Development and validation of a RP-HPLC method for stability-indicating assay of gemifloxacin mesylate including identification of related substances by LC-ESI-MS/MS, 1H and 13C NMR spectroscopy
ACCURACY;
ACIDITY;
ALKALINITY;
ARTICLE;
CARBON NUCLEAR MAGNETIC RESONANCE;
DRUG DETERMINATION;
DRUG IMPURITY;
DRUG STRUCTURE;
ELECTROSPRAY MASS SPECTROMETRY;
LIQUID CHROMATOGRAPHY;
PHOTOLYSIS;
PROTON NUCLEAR MAGNETIC RESONANCE;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
SEPARATION TECHNIQUE;
THERMAL ANALYSIS;
VALIDATION PROCESS;
CHEMISTRY;
DRUG CONTAMINATION;
HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY;
PROCEDURES;
REPRODUCIBILITY;
REVERSED PHASE LIQUID CHROMATOGRAPHY;
SENSITIVITY AND SPECIFICITY;
STATISTICAL MODEL;
TANDEM MASS SPECTROMETRY;
VALIDATION STUDY;
CHROMATOGRAPHY, HIGH PRESSURE LIQUID;
CHROMATOGRAPHY, REVERSE-PHASE;
DRUG CONTAMINATION;
FLUOROQUINOLONES;
LINEAR MODELS;
MAGNETIC RESONANCE SPECTROSCOPY;
NAPHTHYRIDINES;
REPRODUCIBILITY OF RESULTS;
SENSITIVITY AND SPECIFICITY;
TANDEM MASS SPECTROMETRY;
A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant
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6
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Chiral counter-current chromatography of gemifloxacin guided by capillary electrophoresis using (+)-(18-crown-6)-tetracarboxylic acid as a chiral selector
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Direct liquid chromatographic enantiomer separation of new fluoroquinolones including gemifloxacin
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Stability indicating RP-LC method for the determination of gemifloxacin mesylate
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An overview of the recent trends in development HPLC methods for determination of impurities in drugs
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Isolation and characterization of process related impurities and degradation products of bicalutamide and development of RP-HPLC method for impurity profile study
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