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High performance liquid chromatographic determination of ultra traces of two tricyclic antidepressant drugs imipramine and trimipramine in urine samples after their dispersive liquid-liquid microextraction coupled with response surface optimization.
- Source :
-
Journal of pharmaceutical and biomedical analysis [J Pharm Biomed Anal] 2014 Nov; Vol. 100, pp. 271-278. Date of Electronic Publication: 2014 Aug 13. - Publication Year :
- 2014
-
Abstract
- Dispersive liquid-liquid microextraction (DLLME) coupled with high performance liquid chromatography by ultraviolet detection (HPLC-UV) as a fast and inexpensive technique was applied to the determination of imipramine and trimipramine in urine samples. Response surface methodology (RSM) was used for multivariate optimization of the effects of seven different parameters influencing the extraction efficiency of the proposed method. Under optimized experimental conditions, the enrichment factors and extraction recoveries were between 161.7-186.7 and 97-112%, respectively. The linear range and limit of detection for both analytes found to be 5-100ng mL(-1) and 0.6ng mL(-1), respectively. The relative standard deviations for 5ng mL(-1) of the drugs in urine samples were in the range of 5.1-6.1 (n=5). The developed method was successfully applied to real urine sample analyses.<br /> (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Subjects :
- Antidepressive Agents, Tricyclic pharmacokinetics
Calibration
Humans
Imipramine pharmacokinetics
Limit of Detection
Linear Models
Male
Multivariate Analysis
Reference Standards
Reproducibility of Results
Solvents chemistry
Spectrophotometry, Ultraviolet
Trimipramine pharmacokinetics
Antidepressive Agents, Tricyclic urine
Chromatography, High Pressure Liquid standards
Imipramine urine
Liquid Phase Microextraction standards
Models, Statistical
Trimipramine urine
Subjects
Details
- Language :
- English
- ISSN :
- 1873-264X
- Volume :
- 100
- Database :
- MEDLINE
- Journal :
- Journal of pharmaceutical and biomedical analysis
- Publication Type :
- Academic Journal
- Accession number :
- 25178259
- Full Text :
- https://doi.org/10.1016/j.jpba.2014.08.008