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Development and application of a validated HPLC method for the analysis of dissolution samples of levothyroxine sodium drug products
A rapid, selective, and sensitive gradient HPLC method was developed for the analysis of dissolution samples of levothyroxine sodium tablets. Current USP methodology for levothyroxine (l-T(4)) was not adequate to resolve co-elutants from a variety of levothyroxine drug product formulations. The USP...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3090652/ https://ncbi.nlm.nih.gov/pubmed/20947276 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpba.2010.08.025 |
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