Drug Development and Industrial Pharmacy, 0363-9045

Journal

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  1. 2010
  2. Drug release from lipid liquid crystalline phases: relation with phase behavior

    Costa, F., Emma Sparr, Simoes Sousa, J. J. & Pais, A. C., 2010, In : Drug Development and Industrial Pharmacy. 36, 4, p. 470-481

    Research output: Contribution to journalArticle

  3. 2009
  4. Oral-based controlled release formulations using poly(acrylic acid) microgels.

    M Wahlgren, Christensen, K. L., Jørgensen, E. V., Svensson, A. & S Ulvenlund, 2009, In : Drug Development and Industrial Pharmacy. 35, p. 922-929 8 p.

    Research output: Contribution to journalArticle

  5. 1987
  6. Optimizing the friability of a tablet formulation

    Lindberg, N-O. & Björn Holmquist, 1987, In : Drug Development and Industrial Pharmacy. 13, 6, p. 1063-1067

    Research output: Contribution to journalArticle

  7. 1985
  8. Optimization of disintegration time and crushing strength of a tablet formulation

    Lindberg, N-O., Jönsson, C. & Björn Holmquist, 1985, In : Drug Development and Industrial Pharmacy. 11, 4, p. 931-944

    Research output: Contribution to journalArticle

  9. The granulation of a tablet formulation in a high-speed mixer, Diosna P 25

    Lindberg, N-O., Jönsson, C. & Björn Holmquist, 1985, In : Drug Development and Industrial Pharmacy. 11, 4, p. 917-930

    Research output: Contribution to journalArticle