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Volumn 23, Issue 3, 2010, Pages 212-218
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A validated thin-layer chromatographic method for analysis of bupropion hydrochloride in a pharmaceutical dosage form
a
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Author keywords
Bupropion hydrochloride; Method validation; Stability; Tablet analysis; Thin layer chromatography (TLC)
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Indexed keywords
ALKALINE HYDROLYSIS;
BUPROPION;
CHROMATOGRAPHIC METHODS;
CONTROL STANDARDS;
DEGRADATION PRODUCTS;
DENSITOMETRIC ANALYSIS;
DRY AND WET;
GLACIAL ACETIC ACID;
HPLC ANALYSIS;
INTER-DAY REPEATABILITY;
LIMITS OF DETECTION AND QUANTITATION;
LINEAR RELATIONSHIPS;
METHOD VALIDATION;
METHOD VALIDATIONS;
MOBILE PHASE;
PEAK AREA;
PHARMACEUTICAL DOSAGE FORMS;
PHARMACEUTICAL TABLETS;
SELECTIVE ANALYSIS;
STATISTICAL COMPARISONS;
SYNTHETIC MIXTURES;
THIN LAYERS;
ACIDS;
CHROMATOGRAPHIC ANALYSIS;
DRUG PRODUCTS;
ETHANOL;
PHOTODEGRADATION;
REGRESSION ANALYSIS;
SILICA;
SILICA GEL;
THIN LAYER CHROMATOGRAPHY;
QUALITY CONTROL;
ACETIC ACID;
ALCOHOL;
AMFEBUTAMONE;
CHLOROFORM;
SILICA GEL;
ACCURACY;
CONFERENCE PAPER;
DENSITOMETRY;
DRUG STRUCTURE;
HYDROLYSIS;
LINEAR REGRESSION ANALYSIS;
OXIDATION;
PHOTODEGRADATION;
QUALITY CONTROL;
STATISTICAL ANALYSIS;
TABLET;
THIN LAYER CHROMATOGRAPHY;
VALIDATION PROCESS;
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EID: 77953848575
PISSN: 09334173
EISSN: None
Source Type: Journal
DOI: 10.1556/JPC.23.2010.3.9 Document Type: Conference Paper |
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Times cited : (12)
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References (22)
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