Tablet Disintegration Testing

Tablet Disintegration Testing is a standardized pharmaceutical evaluation method that determines the time and conditions under which a tablet breaks down into smaller aggregates or granules in a specified medium, distinguishing it from other dosage form assessments by its focus on the physical breakdown process essential for drug dissolution and absorption.

337

Publications

11.5K

Citations

1.2K

Authors

366

Institutions

Publications per year

2017–2026

76

Variants

Disintegration Test

Publications

337

1–5 of 337

Authors

1.2K

  1. RL
    Raimar Löbenberg

    University of Alberta, Canada

    7 publications · 143 citations

    7

    h-index

  2. PK
    Peter Kleinebudde

    Heinrich Heine University Düsseldorf, Germany

    5 publications · 209 citations

    5

    h-index

  3. PC
    Paolo Colombo

    University of Parma, Italy

    5 publications · 182 citations

    5

    h-index

  4. UC
    U. Conte

    University of Pavia, Italy

    5 publications · 160 citations

    5

    h-index

  5. DM
    Daniel Markl

    University of Strathclyde, United Kingdom

    5 publications · 278 citations

    5

    h-index

1–5 of 1.2K

Venues

  1. International Journal of Pharmaceutics

    51 publications · 2.3K citations

    30

    h-index

  2. Journal of Pharmaceutical Sciences

    38 publications · 1.2K citations

    20

    h-index

  3. AAPS PharmSciTech

    15 publications · 596 citations

    14

    h-index

  4. PubMed

    Repository · 17 publications · 337 citations

    12

    h-index

  5. Drug Development and Industrial Pharmacy

    18 publications · 407 citations

    12

    h-index

1–5