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MRB7G43
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A liquid chromatography method was developed and validated for the determination of fluoxetine in human plasma using paroxetine as internal standard. The drugs were extracted from plasma by liquid-liquid extraction and separated isocratically on a C 18 analytical column, with water:acetonitrile as mobile phase, run at a flow rate of 0.20 mL/min. The method was linear in the range of 0.2-50 ng/mL and demonstrated acceptable results for the precision, accuracy and stability studies. The method was successfully applied for the bioequivalence study of two tablet formulations of fluoxetine 20 mg after single oral dose administration to healthy human volunteers.
Dr.Luciana Duarte. 1970. "FLUOXETINE BIOEQUIVALENCE STUDY: QUANTIFICATION OF FLUOXETINE BY LIQUID CHROMATOGRAPHY COUPLED TO MASS SPECTROMETRY". Global Journal of Medical Research GJMR Volume 10 (GJMR Volume 10 Issue 2).
Crossref Journal DOI 10.17406/gjmr
Print ISSN 0975-5888
e-ISSN 2249-4618
v1.2
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Total Score: 149
Country: Unknown
Subject: Global Journal of Medical Research
Authors: Dr.Luciana Fernandes Duarte, Lara Cristina Silva, Moiss L. P. Vanunci, Tatiane A. M. Stein e Marina M. Nakamura (PhD/Dr. count: 1)
View Count (all-time): 223
Total Views (Real + Logic): 4959
Total Downloads (simulated): 132
Publish Date: 2010 05, Sat
Monthly Totals (Real + Logic):
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