Dissolution test for citalopram in tablets and comparison of in vitro dissolution profiles

European Journal of Pharmaceutics and Biopharmaceutics

Volumn 67, Issue 2, 2007, Pages 524-530

  Menegola, Júlia ^a   Steppe, Martin ^a   Schapoval, Elfrides E S ^a  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO SUL   (Brazil)

Author keywords

Citalopram; Dissolution profile comparisons; Dissolution test; HPLC; Quality control

Indexed keywords

CITALOPRAM;

ARTICLE; DRUG QUALITY; DRUG SOLUBILITY; DRUG SPECIFICITY; DRUG STABILITY; DRUG STRUCTURE; IN VITRO STUDY; PHARMACEUTICAL ENGINEERING; QUANTITATIVE ANALYSIS; REVERSED PHASE LIQUID CHROMATOGRAPHY; TABLET FORMULATION; TABLET PROPERTY; VALIDITY;

CHROMATOGRAPHY; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CHROMATOGRAPHY, LIQUID; CITALOPRAM; HYDROCHLORIC ACID; HYDROGEN-ION CONCENTRATION; MODELS, CHEMICAL; QUALITY CONTROL; REPRODUCIBILITY OF RESULTS; SENSITIVITY AND SPECIFICITY; SPECTROPHOTOMETRY, ULTRAVIOLET; TABLETS; TIME FACTORS;

EID: 34547702280     PISSN: 09396411     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejpb.2007.02.009     Document Type: Article

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