Ethinylestradiol quantification in drinking water sources using a fluorescent paper based immunosensor
Autor: | Julio Raba, Rudolf J. Schneider, Galo J. A. A. Soler-Illia, Eduardo A. Takara, Mara Alderete, Germán A. Messina, María L. Scala-Benuzzi |
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Rok vydání: | 2018 |
Předmět: |
02 engineering and technology
01 natural sciences Horseradish peroxidase Analytical Chemistry Catalysis purl.org/becyt/ford/1 [https] Ethinylestradiol purl.org/becyt/ford/1.4 [https] medicine ETHINYLESTRADIOL Spectroscopy LED-INDUCED FLUORESCENCE Detection limit Wax Chromatography Filter paper biology medicine.diagnostic_test Chemistry 010401 analytical chemistry Ciencias Químicas PAPER BASED DEVICES 021001 nanoscience & nanotechnology Fluorescence AMINO-FUNCTIONALIZED MESOPOROUS SILICA PARTICLES 0104 chemical sciences visual_art Immunoassay biology.protein visual_art.visual_art_medium Química Analítica 0210 nano-technology CIENCIAS NATURALES Y EXACTAS medicine.drug |
Zdroj: | CONICET Digital (CONICET) Consejo Nacional de Investigaciones Científicas y Técnicas instacron:CONICET |
ISSN: | 0026-265X |
DOI: | 10.1016/j.microc.2018.05.038 |
Popis: | In this work we report a novel paper-based analytical device read-out via LED-induced fluorescence detection (FPAD) for the quantification of the emerging pollutant ethinylestradiol (EE2) in river water samples. The PAD was used as a reaction platform for a competitive enzyme immunoassay. For the PAD development, microzones of filter paper, printed by a wax printing method, were modified with amino-functionalized SBA-15 and subsequently, anti-EE2 specific antibodies were covalently immobilized. The determination of EE2 in water was carried out by adding a fixed concentration of EE2 conjugated with the enzyme horseradish peroxidase (HRP) to samples and standards. Then, the FPAD were added and incubated for 10 min. Finally, the detection was performed by the reaction of 10-acetyl-3,7-dihydroxyphenoxazine (ADHP) whose oxidation is catalyzed by HRP in the presence of H2O2, obtaining the highly fluorescent resorufin (R). Resorufin was detected by LED excitation at 550 nm, observing emission at 585 nm. The EE2 concentration in the samples was inversely proportional to the relative fluorescence obtained from the enzymatic reaction products. The FPAD assay showed a detection limit (LOD) of 0.05 ng L−1 and coefficients of variation (CV) below 4.5% within-assay and below 6.5% between-assay, respectively. The results obtained show the potential suitability of our FPAD for the selective and sensitive quantification of EE2 in river water samples. In addition, it has the PADs advantages of being disposable, easy to apply and inexpensive. Fil: Scala Benuzzi, María Luz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina Fil: Takara, Eduardo Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina Fil: Alderete, Mara. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina Fil: Soler Illia, Galo Juan de Avila Arturo. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina Fil: Schneider, Rudolf J.. Bundesanstalt für Materialforschung und -prüfung; Alemania Fil: Raba, Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina Fil: Messina, Germán Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina |
Databáze: | OpenAIRE |
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