Comparative study on solid self-nanoemulsifying drug delivery and solid dispersion system for enhanced solubility and bioavailability of ezetimibe

References

• CladerJWThe discovery of ezetimibe: a view from outside the receptorJ Med Chem200441914695813
   PubMedGoogle Scholar
• BashaSJNaveedSATiwariNKConcurrent determination of ezetimibe and its phase-I and II metabolites by HPLC with UV detection: quantitative application to various in vitro metabolic stability studies and for qualitative estimation in bileJ Chromatogr B Analyt Technol Biomed Life Sci20078538896
   PubMed Web of Science ®Google Scholar
• KaranamSRKatakamPChanduBRHwisaNTAdikiSKSimultaneous determination of ezetimibe and simvastatin in rat plasma by stable-isotope dilution LC-ESI–MS/MS and its application to a pharmacokinetic studyJ Pharm Anal20134286294
   Google Scholar
• GulsunTGursoyRNOnerLDesign and characterization of nanocrystal formulations containing ezetimibeChem Pharm Bull (Tokyo)201159414521212545
   PubMed Web of Science ®Google Scholar
• PatelRBhimaniDPatelJPatelDSolid-state characterization and dissolution properties of ezetimibe–cyclodextrins inclusion complexesJ Incl Phenom Macrocycl Chem200860241251
   Web of Science ®Google Scholar
• EzzetFKrishnaGWexlerDBStatkevichPKosoglouTBatraVKA population pharmacokinetic model that describes multiple peaks due to enterohepatic recirculation of ezetimibeClin Ther20012387188511440287
   PubMed Web of Science ®Google Scholar
• KosoglouTStatkevichPJohnson-LevonasAPaoliniJFBergmanAJAltonKBEzetimibe: a review of its metabolism, pharmacokinetics and drug interactionsClin Pharmacokinet20054446749415871634
   PubMed Web of Science ®Google Scholar
• MandawgadeSDSharmaSPathakSPatravaleVBDevelopment of SMEDDS using natural lipophile: application to β-artemether deliveryInt J Pharm200836217918318652886
   PubMed Web of Science ®Google Scholar
• BalakrishnanPLeeBJOhDHEnhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS)Eur J Pharm Biopharm20097253954519298857
   PubMed Web of Science ®Google Scholar
• PatelARVaviaPRPreparation and in vivo evaluation of SMEDDS (self-microemulsifying drug delivery system) containing fenofibrateAAPS J20079E344E35218170981
   PubMed Web of Science ®Google Scholar
• NazzalSKhanMAControlled release of a self-emulsifying formulation from a tablet dosage form: stability assessment and optimization of some processing parametersInt J Pharm200631511012116563673
   PubMed Web of Science ®Google Scholar
• BandyopadhyaySKatareOSinghBDevelopment of optimized supersaturable self-nanoemulsifying systems of ezetimibe: effect of polymers and efflux transportersExpert Opin Drug Deliv20141147949224386966
   PubMed Web of Science ®Google Scholar
• TangBChengGGuJCXuCHDevelopment of solid self-emulsifying drug delivery systems: preparation techniques and dosage formsDrug Discov Today20081360661218598917
   PubMed Web of Science ®Google Scholar
• YanYDSungJHKimKKNovel valsartan-loaded solid dispersion with enhanced bioavailability and no crystalline changesInt J Pharm201242220221022085435
   PubMed Web of Science ®Google Scholar
• OhDHParkYJKangJHYongCSChoiHGPhysicochemical characterization and in vivo evaluation of flurbiprofen-loaded solid dispersion without crystalline changeDrug Deliv201118465320726805
   PubMed Web of Science ®Google Scholar
• RashidRKimDWDinFUEffect of hydroxypropylcellulose and Tween 80 on physicochemical properties and bioavailability of ezetimibe-loaded solid dispersionCarbohydr Polym2015130263126076597
   PubMed Web of Science ®Google Scholar
• ParkYJRyuDSLiDXPhysicochemical characterization of tacrolimus-loaded solid dispersion with sodium carboxylmethyl cellulose and sodium lauryl sulfateArch Pharm Res20093289389819557367
   PubMed Web of Science ®Google Scholar
• TranTHPoudelBKMarasiniNPreparation and evaluation of raloxifene-loaded solid dispersion nanoparticle by spray drying technique without an organic solventInt J Pharm201344505723318367
   PubMed Web of Science ®Google Scholar
• BaeJWChoiCIParkSHJangCGLeeSYAnalytical LC-MS/MS method for ezetimibe and its application for pharmacokinetic studyJ Liq Chromatogr Relat Technol201235141152
   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
• SinghAKChaurasiyaASinghMUpadhyaySCMukherjeeRKharRKExemestane loaded self-microemulsifying drug delivery system (SMEDDS): development and optimizationAAPS Pharm Sci Tech20089628634
   PubMed Web of Science ®Google Scholar
• PoutonCWLipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and ‘self-microemulsifying’ drug delivery systemsEur J Pharm Sci200011S93S9811033431
   PubMed Web of Science ®Google Scholar
• BalakrishnanPLeeBJOhDHEnhanced oral bioavailability of Coenzyme Q10 by self-emulsifying drug delivery systemsInt J Pharm2009374667219446761
   PubMed Web of Science ®Google Scholar
• ConstantinidesPPScalartJPLancasterCFormulation and intestinal absorption enhancement evaluation of water-in-oil microemulsions incorporating medium-chain glyceridesPharma Res19941113851390
   Google Scholar
• BandyopadhyaySKatareOSinghBOptimized self nano-emulsifying systems of ezetimibe with enhanced bioavailability potential using long chain and medium chain triglyceridesColloids Surf B Biointerfaces2012100506122766282
   PubMed Web of Science ®Google Scholar
• LewisRJSax’s Dangerous Properties of Industrial Materials11th edNew York, NYWiley20042013
   Google Scholar
• ChoHJParkJWYoonISKimDDSurface-modified solid lipid nanoparticles for oral delivery of docetaxel: enhanced intestinal absorption and lymphatic uptakeInt J Nanomedicine2014949550424531717
   PubMed Web of Science ®Google Scholar
• DannenfelserRMHeHJoshiYBatemanSSerajuddinADevelopment of clinical dosage forms for a poorly water soluble drug I: application of polyethylene glycol–polysorbate 80 solid dispersion carrier systemJ Pharm Sci2004931165117515067693
   PubMed Web of Science ®Google Scholar
• LeeSNPoudelBKTranTHA novel surface-attached carvedilol solid dispersion with enhanced solubility and dissolutionArch Pharm Res201336798523328872
   PubMed Web of Science ®Google Scholar
• SethiaSSquillanteESolid dispersion of carbamazepine in PVP K30 by conventional solvent evaporation and supercritical methodsInt J Pharm200427211015019063
   PubMed Web of Science ®Google Scholar
• JoeJHLeeWMParkYJEffect of the solid-dispersion method on the solubility and crystalline property of tacrolimusInt J Pharm201039516116620580799
   PubMed Web of Science ®Google Scholar
• WangXMichoelAVan den MooterGSolid state characteristics of ternary solid dispersions composed of PVP VA64, Myrj 52 and itraconazoleInt J Pharm2005303546116105723
   PubMed Web of Science ®Google Scholar
• NewaMBhandariKHLiDXPreparation, characterization and in vivo evaluation of ibuprofen binary solid dispersions with poloxamer 188Int J Pharm200734322823717597315
   PubMed Web of Science ®Google Scholar
• SanchetiPKarekarPVyasVShahMPoreYPreparation and physicochemical characterization of surfactant based solid dispersions of ezetimibePharmazie20096422723119435139
   PubMed Web of Science ®Google Scholar
• BaliVAliMAliJStudy of surfactant combinations and development of a novel nanoemulsion for minimising variations in bioavailability of ezetimibeColloids Surf B Biointerfaces20107641042020042320
   PubMed Web of Science ®Google Scholar
• Ming ThauSChing MinYSokoloskiTDCharacterization and dissolution of fenofibrate solid dispersion systemsInt J Pharm1994103137146
   Google Scholar
• KimDWKwonMSYousafAMComparison of a solid SMEDDS and solid dispersion for enhanced stability and bioavailability of clopidogrel napadisilateCarbohydr Polym201411436537425263903
   PubMed Web of Science ®Google Scholar
• ZhangPLiuYFengNXuJPreparation and evaluation of self-microemulsifying drug delivery system of oridoninInt J Pharm200835526927618242895
   PubMed Web of Science ®Google Scholar
• GelderblomHVerweijJvan ZomerenDMInfluence of Cremophor EL on the bioavailability of intraperitoneal paclitaxelClin Cancer Res2002841237124111948138
   PubMed Web of Science ®Google Scholar
• WoodcockDMJeffersonSLinsenmeyerMEReversal of the multidrug resistance phenotype with cremophor EL, a common vehicle for water-insoluble vitamins and drugsCancer Res199050419942032364376
   PubMed Web of Science ®Google Scholar
• SchuurhuisGBroxtermanHPinedoHThe polyoxyethylene castor oil Cremophor EL modifies multidrug resistanceBr J Cancer1990625912223576
   PubMedGoogle Scholar
• RossDDWootenPJTongYSynergistic reversal of multidrug-resistance phenotype in acute myeloid leukemia cells by cyclosporin A and cremophor ELBlood199483133713478118035
   PubMed Web of Science ®Google Scholar
• SykesEWoodburnKDeckerDKesselDEffects of Cremophor EL on distribution of Taxol to serum lipoproteinsBr J Cancer1994704014047915910
   PubMed Web of Science ®Google Scholar
• WoodburnKChangCLeeSHendersonBKesselDBiodistribution and PDT efficacy of a ketochlorin photosensitizer as a function of the delivery vehiclePhotochem Photobiol1994601541597938213
   PubMed Web of Science ®Google Scholar