dc.contributorCSIC
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:19:54Z
dc.date.accessioned2022-10-05T16:02:44Z
dc.date.available2014-05-20T15:19:54Z
dc.date.available2022-10-05T16:02:44Z
dc.date.created2014-05-20T15:19:54Z
dc.date.issued1998-04-01
dc.identifierAnalusis. Les Ulis Cedexa: E D P Sciences, v. 26, n. 3, p. 130-134, 1998.
dc.identifier0365-4877
dc.identifierhttp://hdl.handle.net/11449/31290
dc.identifier10.1051/analusis:1998122
dc.identifierWOS:000073612000015
dc.identifierWOS000073612000015.pdf
dc.identifier4148837403618207
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3904082
dc.description.abstractEnzyme-Linked Immunosorbent Assay (ELISA) has been evaluated by analyzing rich-humic water samples from tropical rivers. The samples were spiked with atrazine at ppb level Different pHs (4 to 9) and humic concentrations (2.5 to 40 mg L-1) were investigated. The assay performance showed a strong dependence on the pH values and amount of humic matter at low atrazine concentration. From all the conditions studied the low pH (pH 4) and high humic substances concentrations (40 mg L-1) showed the greatest influence. The IC50 value to control sample (no humic) diminished from 0.28 nmol L-1 to 0.64 nmol L-1 to humic acid solution. This effect is specially noted for the humic acid fractions, since fulvic acid fractions showed no significant change on the immunoassay results. Additionally, it has been demonstrated that at basic pH the matrix effect produced by the natural Brazilian water sample containing humic substances even at 40 mg L-1 disappears. Therefore, the ELISA method used to determine atrazine, can be employed to determine this pesticide in water samples containing humic substances without prior preparation.
dc.languageeng
dc.publisherE D P Sciences
dc.relationAnalusis
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectatrazine
dc.subjectaquatic humic substances
dc.subjectimmunoassays
dc.titleAtrazine interaction with tropical humic substances by Enzyme Linked Immunosorbent Assay
dc.typeArtigo


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