Determination of four benzodiazepine residues in pork using multiwalled carbon nanotube solid-phase extraction and gas chromatography–mass spectrometry

• Published in: Journal of Chromatography A Vol. 1136; no. 1; pp. 99 - 105
• Main Authors: Wang, Liping, Zhao, Haixiang, Qiu, Yueming, Zhou, Zhiqiang
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 08.12.2006; Elsevier
• Subjects: Adsorption; Animals; Benzodiazepines; Benzodiazepines - analysis; Biological and medical sciences; Calibration; Carbon - chemistry; Drug Residues - analysis; Food industries; Fundamental and applied biological sciences. Psychology; Gas Chromatography-Mass Spectrometry - methods; GC–MS; Meat and meat product industries; Meat Products - analysis; Multiwalled carbon nanotubes; Nanostructures; Pork; Reproducibility of Results; Sensitivity and Specificity; Solid-phase extraction; Swine; Multiwalled carbon nanotubes; GC–MS; Solid-phase extraction; Benzodiazepines; Pork; Solid phase extraction; Chemical analysis; Psychotropic; Carbon nanotubes; Anticonvulsant; Chemical enrichment; Sample preparation; Triazolam; Benzodiazepine derivatives; Sedative; Adsorbent; Diazepam; Quantitative analysis; Trace analysis; Coupled method; Hypnotic; Alprazolam; GC-MS; Gas chromatography; Tranquillizer; Multiwalled nanotube; Estazolam; Residue; Mass spectrometry; Chemical contamination
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2006.09.088

A solid-phase extraction (SPE)/GC–MS method using multiwalled carbon nanotubes (MWCNTs) was developed for the determination of four benzodiazepine residues including diazepam, estazolam, alprazolam and triazolam in pork. The analytes were extracted by ultrasonic assistant extraction using acetonitrile, concentrated and purified by MWCNTs packed cartridge, and determined by GC–MS. Ultrasonic extraction conditions, which included temperature, time, power, and solvent volume, were optimized. Comparative studies showed that MWCNTs were superior to C18 for the adsorption of drugs. Parameters influencing SPE efficiency, such as sample amounts, variety and volume of the eluent, were also optimized. Electron ionization (EI) operating in time program-selected ion monitoring mode (SIM) was used for GC–MS identification. The analytes were quantified with external standard calibration curve method. Lower limit of detection and quantification was obtained by the new method. Linear calibration curves were obtained in the concentration range from 10 ng/mL to 500 ng/mL for diazepam and from 20 ng/mL to 1000 ng/mL for estazolam, alprazolam and triazolam with calibration coefficients of 0.99 and above. The average recoveries for the four benzodiazepines spiked in pork were 75% to 104% and their relative standard deviations were between 1.3% and 10%. The limits of detection were 2 μg/kg for diazepam and 5 μg/kg for estazolam, alprazolam and triazolam in pork, respectively.