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Miniaturized hollow fibre assisted liquid‐phase microextraction and gas chromatography for determination of trace concentration of sufentanil and alfentanil in biological samples
Author(s) -
Fakhari Ali Reza,
Tabani Hadi,
Nojavan Saeed
Publication year - 2013
Publication title -
drug testing and analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.065
H-Index - 54
eISSN - 1942-7611
pISSN - 1942-7603
DOI - 10.1002/dta.1387
Subject(s) - alfentanil , sufentanil , chromatography , chemistry , extraction (chemistry) , detection limit , solvent , injection port , gas chromatography , flame ionization detector , materials science , anesthesia , fentanyl , organic chemistry , composite material , medicine
A simple and highly sensitive method that involves miniaturized hollow fibre assisted liquid‐phase microextraction with gas chromatography‐flame ionization detector was developed for the determination of trace concentration of sufentanil and alfentanil in biological samples. These drugs were extracted from 5 ml of aqueous solution with pH 10.0 into an organic extracting solvent (1‐octanol) impregnated in the pores and lumen of a hollow fibre. After extraction for a prescribed time, 2.0 µl of the extraction solvent was injected directly in to the GC injection port. Under the optimized conditions, (1‐octanol as extracting solvent, stirring rate of 700 rpm, 15% ( w/v ) salt addition, pH 10.0 and 25 min sampling time at 50 °C) large enrichment factors of 535 and 420 were achieved for sufentanil and alfentanil, respectively. Dynamic linear ranges were in the range of 0.05 to 500 ng/ml for sufentanil and 0.1 to 500 ng/ml for alfentanil. Limits of detection 0.01 and 0.02 ng/ml were obtained for sufentanil and alfentanil, respectively. The percent relative intra‐day and inter‐day standard deviations were found to be less than 8.4% (n = 5). Finally, this method was successfully applied for the separation, preconcentration and determination of trace concentration of sufentanil and alfentanil in plasma and urine samples. Copyright © 2012 John Wiley & Sons, Ltd.