Management of validation of HPLC method for determination of acetylsalicylic acid impurities in a new pharmaceutical product

The work mainly focused on a validation of the method for determining the content of salicylic acid and individual unknown impurities in new pharmaceutical product—tablets containing: 75, 100 or 150 mg of acetylsalicylic acid and glycine in the amount of 40 mg for each dosage. The separation of the...

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Detalles Bibliográficos
Autores principales: Kowalska, Małgorzata, Woźniak, Magdalena, Kijek, Michał, Mitrosz, Paulina, Szakiel, Jerzy, Turek, Paweł
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738756/
https://www.ncbi.nlm.nih.gov/pubmed/34992227
http://dx.doi.org/10.1038/s41598-021-99269-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738756/
https://www.ncbi.nlm.nih.gov/pubmed/34992227
http://dx.doi.org/10.1038/s41598-021-99269-x

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