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Journal Abstract Search

150 related items for PubMed ID: 23891743

  • 21. Multimodal approach to characterization of hydrophilic matrices manufactured by wet and dry granulation or direct compression methods.
    Kulinowski P, Woyna-Orlewicz K, Obrał J, Rappen GM, Haznar-Garbacz D, Węglarz WP, Jachowicz R, Wyszogrodzka G, Klaja J, Dorożyński PP.
    Int J Pharm; 2016 Feb 29; 499(1-2):263-270. PubMed ID: 26752087
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. 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
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  • 24. The manufacture and characterisation of hot-melt extruded enteric tablets.
    Andrews GP, Jones DS, Diak OA, McCoy CP, Watts AB, McGinity JW.
    Eur J Pharm Biopharm; 2008 May 25; 69(1):264-73. PubMed ID: 18164604
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  • 25. Development of prednisone:polyethylene glycol 6000 fast-release tablets from solid dispersions: solid-state characterization, dissolution behavior, and formulation parameters.
    Leonardi D, Barrera MG, Lamas MC, Salomón CJ.
    AAPS PharmSciTech; 2007 Dec 14; 8(4):E108. PubMed ID: 18181529
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  • 26. Evaluation of the Microcentrifuge Dissolution Method as a Tool for Spray-Dried Dispersion.
    Wu B, Li J, Wang Y.
    AAPS J; 2016 Mar 14; 18(2):346-53. PubMed ID: 26831250
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  • 27. Formulation development and process scale up of a high shear wet granulation formulation containing a poorly wettable drug.
    He X, Lunday KA, Li LC, Sacchetti MJ.
    J Pharm Sci; 2008 Dec 14; 97(12):5274-89. PubMed ID: 18449937
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  • 28. Mechanistic investigation of food effect on disintegration and dissolution of BCS class III compound solid formulations: the importance of viscosity.
    Radwan A, Amidon GL, Langguth P.
    Biopharm Drug Dispos; 2012 Oct 14; 33(7):403-16. PubMed ID: 22782559
    [Abstract] [Full Text] [Related]

  • 29. Impact of micromeritic properties of an active pharmaceutical ingredient on its compaction behavior.
    Bindra DS, Desikan S.
    Pharm Dev Technol; 2015 Mar 14; 20(2):129-38. PubMed ID: 24219704
    [Abstract] [Full Text] [Related]

  • 30. Raman and thermal analysis of indomethacin/PVP solid dispersion enteric microparticles.
    Fini A, Cavallari C, Ospitali F.
    Eur J Pharm Biopharm; 2008 Sep 14; 70(1):409-20. PubMed ID: 18621516
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  • 31. Design of porous microparticles with single-micron size by novel spray freeze-drying technique using four-fluid nozzle.
    Niwa T, Shimabara H, Kondo M, Danjo K.
    Int J Pharm; 2009 Dec 01; 382(1-2):88-97. PubMed ID: 19686828
    [Abstract] [Full Text] [Related]

  • 32. An investigation into the effect of formulation variables and process parameters on characteristics of granules obtained by in situ fluidized hot melt granulation.
    Mašić I, Ilić I, Dreu R, Ibrić S, Parojčić J, Durić Z.
    Int J Pharm; 2012 Feb 28; 423(2):202-12. PubMed ID: 22197773
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  • 33. To evaluate the effect of addition of an anionic surfactant on solid dispersion using model drug indomethacin.
    Dave RH, Patel AD, Donahue E, Patel HH.
    Drug Dev Ind Pharm; 2012 Aug 28; 38(8):930-9. PubMed ID: 22085470
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  • 34. Development of an oral rutin nanocrystal formulation.
    Mauludin R, Müller RH, Keck CM.
    Int J Pharm; 2009 Mar 31; 370(1-2):202-9. PubMed ID: 19114097
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  • 35. In-vitro and in-vivo evaluation of enteric-coated starch-based pellets prepared via extrusion/spheronisation.
    Dukić-Ott A, De Beer T, Remon JP, Baeyens W, Foreman P, Vervaet C.
    Eur J Pharm Biopharm; 2008 Sep 31; 70(1):302-12. PubMed ID: 18579353
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  • 36. Preparation of glass solutions of three poorly water soluble drugs by spray drying, melt extrusion and ball milling.
    Patterson JE, James MB, Forster AH, Lancaster RW, Butler JM, Rades T.
    Int J Pharm; 2007 May 04; 336(1):22-34. PubMed ID: 17174493
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  • 37. Dry coating of micronized API powders for improved dissolution of directly compacted tablets with high drug loading.
    Han X, Ghoroi C, Davé R.
    Int J Pharm; 2013 Feb 14; 442(1-2):74-85. PubMed ID: 22921376
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  • 38. Maintenance of supersaturation I: indomethacin crystal growth kinetic modeling using an online second-derivative ultraviolet spectroscopic method.
    Patel DD, Joguparthi V, Wang Z, Anderson BD.
    J Pharm Sci; 2011 Jul 14; 100(7):2623-41. PubMed ID: 21259238
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  • 39. 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 14; 65(1):57-67. PubMed ID: 16987642
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  • 40. Improving the de-agglomeration and dissolution of a poorly water soluble drug by decreasing the agglomerate strength of the cohesive powder.
    Allahham A, Stewart PJ, Das SC.
    Int J Pharm; 2013 Nov 30; 457(1):101-9. PubMed ID: 24080334
    [Abstract] [Full Text] [Related]

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