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Journal Abstract Search

328 related items for PubMed ID: 24585389

  • 1. Lyophilized silica lipid hybrid (SLH) carriers for poorly water-soluble drugs: physicochemical and in vitro pharmaceutical investigations.
    Yasmin R, Tan A, Bremmell KE, Prestidge CA.
    J Pharm Sci; 2014 Sep; 103(9):2950-2959. PubMed ID: 24585389
    [Abstract] [Full Text] [Related]

  • 2. Pluronic-Functionalized Silica-Lipid Hybrid Microparticles: Improving the Oral Delivery of Poorly Water-Soluble Weak Bases.
    Rao S, Richter K, Nguyen TH, Boyd BJ, Porter CJ, Tan A, Prestidge CA.
    Mol Pharm; 2015 Dec 07; 12(12):4424-33. PubMed ID: 26523928
    [Abstract] [Full Text] [Related]

  • 3. Silica encapsulated lipid-based drug delivery systems for reducing the fed/fasted variations of ziprasidone in vitro.
    Dening TJ, Rao S, Thomas N, Prestidge CA.
    Eur J Pharm Biopharm; 2016 Apr 07; 101():33-42. PubMed ID: 26812284
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  • 4. Nanocrystal-silica-lipid hybrid particles for the improved oral delivery of ziprasidone in vitro.
    Meola TR, Dening TJ, Prestidge CA.
    Eur J Pharm Biopharm; 2018 Aug 07; 129():145-153. PubMed ID: 29857135
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  • 5. Silica-lipid hybrid (SLH) microcapsules: a novel oral delivery system for poorly soluble drugs.
    Tan A, Simovic S, Davey AK, Rades T, Prestidge CA.
    J Control Release; 2009 Feb 20; 134(1):62-70. PubMed ID: 19013488
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  • 6. Silica nanoparticles to control the lipase-mediated digestion of lipid-based oral delivery systems.
    Tan A, Simovic S, Davey AK, Rades T, Boyd BJ, Prestidge CA.
    Mol Pharm; 2010 Apr 05; 7(2):522-32. PubMed ID: 20063867
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  • 8. Dry hybrid lipid-silica microcapsules engineered from submicron lipid droplets and nanoparticles as a novel delivery system for poorly soluble drugs.
    Simovic S, Heard P, Hui H, Song Y, Peddie F, Davey AK, Lewis A, Rades T, Prestidge CA.
    Mol Pharm; 2009 Apr 05; 6(3):861-72. PubMed ID: 19358600
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  • 10. Silica-lipid hybrid (SLH) versus non-lipid formulations for optimising the dose-dependent oral absorption of celecoxib.
    Tan A, Davey AK, Prestidge CA.
    Pharm Res; 2011 Sep 05; 28(9):2273-87. PubMed ID: 21560021
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  • 11. Porous Silica-Supported Solid Lipid Particles for Enhanced Solubilization of Poorly Soluble Drugs.
    Yasmin R, Rao S, Bremmell KE, Prestidge CA.
    AAPS J; 2016 Jul 05; 18(4):876-85. PubMed ID: 27048207
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  • 13. Synergistic role of solid lipid and porous silica in improving the oral delivery of weakly basic poorly water soluble drugs.
    Yasmin R, Rao S, Bremmell K, Prestidge C.
    Eur J Pharm Sci; 2017 Jan 01; 96():508-514. PubMed ID: 27793717
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  • 14. Enhancing the oral bioavailability of simvastatin with silica-lipid hybrid particles: The effect of supersaturation and silica geometry.
    Meola TR, Schultz HB, Peressin KF, Prestidge CA.
    Eur J Pharm Sci; 2020 Jul 01; 150():105357. PubMed ID: 32446169
    [Abstract] [Full Text] [Related]

  • 15. Exploitation of 3D face-centered cubic mesoporous silica as a carrier for a poorly water soluble drug: influence of pore size on release rate.
    Zhu W, Wan L, Zhang C, Gao Y, Zheng X, Jiang T, Wang S.
    Mater Sci Eng C Mater Biol Appl; 2014 Jan 01; 34():78-85. PubMed ID: 24268236
    [Abstract] [Full Text] [Related]

  • 16. An oral delivery system for indomethicin engineered from cationic lipid emulsions and silica nanoparticles.
    Simovic S, Hui H, Song Y, Davey AK, Rades T, Prestidge CA.
    J Control Release; 2010 May 10; 143(3):367-73. PubMed ID: 20079390
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