Conceptualisation, Development, Fabrication and In Vivo Validation of a Novel Disintegration Tester for Orally Disintegrating Tablets

Disintegration time is the key critical quality attribute for a tablet classed as an Orally Disintegrating Tablet (ODT). The currently accepted in vitro testing regimen for ODTs is the standard United States Pharmacopeia (USP) test for disintegration of immediate release tablets, which requires a la...

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Detalles Bibliográficos
Autores principales: Koner, Jasdip S., Rajabi-Siahboomi, Ali R., Missaghi, Shahrzad, Kirby, Daniel, Perrie, Yvonne, Ahmed, Jiteen, Mohammed, Afzal R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713731/
https://www.ncbi.nlm.nih.gov/pubmed/31462654
http://dx.doi.org/10.1038/s41598-019-48859-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713731/
https://www.ncbi.nlm.nih.gov/pubmed/31462654
http://dx.doi.org/10.1038/s41598-019-48859-x

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