Development and Validation of a Precise, Single HPLC Method for the Determination of Tolperisone Impurities in API and Pharmaceutical Dosage Forms

A novel, sensitive, stability-indicating HPLC method has been developed for the quantitative estimation of Tolperisone-related impurities in both bulk drugs and pharmaceutical dosage forms. Effective chromatographic separation was achieved on a C18 stationary phase with a simple mobile phase combina...

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Detalles Bibliográficos
Autores principales: Raju, Thummala Veera Raghava, Seshadri, Raja Kumar, Arutla, Srinivas, Mohan, Tharlapu Satya Sankarsana Jagan, Rao, Ivaturi Mrutyunjaya, Nittala, Someswara Rao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617673/
https://www.ncbi.nlm.nih.gov/pubmed/23641333
http://dx.doi.org/10.3797/scipharm.1209-17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617673/
https://www.ncbi.nlm.nih.gov/pubmed/23641333
http://dx.doi.org/10.3797/scipharm.1209-17

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