppl 1S12714711576699
   PubMed Web of Science ®Google Scholar
• SubramanianNRaySGhosalSKBhadraRMoulikSPFormulation design of self-emulsifying drug delivery systems for improved oral bioavailability of CelecoxibBiol Pharm Bull2004271993199915577219
   PubMed Web of Science ®Google Scholar
• ParkKMKimCKPreparation and evaluation of flurbiprofen-loaded microemulsion for parenteral deliveryInt J Pharm199918117317910370213
   PubMed Web of Science ®Google Scholar
• MunozAGuichardJPReginaultPMicronisedFFBAtherosclerosis1994110SupplS45S487857384
   PubMed Web of Science ®Google Scholar
• StammASethPFenofibrate pharmaceutical composition having high bioavailability and method for preparing itUnited States patent US 6589552782003
   Google Scholar
• GuichardJPBlouquinPQingYA new formulation of FFB: suprabioavailable tabletsCurr Med Res Opin20001613413810893657
   PubMed Web of Science ®Google Scholar
• NajibJFFB in the treatment of dyslipidemia: a review of the data as they relate to the new suprabioavailable tablet formulationClin Ther2002242022205012581543
   PubMed Web of Science ®Google Scholar
• SonetBVanderbistFStreelBHouinGRandomized crossover studies of the bioequivalence of two FFB formulations after administration of a single oral dose in healthy volunteersArzneim Forsch20025220020411963648
   PubMed Web of Science ®Google Scholar
• PatelARVaviaPRPreparation and in vivo evaluation of SMEDDS (self-emulsifying drug delivery system) containing fenofibrateAAPS J200793E34435218170981
   PubMed Web of Science ®Google Scholar
• WangGMChenCHKeWTHoHOSheuMTCharacterizations of fenofibrate dissolution delivered by a self-microemulsifying drug delivery systemJ Pharm Pharmacol2010621685169621054394
   PubMed Web of Science ®Google Scholar