Disintegration Endpoints

Disintegration Endpoints is a methodological construct in pharmaceutical science that specifies the precise conditions or criteria under which a capsule formulation undergoes complete breakdown into its constituent particles in a defined medium, distinguishing it from related measures of dissolution or release kinetics by focusing exclusively on the physical disassembly of the dosage form.

32

Publications

1.1K

Citations

134

Authors

48

Institutions

Publications per year

2017–2026

8

Authors

134

  1. TU
    Takahiro Uchida

    Mukogawa Women's University, Japan

    3 publications · 42 citations

    3

    h-index

  2. RL
    Raimar Löbenberg

    University of Alberta, Canada

    2 publications · 28 citations

    2

    h-index

  3. MA
    May Almukainzi

    Princess Nourah bint Abdulrahman University, Saudi Arabia

    2 publications · 28 citations

    2

    h-index

  4. TH
    Tamami Haraguchi

    Mukogawa Women's University, Japan

    2 publications · 29 citations

    2

    h-index

  5. LW
    L.Y. Wang

    University of Minnesota, United States

    2 publications · 50 citations

    2

    h-index

1–5 of 134

Venues

  1. Journal of Pharmaceutical Sciences

    5 publications · 142 citations

    5

    h-index

  2. Powder Technology

    3 publications · 59 citations

    3

    h-index

  3. European Journal of Pharmaceutics and Biopharmaceutics

    EJPB · 2 publications · 127 citations

    2

    h-index

  4. Dissolution Technologies

    2 publications · 26 citations

    2

    h-index

  5. Journal of Drug Delivery Science and Technology

    JDDST · 2 publications · 32 citations

    2

    h-index

1–5