Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractNeedle microextraction trap for on-site analysis of airborne volatile compounds at ultra-trace levels in gaseous samples    Next AbstractEvaluation of matrix effects in the analysis of volatile organic compounds in whole blood with solid-phase microextraction »

J Chromatogr A


Title:A headspace needle-trap method for the analysis of volatile organic compounds in whole blood
Author(s):Alonso M; Castellanos M; Besalu E; Sanchez JM;
Address:"Department of Chemistry, University of Girona, Campus Montilivi s/n, 17071 Girona, Spain"
Journal Title:J Chromatogr A
Year:2012
Volume:20120701
Issue:
Page Number:23 - 30
DOI: 10.1016/j.chroma.2012.06.083
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"Needle trap devices (NTDs) are a relatively new and promising tool for headspace (HS) analysis. In this study, a dynamic HS sampling procedure is evaluated for the determination of volatile organic compounds (VOCs) in whole blood samples. A full factorial design was used to evaluate the influence of the number of cycles and incubation time and it is demonstrated that the controlling factor in the process is the number of cycles. A mathematical model can be used to determine the most appropriate number of cycles required to adsorb a prefixed amount of VOCs present in the HS phase whenever quantitative adsorption is reached in each cycle. Matrix effect is of great importance when complex biological samples, such as blood, are analyzed. The evaluation of the salting out effect showed a significant improvement in the volatilization of VOCs to the HS in this type of matrices. Moreover, a 1:4 (blood:water) dilution is required to obtain quantitative recoveries of the target analytes when external calibration is used. The method developed gives detection limits in the 0.020-0.080mug L(-1) range (0.1-0.4mug L(-1) range for undiluted blood samples) with appropriate repeatability values (RSD<15% at high level and <23% at LOQ level). Figure of merits of the method can be improved by using a smaller phase ratio (i.e., an increase in the blood volume and a decrease in the HS volume), which lead to lower detection limits, better repeatability values and greater sensibility. Twenty-eight blood samples have been evaluated with the proposed method and the results agree with those indicated in other studies. Benzene was the only target compound that gave significant differences between blood levels detected in volunteer non-smokers and smokers"
Keywords:Adsorption Analysis of Variance Benzene Derivatives/blood/isolation & purification Blood Chemical Analysis/*instrumentation/methods Furans/blood/isolation & purification Gas Chromatography-Mass Spectrometry/*instrumentation/methods Humans Limit of Detecti;
Notes:"MedlineAlonso, Monica Castellanos, Mar Besalu, Emili Sanchez, Juan M eng Research Support, Non-U.S. Gov't Netherlands 2012/07/17 J Chromatogr A. 2012 Aug 24; 1252:23-30. doi: 10.1016/j.chroma.2012.06.083. Epub 2012 Jul 1"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 21-09-2024