Reliable HPLC/UV Quantification of Nitrosamine Impurities in Valsartan and Ranitidine Drug Substances

Aplikace | 2019 | WatersInstrumentace
LC/MS, LC/SQ
Zaměření
Farmaceutická analýza
Výrobce
Waters
PDF verze ke stažení a čtení
 

Podobná PDF

Highly Sensitive and Robust UPLC-MS/MS Quantification of Nitrosamine Impurities in Sartan and Ranitidine Drug Substances
Use of a Proprietary Polar Column Chemistry for the Separation of Nitrosamines in Sartan and Ranitidine Drug Substances
Determination of six nitrosamine impurities in angiotensin II receptor blocker drugs by LC-MS/MS
Highly sensitive method for the determination of 12 nitrosamine impurities in multiple ARBs, the class of sartan drug formulations