Bisphenol A is one the most relevant endocrine disruptors for its toxicity and ubiquity in the environment, being largely employed as raw material for manufacturing processes of a wide number of compounds. Furthermore, bisphenol A is released in the drinking water when plastic-based bottles are incorrectly transported under sunlight, delivering contaminated drinking water. For the health of human beings and the environment, rapid and on site detection of bisphenol A in drinking water is an important issue. Herein, we report a novel and cost- effective printed electrochemical sensor for an enzymatic-free bisphenol A detection. This sensor encompasses the entire electrochemical cell printed on filter paper and the reagents for the measurement loaded in the cellulose fiber network, for delivering a reagent-free analytical tool. The working electrode was printed using ink modified with carbon black, a cost effective nanomaterial for sensitive and sustainable bisphenol A determi- nation. Several parameters including pH, frequency, and amplitude were optimized allowing for a detection limit of 0.03 μM with two linear ranges 0.1–0.9 μM and 1 μM–50 μM, using square wave voltammetry as electro- chemical technique. The satisfactory recovery values found in river and drinking water samples demonstrated the suitability of this sensor for screening analyses in water samples. These results revealed the attractiveness of this paper-based device thanks to the synergic combination of paper and carbon black as cost-effective materials.

Jemmeli, D., Marcoccio, E., Moscone, D., Dridi, C., Arduini, F. (2020). Highly sensitive paper-based electrochemical sensor for reagent free detection of bisphenol A. TALANTA, 216 [10.1016/j.talanta.2020.120924].

Highly sensitive paper-based electrochemical sensor for reagent free detection of bisphenol A

Moscone Danila;Arduini F.
2020-01-01

Abstract

Bisphenol A is one the most relevant endocrine disruptors for its toxicity and ubiquity in the environment, being largely employed as raw material for manufacturing processes of a wide number of compounds. Furthermore, bisphenol A is released in the drinking water when plastic-based bottles are incorrectly transported under sunlight, delivering contaminated drinking water. For the health of human beings and the environment, rapid and on site detection of bisphenol A in drinking water is an important issue. Herein, we report a novel and cost- effective printed electrochemical sensor for an enzymatic-free bisphenol A detection. This sensor encompasses the entire electrochemical cell printed on filter paper and the reagents for the measurement loaded in the cellulose fiber network, for delivering a reagent-free analytical tool. The working electrode was printed using ink modified with carbon black, a cost effective nanomaterial for sensitive and sustainable bisphenol A determi- nation. Several parameters including pH, frequency, and amplitude were optimized allowing for a detection limit of 0.03 μM with two linear ranges 0.1–0.9 μM and 1 μM–50 μM, using square wave voltammetry as electro- chemical technique. The satisfactory recovery values found in river and drinking water samples demonstrated the suitability of this sensor for screening analyses in water samples. These results revealed the attractiveness of this paper-based device thanks to the synergic combination of paper and carbon black as cost-effective materials.
2020
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/01 - CHIMICA ANALITICA
Settore CHEM-01/A - Chimica analitica
English
Con Impact Factor ISI
Carbon black; Nanomaterials; Square wave voltammetry; Microfluidic; River water; Drinking water
Jemmeli, D., Marcoccio, E., Moscone, D., Dridi, C., Arduini, F. (2020). Highly sensitive paper-based electrochemical sensor for reagent free detection of bisphenol A. TALANTA, 216 [10.1016/j.talanta.2020.120924].
Jemmeli, D; Marcoccio, E; Moscone, D; Dridi, C; Arduini, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/260413
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