Development of a new methodology for the determination of N-nitrosamines impurities in ranitidine pharmaceuticals using microextraction and gas chromatography-mass spectrometry
Author:
Funder
Consejería de Educación e Investigación
Ministerio de Ciencia e Innovación
Publisher
Elsevier BV
Subject
Analytical Chemistry
Reference23 articles.
1. Ingested nitrate and nitrite, and cyanobacterial peptide toxins,2010
2. NDMA impurity in valsartan and other pharmaceutical products: analytical methods for the determination of N-nitrosamines;Parr;J. Pharmaceut. Biomed. Anal.,2019
3. Sartan Medicines: Companies to Review Manufacturing Processes to Avoid Presence of Nitrosamine Impurities,2019
4. Characterization of pharmaceuticals and personal care products as N-nitrosodimethylamine precursors during disinfection processes using free chlorine and chlorine dioxide;Zhang;J. Hazard Mater.,2014
5. Characterization of N-nitrosodimethylamine formation from the ozonation of ranitidine;Lv;J. Environ. Sci.,2017
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