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 AbstractBioconcentration factors for volatile organic compounds in vegetation    Next AbstractBehavioral responses of western corn rootworm larvae to volatile semiochemicals from corn seedlings »

J Chromatogr A


Title:Internal standards: a source of analytical bias for volatile organic analyte determinations
Author(s):Hiatt MH;
Address:"U.S. Environmental Protection Agency, National Exposure Research Laboratory, Environmental Sciences Division, P.O. Box 93478, Las Vegas, NV 89193-3478, USA. hiatt.mike@epa.gov"
Journal Title:J Chromatogr A
Year:2011
Volume:20101205
Issue:3
Page Number:498 - 503
DOI: 10.1016/j.chroma.2010.11.078
ISSN/ISBN:1873-3778 (Electronic) 0021-9673 (Linking)
Abstract:"The use of internal standards in the determination of volatile organic compounds as described in SW-846 Method 8260C introduces a potential for bias in results once the internal standards (ISTDs) are added to a sample for analysis. The bias is relative to the dissimilarity between the analyte and internal standard physical properties that influence how easily analytes are separated from a matrix and concentrated during analysis. Method 5032 is a vacuum distillation procedure for extracting analytes from a sample for use with Method 8260C. Vacuum distillation is also incorporated within another GC/MS analytical procedure, Method 8261A. Method 8260C/5032 and Method 8261A are experimentally identical, however, Method 8261A uses internal standards differently by relating the recovery of each compound to its boiling point and relative volatility. By processing each analysis (water, soil, and biota) using both Method 8260C and Method 8261A, the two approaches are compared on the basis of analyte bias and the failure rate of the quality controls. Analytes were grouped by how similar their boiling points and natural log of their relative volatilities (lnRVs) were to their Method 8260C recommended ISTDs. For the most similar analytes, the Method 8260C determinations yielded an average bias less than 10% and a failure to meet calibration criteria less than 7%. However, as the difference between analyte and ISTD became greater the bias increased to over 40% (matrix dependent) and its calibration failure rate approached 70%. In comparison, when the Method 8260C data were reprocessed as Method 8261A determinations, this trend for groupings was minimized with biases increasing from 6% to only 20% and the calibration failure rate went from 0% to 15%"
Keywords:Calibration Distillation Gas Chromatography-Mass Spectrometry/*standards Reference Standards Soil/chemistry Volatile Organic Compounds/*analysis/chemistry Water/chemistry;
Notes:"MedlineHiatt, Michael H eng Comparative Study Netherlands 2010/12/24 J Chromatogr A. 2011 Jan 21; 1218(3):498-503. doi: 10.1016/j.chroma.2010.11.078. Epub 2010 Dec 5"

 
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 26-12-2024