| Literature DB >> 31078064 |
Oliver Scherf-Clavel1, Martina Kinzig2, Axel Besa3, André Schreiber3, Clemens Bidmon4, Mona Abdel-Tawab5, Jonas Wohlfart1, Fritz Sörgel6, Ulrike Holzgrabe1.
Abstract
The recent incidences of contaminated valsartan drug products gave rise to review the suitability of current impurity profiling workflows implemented at authorities and pharmaceutical companies. The major drawback of targeted impurity profiling, where a considerable amount of prior knowledge about possible contaminants is necessary, is the fact that unexpected impurities are overlooked easily. Here, a generic untargeted approach was applied on sartan containing drug products. The untargeted workflow allowed for the discrimination of different batches, different production sites, and differences after changes in the production process. The presented universal workflow makes use of LC-HRMS/MS and multivariate analysis for the interpretation of the data. Sartan samples contaminated with N-nitrosodimethylamine could be very well discriminated from N-nitrosodimethylamine-free samples using the procedure. Furthermore, untargeted approaches revealed two new impurities in various sartans drug products: valeramide and N,N-dimethylvaleramide.Entities:
Keywords: Contamination; LC–MS/HRMS; NDEA; NDMA; Nitrosamines; Valeramide; Valsartan
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Year: 2019 PMID: 31078064 DOI: 10.1016/j.jpba.2019.04.035
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935