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Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples.
Moczko, Ewa; Díaz, Richard; Rivas, Bernabé; García, Camilo; Pereira, Eduardo; Piletsky, Sergey; Cáceres, César.
Afiliação
  • Moczko E; Departamento de Química Ambiental, Facultad de Ciencias, Universidad Católica de la Santísima Concepción, Concepción 4090541, Chile. ewa@ucsc.cl.
  • Díaz R; Departamento de Polímeros, Facultad de Ciencias Químicas, Universidad de Concepción, Concepción 4070371, Chile. richdiaz@udec.cl.
  • Rivas B; Departamento de Polímeros, Facultad de Ciencias Químicas, Universidad de Concepción, Concepción 4070371, Chile. brivas@udec.cl.
  • García C; Departamento de Ciencias Biológicas y Químicas, Facultad de Recursos Naturales, Universidad Católica de Temuco, Temuco 4781312, Chile. cgarcia@uct.cl.
  • Pereira E; Departamento de Química Analítica e Inorgánica, Facultad de Ciencias Químicas, Universidad de Concepción, Concepción 4070371, Chile. epereira@udec.cl.
  • Piletsky S; Chemistry Department, College of Science and Engineering, University of Leicester, Leicester LE1 7RH, UK. sp523@leicester.ac.uk.
  • Cáceres C; Departamento de Polímeros, Facultad de Ciencias Químicas, Universidad de Concepción, Concepción 4070371, Chile. cecaceres@udec.cl.
Polymers (Basel) ; 11(9)2019 Sep 13.
Article em En | MEDLINE | ID: mdl-31540212
In 2004, octopamine was added to the list of drugs banned by the world anti-doping agency (WADA) and prohibited in any sport competition. This work aims to develop a new analytical method to detect octopamine in water and human urine samples. We proposed a pseudo-enzyme-linked immunosorbent assay (pseudo-ELISA) by replacing traditional monoclonal antibodies with molecularly imprinted polymer nanoparticles (nanoMIPs). NanoMIPs were synthesised by a solid-phase approach using a persulfate initiated polymerisation in water. Their performance was analysed in pseudo competitive ELISA based on the competition between free octopamine and octopamine-HRP conjugated. The final assay was able to detect octopamine in water within the range 1 nmol·L-1-0.1 mol·L-1 with a detection limit of 0.047 ± 0.00231 µg·mL-1 and in human urine samples within the range 1 nmol·L-1-0.0001 mol·L-1 with a detection limit of 0.059 ± 0.00281 µg·mL-1. In all experiments, nanoMIPs presented high affinity to the target molecules and almost no cross-reactivity with analogues of octopamine such as pseudophedrine or l-Tyrosine. Only slight interference was observed from the human urine matrix. The high affinity and specificity of nanoMIPs and no need to maintain a cold chain logistics makes the nanoMIPs a competitive alternative to antibodies. Furthermore, this work is the first attempt to use nanoMIPs in pseudo-ELISA assays to detect octopamine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Polymers (Basel) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Chile País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Polymers (Basel) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Chile País de publicação: Suíça