Solid self-nanoemulsifying cyclosporin A pellets prepared by fluid-bed coating: preparation, characterization and in vitro redispersibility

References

• LipinskiCAPoor aqueous solubility – an industry wide problem in drug discoveryAm Pharm Rev200258285
   Google Scholar
• DressmanJReppasCDrug solubility: How to measure it, how to improve itAdv Drug Deliv Rev200759531532
   Web of Science ®Google Scholar
• PoutonCWPorterCJHFormulation of lipid-based delivery systems for oral administration: Materials, methods and strategiesAdv Drug Deliv Rev20086062563718068260
   PubMed Web of Science ®Google Scholar
• CuiJYuBZhaoYEnhancement of oral absorption of curcumin by self-microemulsifying drug delivery systemsInt J Pharm200937114815519124065
   PubMed Web of Science ®Google Scholar
• WooJSSongYKHongJYReduced food-effect and enhanced bioavailability of a self-microemulsifying formulation of itraconazole in healthy volunteersEur J Pharm Sci20083315916518178070
   PubMed Web of Science ®Google Scholar
• ZvonarABergincKKristlAMicroencapsulation of self-microemulsifying system: Improving solubility and permeability of furosemideInt J Pharm201038815115820060454
   PubMed Web of Science ®Google Scholar
• NazzalSKhanMAResponse surface methodology for the optimization of ubiquinone self-emulsified drug delivery systemAAPS Pharm Sci Tech200231E3
   Google Scholar
• NazzalSSmalyukhIILavrentovichODPreparation and in-vitro characterization of a eutectic based semisolid self nanoemulsified drug delivery system (SNEDDS) of ubiquinone: Mechanism and progress of emulsion formationInt J Pharm200223524726511879759
   PubMed Web of Science ®Google Scholar
• NazzalSNutanMPalamakulaAOptimization of a self-nanoemulsified tablet dosage form of ubiquinone using response surface methodology: Effect of formulation ingredientsInt J Pharm200224010311412062506
   PubMed Web of Science ®Google Scholar
• NazzalSZaghloulAAKhanMAEffect of extragranular microcrystalline cellulose on compaction, surface roughness and in-vitro dissolution of a self-nanoemulsified solid dosage form of ubiquinonePharm Technol2002268698
   Google Scholar
• DixitRPNagarsenkerMSSelf-nanoemulsifying granules of ezetimibe: Design, optimization and evaluationEur J Pharm Sci20083518319218652892
   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
• ItoYKusawakeTIshidaMOral solid gentamicin preparation using emulsifier and adsorbentJ Control Release2005105233115908031
   PubMed Web of Science ®Google Scholar
• SanderCHolmPPorous magnesium aluminometasilicate tablets as carrier of a cyclosporine self-emulsifying formulationAAPS Pharm Sci Tech20091013881395
   PubMed Web of Science ®Google Scholar
• BoltriLCoceaniNDe CurtoDEnhancement and modification of etoposide release from crosspovidone particles loaded with oil-surfactant blendsPharm Dev Technol199723733819552466
   PubMedGoogle 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
• YiTWangJXuHA new solid-microemulsifying formulation prepared by spray-drying to improve the oral bioavailability of poorly water soluble drugsEur J Pharm Biopharm20087043944418603415
   PubMed Web of Science ®Google Scholar
• HomarMŠuligojDGašperlinMPreparation of microcapsules with self-microemulsifing core by a vibrating nozzle methodJ Microencapsul200724728117438943
   PubMed Web of Science ®Google Scholar
• WangZSunJWangYSolid self-emulsifying nitrendipine pellets: Preparation and in vitro/in vivo evaluationInt J Pharm20103831619698771
   PubMed Web of Science ®Google Scholar
• AbdallaAKleinSMäderKA new self-emulsifying drug delivery system (SEDDS) for poorly soluble drugs: Characterization, dissolution, in vitro digestion and incorporation into solid pelletsEur J Pharm Sci20083545746418940249
   PubMed Web of Science ®Google Scholar
• AbdallaAMäderKPreparation and characterization of a self-emulsifying pellet formulationEur J Pharm Biopharm20076622022617196807
   PubMed Web of Science ®Google Scholar
• SerratoniMNewtonMBoothSControlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying systemEur J Pharm Biopharm200765949817056237
   PubMed Web of Science ®Google Scholar
• NewtonMPeterssonJPodczeckFThe influence of formulation variables on the properties of pellets containing a self-emulsifying mixtureJ Pharm Sci20019098799511536202
   PubMed Web of Science ®Google Scholar
• SunNWeiXWuBEnhanced dissolution of silymarin/polyvinylpyrrolidone solid dispersion pellets prepared by a one-step fluid-bed coating techniquePowder Technology20081827280
   Web of Science ®Google Scholar
• ZhangXSunNWuBPhysical characterization of lansoprazole/PVP solid dispersion prepared by fluid-bed coating techniquePowder Technology2008182480485
   Web of Science ®Google Scholar
• ZhangXWuDLaiJPiroxicam/2-hydroxypropyl-beta-cyclodextrin inclusion complex prepared by a new fluid-bed coating techniqueJ Pharm Sci20099866567518543294
   PubMed Web of Science ®Google Scholar
• WangYWuWQueLInvestigation on oil/Tween80/alcohol/water system pseudo-ternary phase diagrams and self-microemulsifying drug delivery systemChin J Pharm200536345348
   Google Scholar
• PatelARVaviaPRPreparation and in vivo evaluation of SMEDDS (self-microemulsifying drug delivery system) containing fenofibrateAAPS J20079E344E35218170981
   PubMed Web of Science ®Google Scholar
• LaiJLuYYinZPharmacokinetics and enhanced oral bioavailability in beagle dogs of cyclosporine A encapsulated in glyceryl monooleate/poloxamer 407 cubic nanoparticlesInt J Nanomedicine20105132320161984
   PubMed Web of Science ®Google Scholar
• IdeJNägeleAEwaldSEudragit^® Application Guidelines10th edParsippany, NJDegussa Corporation2007
   Google Scholar
• LuYZhangXLaiJPhysical characterization of meloxicam-β-cyclodextrin inclusion complex pellets prepared by a fluid-bed coating methodParticuology2009718
   Web of Science ®Google Scholar
• MüllerRHRungeSARavelliVCyclosporine-loaded solid lipid nanoparticles (SLN®): Drug-lipid physicochemical interactions and characterization of drug incorporationEur J Pharm Biopharm20086853554417804210
   PubMed Web of Science ®Google Scholar