Engineering of solidified glyburide nanocrystals for tablet formulation via loading of carriers: downstream processing, characterization, and bioavailability

References

• FuQLiBZhangDComparative studies of the in vitro dissolution and in vivo pharmacokinetics for different formulation strategies (solid dispersion, micronization, and nanocrystals) for poorly water-soluble drugs: a case study for lacidipineColloids Surf B: Biointerf2015132Supplement C171176
   PubMedGoogle Scholar
• JinnoJKamadaNMiyakeMEffect of particle size reduction on dissolution and oral absorption of a poorly water-soluble drug, cilostazol, in beagle dogsJ Control Release20061111–2566416410029
   PubMed Web of Science ®Google Scholar
• SalazarJGhanemAMüllerRHMöschwitzerJPNanocrystals: comparison of the size reduction effectiveness of a novel combinative method with conventional top-down approachesEur J Pharm Biopharm2012811829022233547
   PubMed Web of Science ®Google Scholar
• JunghannsJUMüllerRHNanocrystal technology, drug delivery and clinical applicationsInt J Nanomed200833295310
   PubMed Web of Science ®Google Scholar
• AssadpourEJafariSMA systematic review on nanoencapsulation of food bioactive ingredients and nutraceuticals by various nanocarriersCrit Rev Food Sci Nutr201863123
   Google Scholar
• GadadareRMandpeLPokharkarVUltra rapidly dissolving repaglinide nanosized crystals prepared via bottom-up and top-down approach: influence of food on pharmacokinetics behaviorAAPS PharmSciTech201516478779925549790
   PubMed Web of Science ®Google Scholar
• RomeroGBBryschWKeckCMMüllerRHNanocapsule formation by nanocrystalsJafariSMNanoencapsulation Technologies for the Food and Nutraceutical IndustriesCambridge, MAAcademic Press2017165186
   Google Scholar
• Raghava SrivalliKMMishraBDrug nanocrystals: a way toward scale-upSaudi Pharm J201624438640427330370
   PubMedGoogle Scholar
• MüllerRHGohlaSKeckCMState of the art of nanocrystals – special features, production, nanotoxicology aspects and intracellular deliveryEur J Pharm Biopharm20117811921266197
   PubMed Web of Science ®Google Scholar
• MüllerRHShegokarRKeckCM20 years of lipid nanoparticles (SLN and NLC): present state of development and industrial applicationsCurr Drug Discov Technol20118320722721291409
   PubMedGoogle Scholar
• PawarVKSinghYMeherJGGuptaSChourasiaMKEngineered nanocrystal technology: in-vivo fate, targeting and applications in drug deliveryJ Control Release2014183Supplement C516624667572
   PubMedGoogle Scholar
• WuLZhangJWatanabeWPhysical and chemical stability of drug nanoparticlesAdv Drug Deliv Rev201163645646921315781
   PubMed Web of Science ®Google Scholar
• D’AddioSMPrud’hommeRKControlling drug nanoparticle formation by rapid precipitationAdv Drug Deliv Rev201163641742621565233
   PubMed Web of Science ®Google Scholar
• RabinowBENanosuspensions in drug deliveryNat Rev Drug Discov20043978579615340388
   PubMed Web of Science ®Google Scholar
• ArpagausCCollenbergARüttiDAssadpourEJafariSMNano spray drying for encapsulation of pharmaceuticalsInt J Pharm20185461–219421429778825
   PubMed Web of Science ®Google Scholar
• CalKSollohubKSpray drying technique. I: hardware and process parametersJ Pharm Sci201099257558619774644
   PubMed Web of Science ®Google Scholar
• WaltersRHBhatnagarBTchessalovSIzutsuKITsumotoKOhtakeSNext generation drying technologies for pharmaceutical applicationsJ Pharm Sci201410392673269524916125
   PubMed Web of Science ®Google Scholar
• HeWLuYQiJChenLYinLWuWFormulating food protein-stabilized indomethacin nanosuspensions into pellets by fluid-bed coating technology: physical characterization, redispersibility, and dissolutionInt J Nanomed2013831193128
   PubMed Web of Science ®Google Scholar
• TuomelaALaaksonenTLaruJSolid formulations by a nanocrystal approach: critical process parameters regarding scale-ability of nano-crystals for tableting applicationsInt J Pharm20154851–2778625746735
   PubMedGoogle Scholar
• YuLLiCLeYChenJ-FZouHStabilized amorphous glibenclamide nanoparticles by high-gravity techniqueMater Chem Phys20111301–2361366
   Google Scholar
• GuanJHanJZhangDIncreased dissolution rate and oral bioavailability of hydrophobic drug glyburide tablets produced using supercritical CO2 silica dispersion technologyEur J Pharm Biopharm201486337638224184803
   PubMed Web of Science ®Google Scholar
• WeiHLöbenbergRBiorelevant dissolution media as a predictive tool for glyburide a class II drugEur J Pharm Sci2006291455216815694
   PubMed Web of Science ®Google Scholar
• LiuHShangKLiuWImproved oral bioavailability of glyburide by a self-nanoemulsifying drug delivery systemJ Microencapsul201431327728324533514
   PubMed Web of Science ®Google Scholar
• BetageriGMakarlaKREnhancement of dissolution of glyburide by solid dispersion and lyophilization techniquesInt J Pharm19951261–2155160
   Web of Science ®Google Scholar
• SavolainenJJärvinenKTaipaleHJarhoPLoftssonTJärvinenTCo-administration of a water-soluble polymer increases the usefulness of cyclodextrins in solid oral dosage formsPharm Res19981511169617019833990
   PubMedGoogle Scholar
• NnamaniPOAttamaAAIbezimECAdikwuMUSRMS142-based solid lipid microparticles: application in oral delivery of glibenclamide to diabetic ratsEur J Pharm Biopharm2010761687420554020
   PubMed Web of Science ®Google Scholar
• ShahSRParikhRHChavdaJRShethNRApplication of Plackett– Burman screening design for preparing glibenclamide nanoparticles for dissolution enhancementPowder Technol2013235Supplement C405411
   Google Scholar
• GonçalvesLMMaestrelliFdi Cesare MannelliLGhelardiniCAlmeidaAJMuraPDevelopment of solid lipid nanoparticles as carriers for improving oral bioavailability of glibenclamideEur J Pharm Biopharm2016102Supplement C415026925503
   PubMedGoogle Scholar
• AliHSMHanafyAFGlibenclamide nanocrystals in a biodegradable chitosan patch for transdermal delivery: engineering, formulation, and evaluationJ Pharm Sci2017106140241027866687
   PubMed Web of Science ®Google Scholar
• ZhangXGuanJNiRLiLCMaoSPreparation and solidification of redispersible nanosuspensionsJ Pharm Sci201410372166217624840928
   PubMed Web of Science ®Google Scholar
• YuePFWanJWangYD-alpha-tocopherol acid polyethylene glycol 1000 succinate, an effective stabilizer during solidification transformation of baicalin nanosuspensionsInt J Pharm20134431–227928723291447
   PubMedGoogle Scholar
• OsamuraTTakeuchiYOnoderaRFormulation design of granules prepared by wet granulation method using a multi-functional single-punch tablet press to avoid tableting failuresAsian J Pharm Sci2018132113119
   PubMedGoogle Scholar
• JaipakdeeNLimpongsaESripanidkulchaiBOPiyachaturawatPPreparation of Curcuma comosa tablets using liquisolid techniques: in vitro and in vivo evaluationInt J Pharm20185531–215716830316793
   PubMedGoogle Scholar
• SalazarJMüllerRHMöschwitzerJPApplication of the combinative particle size reduction technology H 42 to produce fast dissolving glibenclamide tabletsEur J Pharm Sci201349456557723587645
   PubMedGoogle Scholar
• SallamNMSanadRAKharshoumRMZineldinMADevelopment of salbutamol sulphate fast disintegrating sublingual tablets with enhanced bioavailability and improved clinical efficacy for potential treatment of asthmaJ Drug Deliv Sci Technol2017417889
   Web of Science ®Google Scholar
• YangWWangYFuQThe role of particle size of glyburide crystals in improving its oral absorptionDrug Deliv Transl Res20177342843828364197
   PubMedGoogle Scholar
• LucioDIracheJMFontMMartínez-OhárrizMCSupramolecular structure of glibenclamide and β-cyclodextrins complexesInt J Pharm20175301–237738628779983
   PubMedGoogle Scholar
• ElbahwyIAIbrahimHMIsmaelHRKasemAAEnhancing bioavailability and controlling the release of glibenclamide from optimized solid lipid nanoparticlesJ Drug Deliv Sci Technol2017387889
   Web of Science ®Google Scholar
• MoghimiSMHunterACPoloxamers and poloxamines in nanoparticle engineering and experimental medicineTrends Biotechnol2000181041242010998507
   PubMed Web of Science ®Google Scholar
• LiuPViitalaTKartal-HodzicAInteraction studies between indomethacin nanocrystals and PEO/PPO copolymer stabilizersPharm Res201532262863925145336
   PubMedGoogle Scholar
• MorakulBSuksiriworapongJLeanpolchareanchaiJJunyaprasertVBPrecipitation-lyophilization-homogenization (PLH) for preparation of clarithromycin nanocrystals: influencing factors on physicochemical properties and stabilityInt J Pharm2013457118719624076396
   PubMedGoogle Scholar
• LucioDMartínez-OhárrizMCJarasGOptimization and evaluation of zein nanoparticles to improve the oral delivery of glibenclamide in vivo study using C. elegansEur J Pharm Biopharm201712110411228986295
   PubMedGoogle Scholar
• LeeHJLeeHGKwonYBThe role of lactose carrier on the powder behavior and aerodynamic performance of bosentan microparticles for dry powder inhalationEur J Pharm Sci201811727928929510172
   PubMed Web of Science ®Google Scholar
• EmamiJKazemaliMRDesign and in vitro evaluation of a novel controlled onset extended-release delivery system of metoprolol tartrateRes Pharm Sci2016111819227051436
   PubMedGoogle Scholar
• LaiSLGuoJYPetrovaVRamanathGAllenLHSize-dependent melting properties of small tin particles: nanocalorimetric measurementsPhys Rev Lett19967719910210061781
   PubMedGoogle Scholar
• MoolchandaniVAugsburgerLLGuptaAKhanMLangridgeJHoagSWCharacterization and selection of suitable grades of lactose as functional fillers for capsule filling: Part 1Drug Dev Ind Pharm20154191452146325212639
   PubMed Web of Science ®Google Scholar
• FuQLiBZhangDComparative studies of the in vitro dissolution and in vivo pharmacokinetics for different formulation strategies (solid dispersion, micronization, and nanocrystals) for poorly water-soluble drugs: a case study for lacidipineColloids Surf B Biointerfaces201513217117626047880
   PubMed Web of Science ®Google Scholar
• MöschwitzerJPMüllerRHFactors influencing the release kinetics of drug nanocrystal-loaded pellet formulationsDrug Dev Ind Pharm201339576276922803784
   PubMed Web of Science ®Google Scholar
• HengDOgawaKCutlerDJPure drug nanoparticles in tablets: what are the dissolution limitations?J Nanopart Res201012517431754
   Google Scholar
• HeCYinLTangCYinCSize-dependent absorption mechanism of polymeric nanoparticles for oral delivery of protein drugsBiomaterials201233338569857822906606
   PubMed Web of Science ®Google Scholar
• BaekIHKimJSHaESDissolution and oral absorption of pranlukast nanosuspensions stabilized by hydroxypropylmethyl celluloseInt J Biol Macromol201467535724631786
   PubMed Web of Science ®Google Scholar
• MuSLiMGuoMSpironolactone nanocrystals for oral administration: different pharmacokinetic performances induced by stabilizersColloids Surf B Biointerfaces2016147738027490456
   PubMed Web of Science ®Google Scholar
• JiangTHanNZhaoBXieYWangSEnhanced dissolution rate and oral bioavailability of simvastatin nanocrystal prepared by sono-precipitationDrug Dev Ind Pharm201238101230123922229827
   PubMed Web of Science ®Google Scholar