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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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Koner, Jasdip S., Rajabi-Siahboomi, Ali R., Missaghi, Shahrzad, Kirby, Daniel, Perrie, Yvonne, Ahmed, Jiteen, Mohammed, Afzal R.
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6713731/
https://ncbi.nlm.nih.gov/pubmed/31462654
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-48859-x
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