Cargando…
LC–UV/MS quality analytics of paediatric artemether formulations
A highly selective and stability-indicating HPLC-method, combined with appropriate sample preparation steps, is developed for β-artemether assay and profiling of related impurities, including possible degradants, in a complex powder for oral suspension. Following HPLC conditions allowed the required...
Autores principales: | Vandercruyssen, Kirsten, D’Hondt, Matthias, Vergote, Valentijn, Jansen, Herwig, Burvenich, Christian, De Spiegeleer, Bart |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5761056/ https://www.ncbi.nlm.nih.gov/pubmed/29403867 http://dx.doi.org/10.1016/j.jpha.2013.03.006 |
Ejemplares similares
-
A rapid stability-indicating, fused-core HPLC method for simultaneous determination of β-artemether and lumefantrine in anti-malarial fixed dose combination products
por: Suleman, Sultan, et al.
Publicado: (2013) -
Derringer desirability and kinetic plot LC-column comparison approach for MS-compatible lipopeptide analysis
por: D’Hondt, Matthias, et al.
Publicado: (2014) -
Stability-indicating HPLC-DAD/UV-ESI/MS impurity profiling of the anti-malarial drug lumefantrine
por: Verbeken, Mathieu, et al.
Publicado: (2011) -
Gas chromatographic method for the determination of lumefantrine in antimalarial finished pharmaceutical products
por: Suleman, Sultan, et al.
Publicado: (2015) -
Quality of fixed dose artemether/lumefantrine products in Jimma Zone, Ethiopia
por: Belew, Sileshi, et al.
Publicado: (2019)