Cargando…
LC–UV and LC–MS evaluation of stress degradation behavior of desvenlafaxine
The objective of current study was to develop a validated specific stability indicating reversed-phase liquid chromatographic method for the quantitative determination of desvenlafaxine in bulk sample and pharmaceutical dosage form in the presence of degradation products. Forced degradation studies...
Autores principales: | Pawar, Shubhangi M., Khatal, Laxman D., Gabhe, Satish Y., Dhaneshwar, Sunil R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760900/ https://www.ncbi.nlm.nih.gov/pubmed/29403752 http://dx.doi.org/10.1016/j.jpha.2012.02.009 |
Ejemplares similares
-
Establishment of inherent stability of pramipexole and development of validated stability indicating LC–UV and LC–MS method
por: Pawar, Shubhangi M., et al.
Publicado: (2013) -
LC-MS/MS and LC-UV Determination of Moniliformin by Adding Lanthanide Ions to the Mobile Phase
por: Bertuzzi, Terenzio, et al.
Publicado: (2019) -
LC, MS(n) and LC–MS/MS studies for the characterization of degradation products of amlodipine
por: Tiwari, Ravi N., et al.
Publicado: (2015) -
LC and LC–MS/MS studies for the identification and characterization of degradation products of acebutolol
por: Rakibe, Uday, et al.
Publicado: (2018) -
Kinetics and Characterization of Degradation Products of Dihydralazine and Hydrochlorothiazide in Binary Mixture by HPLC-UV, LC-DAD and LC–MS Methods
por: Gumieniczek, Anna, et al.
Publicado: (2018)