spectrofluorometric analysis of new-generation antidepressant drugs in pharmaceutical formulations, human urine, and plasma samplesspectrofluorometric分析新一代抗抑郁药物在制药配方,人类尿液和血浆样本.pdfVIP
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spectrofluorometric analysis of new-generation antidepressant drugs in pharmaceutical formulations, human urine, and plasma samplesspectrofluorometric分析新一代抗抑郁药物在制药配方,人类尿液和血浆样本
Hindawi Publishing Corporation
Spectroscopy: An International Journal
Volume 27 (2012), Issue 2, Pages 59–71
doi:10.1155/2012/567207
Spectrofluorometric Analysis of
New-Generation Antidepressant Drugs in
Pharmaceutical Formulations, Human Urine,
and Plasma Samples
Ruchita S. Das and Y. K. Agrawal
Institute of Research Development, Gujarat Forensic Sciences University, Sector 18-A,
Gandhinagar 382007, India
Correspondence should be addressed to Ruchita S. Das, das ruchita@
Copyright © 2012 R. S. Das and Y. K. Agrawal. This is an open access article distributed under the Creative Commons
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work
is properly cited.
Abstract. Spectrofluorometric analysis for the quantification of new-generation antidepressant drugs belong to the class
of selective serotonin reuptake inhibitors and selective norepinephrine reuptake inhibitors is described. Five different
drugs, sertraline, paroxetine, citalopram, venlafaxine, and fluoxetine, were analysed for spectrofluorometric detection in
pharmaceutical formulations and urine and plasma samples. The calibration curves were found linear between fluorescence
intensity and drugs concentration in the range of 5–500 ng/μL with coefficients of determination above 0.9985 for all the
analytes. The method recoveries were higher than 85% in all the three matrices. The intra- and interday variation coefficients
were observed less than 8% and 13%, respectively. The limits of detection (LOD) and limit of quantification (LOQ) were found
in the range of 0.016–0.084 ng/μL and 0.090–0.285 ng/μL, respectively. Additionally, the results were compared statistically
for each analyte in all the three matrices and were found equivalent, which signifies the absence of matrix effect. Thus, the
method will be applied successfully to the determination of the cited drug
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