CSIRO Publishing Books Journals About Us Shopping Cart You are here: Journals > Environmental Chemistry   
Environmental Chemistry
  Environmental problems - Chemical approaches
 
Search
 
 
  Advanced Search
   

Journal Home
About the Journal
Editorial Boards
Contacts
Content
Online Early
Current Issue
Just Accepted
All Issues
Special Issues
Research Fronts
Sample Issue
Covers
For Authors
General Information
Notice to Authors
Submit Article
Open Access
For Referees
General Information
Review Article
Annual Referee Index
For Subscribers
Subscription Prices
Customer Service

 Early Alert
Subscribe to our email Early Alert or RSS feeds for the latest journal papers.

 Connect with us
facebook   youtube

 

Article << Previous     |     Next >>   Contents Vol 2(3)

High Throughput Determination of BTEX by a One-Step Fluorescence Polarization Immunoassay

Sergei A. Eremin A D, Dietmar Knopp B, Reinhard Niessner B, Ji Youn Hong C, Song-Ja Park C, Myung Ja Choi C

A Faculty of Chemistry, Moscow State University, Leninsky Gory 1, Moscow 119992, Russia.
B Institute of Hydrochemistry and Chemical Balneology, Technical University of Munich, 81377 München, Germany.
C Bioanalysis and Biotransformation Research Centre, Korea Institute of Science and Technology, Cheongryang Seoul 130-650, Seoul, Korea.
D Corresponding author. Email: eremin@enz.chem.msu.ru
 
PDF (229 KB) $25
 Export Citation
 Print
  

Environmental Context. Benzene, toluene, ethylbenzene, and xylenes (BTEX) are used as solvents in paints and coatings and are constituents of petroleum products. BTEX can contaminate air, water or soil and is toxic; benzene, in particular, is a recognized human carcinogen. Most existing methods for detecting BTEX are time-consuming, complicated and very expensive for routine screening. A rapid immunoassay of BTEX is presented that greatly simplifies environmental monitoring of water contamination.

Abstract. For the rapid screening of BTEX (benzene, toluene, ethylbenzene, xylenes), a fluorescence polarization immunoassay (FPIA) was developed using the fluorescence polarization analyzer Abbott TDx. Several fluorescence-labelled tracers were synthesized by binding ethylenediamine fluorescein thiocarbamyl (EDF) to various substituted phenylcarboxylic acids. The binding of 27 tracers with two antisera that can be considered as class-specific for BTEX was investigated to select optimal tracer–antibody pairs. Significant differences were found in binding, titer, sensitivity, and assay kinetics. A best pair of anti-BTEX antiserum and EDF-labelled p-tolylacetic acid tracer was selected for FPIA. To simplify the method, an immunocomplex single reagent was prepared to detect BTEX by a one-step FPIA. One-step FPIA is a rapid homogeneous type of immunoassay that has only one pipetting step, does not need separation of free and bound analyte and can be performed at room temperature. The within-run coefficient of variation was ranged between 3.4% and 5.7%. Furthermore, if the measurement can be done at constant temperature, standards for every assay run are unnecessary. Cross-reactivity studies of petroleum compounds and a BTEX mixture indicated that p-xylene was most reactive with a limit of detection (LOD) of 0.22 µg mL-1 in 50 µL of sample. The LOD for toluene and benzene was 2.1 and 11 µg mL-1 respectively. The immunocomplex single reagent has proven to be significantly more stable than the corresponding solutions of antibody and tracer.

Keywords: immunoassay — BTEX — immunodetection


   
Subscriber Login
Username:
Password:  

    


 
Top  Email this page
 
Legal & Privacy | Contact Us | Help

CSIRO

© CSIRO 1996-2012