Electrochemical Approach to Detection of Chlorophene in Water Catalyzed by a Laccase Modified Gold Electrode
Gabriela Elizabeth Quintanilla-Villanueva,
Donato Luna-Moreno,
Araceli Sánchez-Álvarez,
Juan Francisco Villarreal-Chiu,
José Manuel Rodríguez-Delgado,
Melissa Marlene Rodríguez-Delgado
Affiliations
Gabriela Elizabeth Quintanilla-Villanueva
Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Laboratorio de Biotecnología, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza 66455, Nuevo León, Mexico
Donato Luna-Moreno
Centro de Investigaciones en Óptica AC, Div. de Fotónica, Loma del Bosque 115, Col. Lomas del Campestre, León 37150, Guanajuato, Mexico
Araceli Sánchez-Álvarez
Universidad Tecnológica de León, Electromecánica Industrial, Blvd. Universidad Tecnológica #225, Col. San Carlos, León 37670, Guanajuato, Mexico
Juan Francisco Villarreal-Chiu
Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Laboratorio de Biotecnología, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza 66455, Nuevo León, Mexico
José Manuel Rodríguez-Delgado
Tecnológico de Monterrey, School of Engineering and Sciences, Av. Eugenio Garza Sada Sur No. 2501, Col. Tecnológico, Monterrey 64849, Nuevo León, Mexico
Melissa Marlene Rodríguez-Delgado
Universidad Autónoma de Nuevo León, Facultad de Ciencias Químicas, Laboratorio de Biotecnología, Av. Universidad S/N Ciudad Universitaria, San Nicolás de los Garza 66455, Nuevo León, Mexico
Despite the increasing number of reports that relate antimicrobial chlorophene (CP) with health and environmental effects, few studies have addressed biosensing technologies to detect this threat. This work proposed an electrochemical approach for the detection of CP using laccase enzymes as an alternative recognition element immobilized onto thin-film gold electrodes. The electrochemical parameters of the detection method, under controlled conditions, resulted in a limit of detection (0.14 ± 0.06 mg L−1) and quantification (0.48 ± 0.04 mg L−1) that agreed with concentrations of CP that already had been measured in natural water samples. Nevertheless, during the analysis of natural river water samples, the provided method suffered a drawback due to matrix effects reflected in the obtained recovery percentage, the value of which was 62.0 ± 2.4% compared to the 101.3 ± 3.5% obtained by the HPLC reference method. These detrimental effects were mainly attributed to organic matter, SO4-2, and Cl- present in river samples.