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PUBMED FOR HANDHELDS

Journal Abstract Search


221 related items for PubMed ID: 19815062

  • 21. Enhancement of oral bioavailability of an HIV-attachment inhibitor by nanosizing and amorphous formulation approaches.
    Fakes MG, Vakkalagadda BJ, Qian F, Desikan S, Gandhi RB, Lai C, Hsieh A, Franchini MK, Toale H, Brown J.
    Int J Pharm; 2009 Mar 31; 370(1-2):167-74. PubMed ID: 19100319
    [Abstract] [Full Text] [Related]

  • 22. Is bicarbonate buffer suitable as a dissolution medium?
    Boni JE, Brickl RS, Dressman J.
    J Pharm Pharmacol; 2007 Oct 31; 59(10):1375-82. PubMed ID: 17910812
    [Abstract] [Full Text] [Related]

  • 23. An innovative floating gastro retentive dosage system: formulation and in vitro evaluation.
    Sauzet C, Claeys-Bruno M, Nicolas M, Kister J, Piccerelle P, Prinderre P.
    Int J Pharm; 2009 Aug 13; 378(1-2):23-9. PubMed ID: 19465095
    [Abstract] [Full Text] [Related]

  • 24. Optimizing solubility: kinetic versus thermodynamic solubility temptations and risks.
    Saal C, Petereit AC.
    Eur J Pharm Sci; 2012 Oct 09; 47(3):589-95. PubMed ID: 22885099
    [Abstract] [Full Text] [Related]

  • 25. Estimating drug solubility in the gastrointestinal tract.
    Dressman JB, Vertzoni M, Goumas K, Reppas C.
    Adv Drug Deliv Rev; 2007 Jul 30; 59(7):591-602. PubMed ID: 17599644
    [Abstract] [Full Text] [Related]

  • 26. Estimating the maximal solubility advantage of drug salts.
    Skrdla PJ.
    Int J Pharm; 2021 Feb 15; 595():120228. PubMed ID: 33484924
    [Abstract] [Full Text] [Related]

  • 27. Simultaneous measurement of liquid-phase and solid-phase transformation kinetics in rotating disc and channel flow cell dissolution devices.
    Lehto P, Aaltonen J, Niemelä P, Rantanen J, Hirvonen J, Tanninen VP, Peltonen L.
    Int J Pharm; 2008 Nov 03; 363(1-2):66-72. PubMed ID: 18675891
    [Abstract] [Full Text] [Related]

  • 28. Measurement and Accurate Interpretation of the Solubility of Pharmaceutical Salts.
    He Y, Ho C, Yang D, Chen J, Orton E.
    J Pharm Sci; 2017 May 03; 106(5):1190-1196. PubMed ID: 28153596
    [Abstract] [Full Text] [Related]

  • 29. The apparent solubilizing capacity of simulated intestinal fluids for poorly water-soluble drugs.
    Schwebel HJ, van Hoogevest P, Leigh ML, Kuentz M.
    Pharm Dev Technol; 2011 Jun 03; 16(3):278-86. PubMed ID: 20214530
    [Abstract] [Full Text] [Related]

  • 30. 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 03; 30(2):155-66. PubMed ID: 17187967
    [Abstract] [Full Text] [Related]

  • 31. Plasma profiles of lycopene after single oral and intravenous administrations in dogs.
    Vertzoni M, Valsami G, Reppas C.
    J Pharm Pharmacol; 2006 Sep 03; 58(9):1211-7. PubMed ID: 16945179
    [Abstract] [Full Text] [Related]

  • 32. Simulation of fasting gastric conditions and its importance for the in vivo dissolution of lipophilic compounds.
    Vertzoni M, Dressman J, Butler J, Hempenstall J, Reppas C.
    Eur J Pharm Biopharm; 2005 Aug 03; 60(3):413-7. PubMed ID: 15893920
    [Abstract] [Full Text] [Related]

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  • 37. Dissolution and pharmacokinetics of baicalin-polyvinylpyrrolidone coprecipitate.
    Li B, He M, Li W, Luo Z, Guo Y, Li Y, Zang C, Wang B, Li F, Li S, Ji P.
    J Pharm Pharmacol; 2013 Nov 03; 65(11):1670-8. PubMed ID: 24111594
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  • 38. Method for screening of solid dispersion formulations of low-solubility compounds--miniaturization and automation of solvent casting and dissolution testing.
    Shanbhag A, Rabel S, Nauka E, Casadevall G, Shivanand P, Eichenbaum G, Mansky P.
    Int J Pharm; 2008 Mar 03; 351(1-2):209-18. PubMed ID: 18054181
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