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Updated: Dec 8, 2025

A Lipid Extraction and Analysis Method for Characterizing Soil Microbes in Experiments with Many Samples
Published on: July 16, 2017
Amine/phenyl gradient derived base layer as a comprehensive extractive phase for headspace cooled in-tube
Marzieh Enteshari Najafabadi1, Habib Bagheri1, Akram Rostami2
1Environmental and Bio-Analytical Laboratories, Department of Chemistry Sharif University of Technology, P.O. Box 11365-9516, Tehran, Iran.
Abstract:
A gradient derived base layer extractive phase was synthesized and applied for the determination of volatile organic compounds (VOCs) in saliva samples using the headspace cooled in-tube microextraction (HS-CITME) method. The base layers from three different sols of phenyltriethoxysilane (PTES), octyltrimethoxysilane (OTMS) and methyltrimethoxysilane (MTMS) as nonpolar precursors were individually dip coated on the stainless steel wires (SSW). Then, the hydrolyzed polar precursor aminopropyltriethoxysilane (APTES) reacted with the silanol groups already formed on the surface of SSWs via controlled rate infusion (CRI) method. The presence of polar and non-polar functional groups on the surface of substrate was evaluated by Fourier-transform infrared spectroscopy (FTIR) while the morphology and thickness of the most suitable gradient coating (amine/phenyl) were also investigated by scanning electron microscopy (SEM). Assessment of the gradient extractive phase efficiency was carried out determining a group of VOCs with different polarities coupled with gas chromatography-mass spectrometry (GCMS) and the improved performance of the synthesized base layer coatings was observed. Furthermore, a cooling device was designed and implemented to the extracting system to improve the efficiency by influencing the exothermic nature of process. The data were analyzed by principal component analysis (PCA), and hierarchical cluster analysis (HCA) and the results were interpreted by polarities of analytes. Finally, under the optimized conditions, the limits of detection (LOD) and limits of quantification (LOQ) were 0.15 and 0.50 ng L-1, respectively. The intra-day and inter-day relative standard deviations (RSDs) at 5 and 50 ng L-1 (n = 3) using a single extractive phase were 2-6 and 10-17, respectively. The data associated with RSDs% for three extractive phases were between 16 and 19 %. Eventually, the method was conveniently applied to the extraction of VOCs from saliva samples of smokers and satisfactory relative recoveries (RR%) (95-108 %) were achieved and low quantities of VOCs were detected.
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