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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
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 (p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780943/ https://www.ncbi.nlm.nih.gov/pubmed/31540212 http://dx.doi.org/10.3390/polym11091497 |
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author | Moczko, Ewa Díaz, Richard Rivas, Bernabé García, Camilo Pereira, Eduardo Piletsky, Sergey Cáceres, César |
author_facet | Moczko, Ewa Díaz, Richard Rivas, Bernabé García, Camilo Pereira, Eduardo Piletsky, Sergey Cáceres, César |
author_sort | Moczko, Ewa |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6780943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67809432019-10-30 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 Polymers (Basel) Article 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. MDPI 2019-09-13 /pmc/articles/PMC6780943/ /pubmed/31540212 http://dx.doi.org/10.3390/polym11091497 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Moczko, Ewa Díaz, Richard Rivas, Bernabé García, Camilo Pereira, Eduardo Piletsky, Sergey Cáceres, César Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title | Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title_full | Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title_fullStr | Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title_full_unstemmed | Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title_short | Molecularly Imprinted Nanoparticles Assay (MINA) in Pseudo ELISA: An Alternative to Detect and Quantify Octopamine in Water and Human Urine Samples |
title_sort | molecularly imprinted nanoparticles assay (mina) in pseudo elisa: an alternative to detect and quantify octopamine in water and human urine samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6780943/ https://www.ncbi.nlm.nih.gov/pubmed/31540212 http://dx.doi.org/10.3390/polym11091497 |
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