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Journal Abstract Search

247 related items for PubMed ID: 17879295

  • 21. Influence of loading volume of mefenamic acid on granules and tablet characteristics using a compaction simulator.
    Kimura G, Betz G, Leuenberger H.
    Pharm Dev Technol; 2008; 13(1):57-64. PubMed ID: 18300100
    [Abstract] [Full Text] [Related]

  • 22. Comparison of Disintegrant-addition Methods on the Compounding of Orodispersible Tablets.
    Mahesparan VA, Bin Abd Razak FS, Ming LC, Uddin AH, Sarker MZI, Bin LK.
    Int J Pharm Compd; 2020; 24(2):148-155. PubMed ID: 32196477
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  • 23. Development of a rapidly dispersing tablet of a poorly wettable compound: formulation DOE and mechanistic study of effect of formulation excipients on wetting of celecoxib.
    He X, Barone MR, Marsac PJ, Sperry DC.
    Int J Pharm; 2008 Apr 02; 353(1-2):176-86. PubMed ID: 18207339
    [Abstract] [Full Text] [Related]

  • 24. The influence of API concentration on the roller compaction process: modeling and prediction of the post compacted ribbon, granule and tablet properties using multivariate data analysis.
    Boersen N, Carvajal MT, Morris KR, Peck GE, Pinal R.
    Drug Dev Ind Pharm; 2015 Apr 02; 41(9):1470-8. PubMed ID: 25212638
    [Abstract] [Full Text] [Related]

  • 25. Modifying drug release and tablet properties of starch acetate tablets by dry powder agglomeration.
    Mäki R, Suihko E, Rost S, Heiskanen M, Murtomaa M, Lehto VP, Ketolainen J.
    J Pharm Sci; 2007 Feb 02; 96(2):438-47. PubMed ID: 17075868
    [Abstract] [Full Text] [Related]

  • 26. Predicting the tensile strength of compacted multi-component mixtures of pharmaceutical powders.
    Wu CY, Best SM, Bentham AC, Hancock BC, Bonfield W.
    Pharm Res; 2006 Aug 02; 23(8):1898-905. PubMed ID: 16850273
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  • 27. Assessment of disintegrant efficacy with fractal dimensions from real-time MRI.
    Quodbach J, Moussavi A, Tammer R, Frahm J, Kleinebudde P.
    Int J Pharm; 2014 Nov 20; 475(1-2):605-12. PubMed ID: 25234864
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  • 28. Taro starch (Colocasia esculenta) and citric acid modified taro starch as tablet disintegrating agents.
    Pachuau L, Dutta RS, Devi TB, Deka D, Hauzel L.
    Int J Biol Macromol; 2018 Oct 15; 118(Pt A):397-405. PubMed ID: 29935240
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  • 34. Development of novel sustained-release system, disintegration-controlled matrix tablet (DCMT) with solid dispersion granules of nilvadipine.
    Tanaka N, Imai K, Okimoto K, Ueda S, Tokunaga Y, Ohike A, Ibuki R, Higaki K, Kimura T.
    J Control Release; 2005 Nov 28; 108(2-3):386-95. PubMed ID: 16253377
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  • 39. Enhancing tablet disintegration characteristics of a highly water-soluble high-drug-loading formulation by granulation process.
    Pandey P, Levins C, Pafiakis S, Zacour B, Bindra DS, Trinh J, Buckley D, Gour S, Sharif S, Stamato H.
    Pharm Dev Technol; 2018 Jul 28; 23(6):587-595. PubMed ID: 27879156
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