NIR hyperspectral imaging to evaluate degradation in captopril commercial tablets

Author:

França Leandro de Moura,Pimentel Maria Fernanda,Simões Simone da Silva,Grangeiro Severino,Prats-Montalbán José M.,Ferrer Alberto

Publisher

Elsevier BV

Subject

Pharmaceutical Science,General Medicine,Biotechnology

Reference42 articles.

1. Forced degradation and impurity profiling: recent trends in analytical perspectives;Jain;J. Pharm. Biomed. Anal.,2013

2. LC-MS/MS structural characterization of stress degradation products including the development of a stability indicating assay of Darunavir: an anti-HIV drug;Rao;J. Pharm. Biomed. Anal.,2014

3. ICH harmonised tripartite guideline: Q3B (R2) impurities in New Drug Substances, in: International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, 2006.

4. ICH harmonised tripartite guideline: Q1A (R2) Stability Testing of New Drug Substances and Products, in: International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use, 2003.

5. Tools and workflow for structure elucidation of drug degradation products;Foti;TrAC, Trends Anal. Chem.,2013

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