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Journal Abstract Search

349 related items for PubMed ID: 19056493

  • 1. Computer simulations using GastroPlus to justify a biowaiver for etoricoxib solid oral drug products.
    Okumu A, DiMaso M, Löbenberg R.
    Eur J Pharm Biopharm; 2009 May; 72(1):91-8. PubMed ID: 19056493
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  • 2. Application of absorption modeling to predict bioequivalence outcome of two batches of etoricoxib tablets.
    Mitra A, Kesisoglou F, Dogterom P.
    AAPS PharmSciTech; 2015 Feb; 16(1):76-84. PubMed ID: 25182387
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  • 3. Dynamic dissolution testing to establish in vitro/in vivo correlations for montelukast sodium, a poorly soluble drug.
    Okumu A, DiMaso M, Löbenberg R.
    Pharm Res; 2008 Dec; 25(12):2778-85. PubMed ID: 18560996
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  • 4. Biorelevant dissolution media as a predictive tool for glyburide a class II drug.
    Wei H, Löbenberg R.
    Eur J Pharm Sci; 2006 Sep; 29(1):45-52. PubMed ID: 16815694
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  • 5. In vitro dissolution methodology, mini-Gastrointestinal Simulator (mGIS), predicts better in vivo dissolution of a weak base drug, dasatinib.
    Tsume Y, Takeuchi S, Matsui K, Amidon GE, Amidon GL.
    Eur J Pharm Sci; 2015 Aug 30; 76():203-12. PubMed ID: 25978875
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  • 6. Pharmacokinetic simulation of biowaiver criteria: the effects of gastric emptying, dissolution, absorption and elimination rates.
    Kortejärvi H, Urtti A, Yliperttula M.
    Eur J Pharm Sci; 2007 Feb 30; 30(2):155-66. PubMed ID: 17187967
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  • 7. Physicochemical investigation of the solid dispersion systems of etoricoxib with poloxamer 188.
    Karekar P, Vyas V, Shah M, Sancheti P, Pore Y.
    Pharm Dev Technol; 2009 Feb 30; 14(4):373-9. PubMed ID: 19552551
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  • 8. Analysis of the enhanced oral bioavailability of fenofibrate lipid formulations in fasted humans using an in vitro-in silico-in vivo approach.
    Fei Y, Kostewicz ES, Sheu MT, Dressman JB.
    Eur J Pharm Biopharm; 2013 Nov 30; 85(3 Pt B):1274-84. PubMed ID: 23500116
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  • 9. In silico predictions of gastrointestinal drug absorption in pharmaceutical product development: application of the mechanistic absorption model GI-Sim.
    Sjögren E, Westergren J, Grant I, Hanisch G, Lindfors L, Lennernäs H, Abrahamsson B, Tannergren C.
    Eur J Pharm Sci; 2013 Jul 16; 49(4):679-98. PubMed ID: 23727464
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  • 11. Understanding the in vivo performance of enteric coated tablets using an in vitro-in silico-in vivo approach: case example diclofenac.
    Kambayashi A, Blume H, Dressman J.
    Eur J Pharm Biopharm; 2013 Nov 16; 85(3 Pt B):1337-47. PubMed ID: 24056057
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  • 12. The biowaiver extension for BCS class III drugs: the effect of dissolution rate on the bioequivalence of BCS class III immediate-release drugs predicted by computer simulation.
    Tsume Y, Amidon GL.
    Mol Pharm; 2010 Aug 02; 7(4):1235-43. PubMed ID: 20557130
    [Abstract] [Full Text] [Related]

  • 13. Toward Biopredictive Dissolution for Enteric Coated Dosage Forms.
    Al-Gousous J, Amidon GL, Langguth P.
    Mol Pharm; 2016 Jun 06; 13(6):1927-36. PubMed ID: 27139040
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