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Ultrasonically formation of supramolecular based ultrasound energy assisted solidification of floating organic drop microextraction for preconcentration of methadone in human plasma and saliva samples prior to gas chromatography–mass spectrometry

•A UA-SM-SFO-ME was developed as a green method for preconcentration of methadone.•Ultrasound energy enhance the extraction recovery of methadone as compared to vortex.•Ultrasonic caused the fast formation of supramolecular and dispersion of solvent.•Proper repeatability, low LOD and good linearity...

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Bibliographic Details
Published in:Ultrasonics sonochemistry 2019-01, Vol.50, p.182-187
Main Authors: Ezoddin, Maryam, Adlnasab, Laleh, kaveh, Akram afshari, Karimi, Mohammad Ali
Format: Article
Language:English
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Summary:•A UA-SM-SFO-ME was developed as a green method for preconcentration of methadone.•Ultrasound energy enhance the extraction recovery of methadone as compared to vortex.•Ultrasonic caused the fast formation of supramolecular and dispersion of solvent.•Proper repeatability, low LOD and good linearity were achieved in biological samples. In this work, an ultrasonic-assisted supramolecular based on solidification of floating organic drop microextraction (UA-SM-SFO-ME) was developed as a green method for preconcentration of methadone prior to gas chromatography–mass spectrometry (GC–MS). The supramolecular solvent aggregates containing reverse micelles of 1-dodecanol in tetrahydrofuran (THF) were formed by ultrasonication that subsequently dispersed in the sample solution. Ultrasonic waves caused the fast formation of supramolecular solvent aggregates. In this work, ultrasonication was used in two phases: First phase, the formation of reverse micelles and the second phase, the dispersion of supramolecular solvent in the sample solution. Actually, ultrasonication was basic of this presented work. In order to provide the highest extraction efficiency, the influence of various parameters on the method performance (supramolecular solvent type and volume, disperser solvent condition, pH, extraction time and salt concentration) was investigated. Based on the obtained optimum conditions, the limits of detection (LODs) and the limits of quantitation (LOQs) were obtained 0.5–1.2 µg L−1 and 1.2–2.5 µg L−1 with preconcentration factors in the range of 182–191, in water and biological samples, respectively. Subsequently, the method was assessed for preconcentration of the methadone in human plasma and saliva samples.
ISSN:1350-4177
1873-2828
DOI:10.1016/j.ultsonch.2018.09.019