Cargando…
Fully-automated system for dissolution rate of solid oral dosage forms according to the paddle method
This paper describes a fully-automated system (AUTO DISS(®)) for the determination of active ingredient release of solid oral dosage forms according to the paddle method of the US Pharmacopoeia (USP) and European Pharmacopoeia. Twenty batches can be tested continuously, with the six individuals (tab...
Autores principales: | Lamparter, Erich, Riedl, Dieter |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
1993
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2548022/ https://www.ncbi.nlm.nih.gov/pubmed/18924973 http://dx.doi.org/10.1155/S1463924693000239 |
Ejemplares similares
-
The Role of Functional Excipients in Solid Oral Dosage Forms to Overcome Poor Drug Dissolution and Bioavailability
por: van der Merwe, Jannes, et al.
Publicado: (2020) -
Control of Drug Dissolution Rate from Film Dosage Forms Containing Valsartan
por: Murata, Yoshifumi, et al.
Publicado: (2016) -
Dissolution Profile of Mefenamic Acid Solid Dosage Forms in Two Compendial and Biorelevant (FaSSIF) Media
por: Nurhikmah, Wilda, et al.
Publicado: (2016) -
Development of Flow-Through Cell Dissolution Method for In Situ Visualization of Dissolution Processes in Solid Dosage Forms Using X-ray μCT
por: Moazami Goudarzi, Niloofar, et al.
Publicado: (2022) -
Attitude of doctors towards physical characteristics of solid oral dosage forms
por: Hasamnis, A. A., et al.
Publicado: (2010)