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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1997-11-26
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pubmed:abstractText |
Leachate and soil samples collected from different tillage systems were analyzed for atrazine using gas chromatography (GC) and an enzyme-linked immunosorbent assay (ELISA) based on magnetic particle technology. Solid-phase extraction (SPE) was used to concentrate atrazine residues in leachate samples and soil extracts before GC analysis. Atrazine concentrations determined by GC ranged from 0.1 to 600 micrograms L-1 for water samples and from 1.0 to 700 micrograms kg-1 for soil samples. Atrazine concentrations in 92 leachate samples as determined by ELISA were well-correlated (R = 0.97) with GC levels over the entire concentration range. Soil samples (215) were prepared and analyzed by three combinations of extraction/detection methods: 1) conventional extraction for GC/detection by GC analysis; 2)conventional extraction for GC/detection by ELISA analysis; 3)extraction for ELISA using a commercially available field kit/detection by ELISA analysis. Methanol (MeOH) in water was the common extractant. Although the initial comparison of soil extracts between the two different systems (Method 1 versus Method 3) was favorable (R = 0.97), two-thirds of the samples contained levels below the lower threshold for atrazine detection by both methods and some extracts were perceived to provide unfavorable substrate conditions (> 10% MeOH). Elimination of these data points reduced the correlation value (R = 0.77). To determine possible sources of variability, the extraction and detection methods were examined separately. In a comparison of extraction methods (Method 2 versus Method 3), ELISA analysis of kit extracts underestimated (R = 0.71) atrazine levels compared to those conventionally extracted, suggesting that differences in extraction time between methods may have accounted for reduced kit efficiency. Where detection methods (Method 1 versus Method 2) were compared on specific extracts (< 10% MeOH), good agreement (R = 0.99) was achieved between ELISA and GC values, illustrating that control of extractant concentration is critical in using this assay for atrazine detection in soil.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Atrazine,
http://linkedlifedata.com/resource/pubmed/chemical/Herbicides,
http://linkedlifedata.com/resource/pubmed/chemical/Pesticide Residues,
http://linkedlifedata.com/resource/pubmed/chemical/Soil Pollutants,
http://linkedlifedata.com/resource/pubmed/chemical/Water Pollutants, Chemical
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0360-1234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
32
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
845-60
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pubmed:dateRevised |
2009-7-21
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pubmed:meshHeading |
pubmed-meshheading:9350076-Atrazine,
pubmed-meshheading:9350076-Chromatography, Gas,
pubmed-meshheading:9350076-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:9350076-Herbicides,
pubmed-meshheading:9350076-Pennsylvania,
pubmed-meshheading:9350076-Pesticide Residues,
pubmed-meshheading:9350076-Soil Pollutants,
pubmed-meshheading:9350076-Water Pollutants, Chemical
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pubmed:year |
1997
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pubmed:articleTitle |
Comparison of gas chromatography and immunoassay methods for the detection of atrazine in water and soil.
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pubmed:affiliation |
Dept. of Agronomy, Pennsylvania State University, University Park 16802, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study
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