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Original Research

Development and optimization of a self-microemulsifying drug delivery system for ator vastatin calcium by using d-optimal mixture design

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Pages 3865-3878 | Published online: 05 Jun 2015

References

  • HeJGuDReynoldsKSerum total and lipoprotein cholesterol levels and awareness, treatment, and control of hypercholesterolemia in ChinaCirculation2004110440541115238453
  • VaculikovaEGrunwaldovaVKralVDohnalJJampilekJPreparation of candesartan and atorvastatin nanoparticles by solvent evaporationMolecules20121711132211323423132139
  • WuXWhitfieldLRStewartBHAtorvastatin transport in the Caco-2 cell model: contributions of P-glycoprotein and the proton-monocarboxylic acid co-transporterPharm Res200017220921510751037
  • LennernäsHClinical pharmacokinetics of atorvastatinClin Pharmacokinet200342131141116014531725
  • ArunkumarNDeecaramanMRaniCMohanrajKPVenkates KumarKPreparation and solid state characterization of atorvastatin nanosuspensions for enhanced solubility and dissolutionInt J Pharm Tech Res20091417251730
  • AnwarMWarsiMHMallickNEnhanced bioavailability of nano-sized chitosan–atorvastatin conjugate after oral administration to ratsEur J Pharm Sci201144324124921864678
  • AyalonALevingerMRoytblatSNiddamVLifshitzRAronhimeJPolymorphic form of atorvastatin calciumUnited States Patent US 7,411,075882008
  • ChoudharyARanaACAggarwalGKumarVZakirFDevelopment and characterization of an atorvastatin solid dispersion formulation using skimmed milk for improved oral bioavailabilityActa Pharm Sin B201224421428
  • PalemCRPatelSPokharkarVBSolubility and stability enhancement of atorvastatin by cyclodextrin complexationPDA J Pharm Sci Technol200963321722520069794
  • ZhangHXWangJXZhangZBLeYShenZGChenJFMicronization of atorvastatin calcium by antisolvent precipitation processInt J Pharm2009374110611319446766
  • JinSKChoWKParkHJDevelopment of self-microemulsifying drug delivery system for enhancing the bioavailability of atorvastatinJ Pharm Invest2011412103109
  • SongWHParkJHYeomDWEnhanced dissolution of celecoxib by supersaturating self-emulsifying drug delivery system (S-SEDDS) formulationArch Pharm Res2013361697823325487
  • BandivadekaMMPancholiSSKaul-GhanekarRChoudhariAKoppikarSSelf-microemulsifying smaller molecular volume oil (Capmul MCM) using non-ionic surfactants: a delivery system for poorly water-soluble drugDrug Dev Ind Pharm201238788389222087760
  • ConstantinidesPPLipid microemulsions for improving drug dissolution and oral absorption: physical and biopharmaceutical aspectsPharm Res19951211156115728592652
  • SongWHYeomDWLeeDHIn situ intestinal permeability and in vivo oral bioavailability of celecoxib in supersaturating self-emulsifying drug delivery systemArch Pharm Res201437562663523852645
  • PorterCJCharmanWNIn vitro assessment of oral lipid based formulationsAdv Drug Deliv Rev200150Suppl 1S127S14711576699
  • ThiTDVan SpeybroeckMBarillaroVFormulate-ability of ten compounds with different physicochemical profiles in SMEDDSEur J Pharm Sci200938547948819782131
  • LiuYZhangPFengNZhangXWuSZhaoJOptimization and in situ intestinal absorption of self-microemulsifying drug delivery system of oridoninInt J Pharm2009365113614218782611
  • MarasiniNYanYDPoudelBKChoiHGYongCSKimJODevelopment and optimization of self-nanoemulsifying drug delivery system with enhanced bioavailability by Box-Behnken design and desirability functionJ Pharm Sci2012101124584459623023800
  • HolmRJensenIHSonnergaardJOptimization of self-microemulsifying drug delivery systems (SMEDDS) using a D-optimal design and the desirability functionDrug Dev Ind Pharm20063291025103217012115
  • MukherjeeTPlakogiannisFMDevelopment and oral bioavailability assessment of a supersaturated self-microemulsifying drug delivery system (SMEDDS) of albendazoleJ Pharm Pharmacol20106291112112020796189
  • MuraPFurlanettoSCirriMMaestrelliFMarrasAMPinzautiSOptimization of glibenclamide tablet composition through the combined use of differential scanning calorimetry and D-optimal mixture experimental designJ Pharm Biomed Anal2005371657115664744
  • BorhadeVNairHHegdeDDesign and evaluation of self-microemulsifying drug delivery system (SMEDDS) of tacrolimusAAPS Pharm Sci Tech2008911321
  • PoutonCWLipid formulations for oral administration of drugs: non-emulsifying, self-emulsifying and ‘self-microemulsifying’drug delivery systemsEur J Pharm Sci200011Suppl 2S93S9811033431
  • JanninVMusakhanianJMarchaudDApproaches for the development of solid and semi-solid lipid-based formulationsAdv Drug Deliv Rev200860673474618045728
  • LiLYiTLamCWInteractions between human multidrug resistance related protein (MRP2; ABCC2) and excipients commonly used in self-emulsifying drug delivery systems (SEDDS)Int J Pharm2013447119219823462368
  • DixitARRajputSJPatelSGPreparation and bioavailability assessment of SMEDDS containing valsartanAAPS Pharm Sci Tech2010111314321
  • GuptaSChavhanSSawantKKSelf-nanoemulsifying drug delivery system for adefovir dipivoxil: design, characterization, in vitro and ex vivo evaluationColloids Surf A Physicochem Eng Asp20113921145155
  • CuiSXNieSFLiLWangCGPanWSSunJPPreparation and evaluation of self-microemulsifying drug delivery system containing vinpocetineDrug Dev Ind Pharm200935560361119040178
  • MalcolmsonCSatraCKantariaSSidhuALawrenceMJEffect of the nature of oil on the incorporation of testosterone propionate into nonionic oil-in-water microemulsionsJ Pharm Sci19988711091169452978
  • WarisnoicharoenWLansleyABLawrenceMJNonionic oil in-water microemulsions: the effect of oil type on phase behaviourInt J Pharm2000198172710722947
  • DressmanJBReppasCIn vitro-in vivo correlations for lipophilic, poorly water soluble drugsEur J Pharm Sci200011Suppl 2S73S8011033429
  • AtiklerUDemirHTokatlıFTıhmınlıoğluFBalköseDÜlküSOptimisation of the effect of colemanite as a new synergistic agent in an intumescent systemPolym Degrad Stab200691715631570
  • BalakrishnanPLeeBJOhDHEnhanced oral bioavailability of coenzyme Q10 by self-emulsifying drug delivery systemsInt J Pharm20093741667219446761
  • AkhterSJainGKAhmadFJInvestigation of nanoemulsion system for transdermal delivery of domperidone: ex-vivo and in vivo studiesCurr Nanosci200844381390
  • AttamaAANkemneleMOIn vitro evaluation of drug release from self micro-emulsifying drug delivery systems using a biodegradable homolipid from Capra hircusInt J Pharm2005304141016198521
  • GroveMMüllertzAPedersenGPNielsenJLBioavailability of seocalcitol: III. Administration of lipid-based formulations to minipigs in the fasted and fed stateEur J Pharm Sci200731181517383165
  • ShenHZhongMPreparation and evaluation of self-microemulsifying drug delivery systems (SMEDDS) containing atorvastatinJ Pharm Pharmacol20065891183119116945176