000 01713 a2200433 4500
005 20250516012642.0
264 0 _c20110418
008 201104s 0 0 eng d
022 _a1873-264X
024 7 _a10.1016/j.jpba.2010.10.013
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aKrishnaiah, Ch
245 0 0 _aDevelopment of a stability-indicating UPLC method for determining olanzapine and its associated degradation products present in active pharmaceutical ingredients and pharmaceutical dosage forms.
_h[electronic resource]
260 _bJournal of pharmaceutical and biomedical analysis
_cMar 2011
300 _a667-73 p.
_bdigital
500 _aPublication Type: Journal Article; Validation Study
650 0 4 _aAntipsychotic Agents
_xanalysis
650 0 4 _aBenzodiazepines
_xanalysis
650 0 4 _aChromatography, High Pressure Liquid
650 0 4 _aDrug Contamination
_xprevention & control
650 0 4 _aDrug Stability
650 0 4 _aHot Temperature
_xadverse effects
650 0 4 _aHydrogen-Ion Concentration
650 0 4 _aLimit of Detection
650 0 4 _aOlanzapine
650 0 4 _aOxidation-Reduction
650 0 4 _aQuality Control
650 0 4 _aReproducibility of Results
650 0 4 _aSpectrometry, Mass, Electrospray Ionization
650 0 4 _aTandem Mass Spectrometry
650 0 4 _aTechnology, Pharmaceutical
650 0 4 _aTime Factors
650 0 4 _aUltraviolet Rays
_xadverse effects
700 1 _aVishnu Murthy, M
700 1 _aKumar, Ramesh
700 1 _aMukkanti, K
773 0 _tJournal of pharmaceutical and biomedical analysis
_gvol. 54
_gno. 4
_gp. 667-73
856 4 0 _uhttps://doi.org/10.1016/j.jpba.2010.10.013
_zAvailable from publisher's website
999 _c20373112
_d20373112