Development of a stability-indicating UPLC method for determining olanzapine and its associated degradation products present in active pharmaceutical ingredients and pharmaceutical dosage forms. [electronic resource]
- Journal of pharmaceutical and biomedical analysis Mar 2011
- 667-73 p. digital
Publication Type: Journal Article; Validation Study
1873-264X
10.1016/j.jpba.2010.10.013 doi
Antipsychotic Agents--analysis Benzodiazepines--analysis Chromatography, High Pressure Liquid Drug Contamination--prevention & control Drug Stability Hot Temperature--adverse effects Hydrogen-Ion Concentration Limit of Detection Olanzapine Oxidation-Reduction Quality Control Reproducibility of Results Spectrometry, Mass, Electrospray Ionization Tandem Mass Spectrometry Technology, Pharmaceutical Time Factors Ultraviolet Rays--adverse effects