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Journal Abstract Search

958 related items for PubMed ID: 17597252

  • 1. Crystal engineering of active pharmaceutical ingredients to improve solubility and dissolution rates.
    Blagden N, de Matas M, Gavan PT, York P.
    Adv Drug Deliv Rev; 2007 Jul 30; 59(7):617-30. PubMed ID: 17597252
    [Abstract] [Full Text] [Related]

  • 2. High-throughput crystallization: polymorphs, salts, co-crystals and solvates of pharmaceutical solids.
    Morissette SL, Almarsson O, Peterson ML, Remenar JF, Read MJ, Lemmo AV, Ellis S, Cima MJ, Gardner CR.
    Adv Drug Deliv Rev; 2004 Feb 23; 56(3):275-300. PubMed ID: 14962582
    [Abstract] [Full Text] [Related]

  • 3. The role of cocrystals in pharmaceutical science.
    Shan N, Zaworotko MJ.
    Drug Discov Today; 2008 May 23; 13(9-10):440-6. PubMed ID: 18468562
    [Abstract] [Full Text] [Related]

  • 4. Supercritical fluid particle design for poorly water-soluble drugs (review).
    Sun Y.
    Curr Pharm Des; 2014 May 23; 20(3):349-68. PubMed ID: 23651403
    [Abstract] [Full Text] [Related]

  • 5. Prodrug approaches for enhancing the bioavailability of drugs with low solubility.
    Müller CE.
    Chem Biodivers; 2009 Nov 23; 6(11):2071-83. PubMed ID: 19937841
    [Abstract] [Full Text] [Related]

  • 6. Supercritical carbon dioxide processing of active pharmaceutical ingredients for polymorphic control and for complex formation.
    Moribe K, Tozuka Y, Yamamoto K.
    Adv Drug Deliv Rev; 2008 Feb 14; 60(3):328-38. PubMed ID: 18006109
    [Abstract] [Full Text] [Related]

  • 7. Rationalizing the selection of oral lipid based drug delivery systems by an in vitro dynamic lipolysis model for improved oral bioavailability of poorly water soluble drugs.
    Dahan A, Hoffman A.
    J Control Release; 2008 Jul 02; 129(1):1-10. PubMed ID: 18499294
    [Abstract] [Full Text] [Related]

  • 8. Solid dispersions as strategy to improve oral bioavailability of poor water soluble drugs.
    Vasconcelos T, Sarmento B, Costa P.
    Drug Discov Today; 2007 Dec 02; 12(23-24):1068-75. PubMed ID: 18061887
    [Abstract] [Full Text] [Related]

  • 9. Novel ultra-rapid freezing particle engineering process for enhancement of dissolution rates of poorly water-soluble drugs.
    Overhoff KA, Engstrom JD, Chen B, Scherzer BD, Milner TE, Johnston KP, Williams RO.
    Eur J Pharm Biopharm; 2007 Jan 02; 65(1):57-67. PubMed ID: 16987642
    [Abstract] [Full Text] [Related]

  • 10. Enhancement of dissolution rate of poorly-soluble active ingredients by supercritical fluid processes. Part I: Micronization of neat particles.
    Perrut M, Jung J, Leboeuf F.
    Int J Pharm; 2005 Jan 06; 288(1):3-10. PubMed ID: 15607252
    [Abstract] [Full Text] [Related]

  • 11. Modification of physicochemical characteristics of active pharmaceutical ingredients and application of supersaturatable dosage forms for improving bioavailability of poorly absorbed drugs.
    Kawakami K.
    Adv Drug Deliv Rev; 2012 May 01; 64(6):480-95. PubMed ID: 22265844
    [Abstract] [Full Text] [Related]

  • 12. Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.
    Kawabata Y, Wada K, Nakatani M, Yamada S, Onoue S.
    Int J Pharm; 2011 Nov 25; 420(1):1-10. PubMed ID: 21884771
    [Abstract] [Full Text] [Related]

  • 13. Pharmaceutical cocrystals and poorly soluble drugs.
    Thakuria R, Delori A, Jones W, Lipert MP, Roy L, Rodríguez-Hornedo N.
    Int J Pharm; 2013 Aug 30; 453(1):101-25. PubMed ID: 23207015
    [Abstract] [Full Text] [Related]

  • 14. Solid-state interactions of calixarenes with biorelevant molecules.
    Danylyuk O, Suwinska K.
    Chem Commun (Camb); 2009 Oct 21; (39):5799-813. PubMed ID: 19787105
    [Abstract] [Full Text] [Related]

  • 15. Fast-dissolving microparticles fail to show improved oral bioavailability.
    Wong SM, Kellaway IW, Murdan S.
    J Pharm Pharmacol; 2006 Oct 21; 58(10):1319-26. PubMed ID: 17034654
    [Abstract] [Full Text] [Related]

  • 16. [Progress in the research of amorphous pharmaceuticals].
    Ying J, Lü Y, Du GH.
    Yao Xue Xue Bao; 2009 May 21; 44(5):443-8. PubMed ID: 19618716
    [Abstract] [Full Text] [Related]

  • 17. Solid dispersions, part I: recent evolutions and future opportunities in manufacturing methods for dissolution rate enhancement of poorly water-soluble drugs.
    Bikiaris DN.
    Expert Opin Drug Deliv; 2011 Nov 21; 8(11):1501-19. PubMed ID: 21919807
    [Abstract] [Full Text] [Related]

  • 18. Regulatory aspects of drug dissolution from a European perspective.
    Graffner C.
    Eur J Pharm Sci; 2006 Nov 21; 29(3-4):288-93. PubMed ID: 16950606
    [Abstract] [Full Text] [Related]

  • 19. Polymorph selection: the role of nucleation, crystal growth and molecular modeling.
    Erdemir D, Lee AY, Myerson AS.
    Curr Opin Drug Discov Devel; 2007 Nov 21; 10(6):746-55. PubMed ID: 17987526
    [Abstract] [Full Text] [Related]

  • 20. Strategies to improve oral drug bioavailability.
    Gomez-Orellana I.
    Expert Opin Drug Deliv; 2005 May 21; 2(3):419-33. PubMed ID: 16296764
    [Abstract] [Full Text] [Related]

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