Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples
Main Author: | |
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Publication Date: | 2011 |
Other Authors: | , , , , , |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10400.22/7753 |
Summary: | Prostate Cancer (PCa) is the most common form of cancer in men in Europe with a 61.4 % incidence among all cancer cases and a 12.1 % mortality [1] and, therefore, its early detection is fundamental for increasing the survival rate. Currently, diagnosis and management of patients with PCa is only based on the determination of the biomarker Prostate Specific Antigen (PSA). However, the method used for PCa detection has poor sensitivity and specificity, leading to false negative and false positive test results and many patients are sent to unnecessary biopsy procedures [2]. Therefore, there is a need to seek for new biomarkers and more effective screening. In this work, a biosensor device was developed for the quantification of sarcosine via electrochemical detection of H2O2 (at 0.6 V) generated from the catalyzed oxidation of sarcosine. The detection was carried out after the modification of carbon screen printed electrodes (SPEs) by immobilization of sarcosine oxidase (SOX) on the electrode surface. The strategies used herein included the activation of the carbon films by an electrochemical step and the formation of an NHS/EDAC layer to bond the enzyme to the electrode, the use of metallic or semiconductor nanoparticles layer previously or during the enzyme immobilization. In order to improve the sensor stability and selectivity a polymeric layer with extra enzyme content was further added. The proposed methodology for the detection of sarcosine allowed obtaining a limit of detection (LOD) of 1.6x10-5 mM, using a linear concentration range between 1x10-5 and 1x10-4 mM. The biosensor was successfully applied to the analysis of sarcosine in urine samples. |
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Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samplesProstate Cancer (PCa) is the most common form of cancer in men in Europe with a 61.4 % incidence among all cancer cases and a 12.1 % mortality [1] and, therefore, its early detection is fundamental for increasing the survival rate. Currently, diagnosis and management of patients with PCa is only based on the determination of the biomarker Prostate Specific Antigen (PSA). However, the method used for PCa detection has poor sensitivity and specificity, leading to false negative and false positive test results and many patients are sent to unnecessary biopsy procedures [2]. Therefore, there is a need to seek for new biomarkers and more effective screening. In this work, a biosensor device was developed for the quantification of sarcosine via electrochemical detection of H2O2 (at 0.6 V) generated from the catalyzed oxidation of sarcosine. The detection was carried out after the modification of carbon screen printed electrodes (SPEs) by immobilization of sarcosine oxidase (SOX) on the electrode surface. The strategies used herein included the activation of the carbon films by an electrochemical step and the formation of an NHS/EDAC layer to bond the enzyme to the electrode, the use of metallic or semiconductor nanoparticles layer previously or during the enzyme immobilization. In order to improve the sensor stability and selectivity a polymeric layer with extra enzyme content was further added. The proposed methodology for the detection of sarcosine allowed obtaining a limit of detection (LOD) of 1.6x10-5 mM, using a linear concentration range between 1x10-5 and 1x10-4 mM. The biosensor was successfully applied to the analysis of sarcosine in urine samples.REPOSITÓRIO P.PORTORebelo, Tânia S. C. R.Pereira, Carlos M.Sales, M. Goreti F.Noronha, João P.Costa-Rodrigues, JoãoSilva, FernandoFernandes, M. H.2016-02-26T16:19:00Z20112011-01-01T00:00:00Zconference objectinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10400.22/7753eng10.1016/j.aca.2014.08.005info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-07T10:32:32Zoai:recipp.ipp.pt:10400.22/7753Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T01:00:28.762699Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
title |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
spellingShingle |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples Rebelo, Tânia S. C. R. |
title_short |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
title_full |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
title_fullStr |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
title_full_unstemmed |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
title_sort |
Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples |
author |
Rebelo, Tânia S. C. R. |
author_facet |
Rebelo, Tânia S. C. R. Pereira, Carlos M. Sales, M. Goreti F. Noronha, João P. Costa-Rodrigues, João Silva, Fernando Fernandes, M. H. |
author_role |
author |
author2 |
Pereira, Carlos M. Sales, M. Goreti F. Noronha, João P. Costa-Rodrigues, João Silva, Fernando Fernandes, M. H. |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
REPOSITÓRIO P.PORTO |
dc.contributor.author.fl_str_mv |
Rebelo, Tânia S. C. R. Pereira, Carlos M. Sales, M. Goreti F. Noronha, João P. Costa-Rodrigues, João Silva, Fernando Fernandes, M. H. |
description |
Prostate Cancer (PCa) is the most common form of cancer in men in Europe with a 61.4 % incidence among all cancer cases and a 12.1 % mortality [1] and, therefore, its early detection is fundamental for increasing the survival rate. Currently, diagnosis and management of patients with PCa is only based on the determination of the biomarker Prostate Specific Antigen (PSA). However, the method used for PCa detection has poor sensitivity and specificity, leading to false negative and false positive test results and many patients are sent to unnecessary biopsy procedures [2]. Therefore, there is a need to seek for new biomarkers and more effective screening. In this work, a biosensor device was developed for the quantification of sarcosine via electrochemical detection of H2O2 (at 0.6 V) generated from the catalyzed oxidation of sarcosine. The detection was carried out after the modification of carbon screen printed electrodes (SPEs) by immobilization of sarcosine oxidase (SOX) on the electrode surface. The strategies used herein included the activation of the carbon films by an electrochemical step and the formation of an NHS/EDAC layer to bond the enzyme to the electrode, the use of metallic or semiconductor nanoparticles layer previously or during the enzyme immobilization. In order to improve the sensor stability and selectivity a polymeric layer with extra enzyme content was further added. The proposed methodology for the detection of sarcosine allowed obtaining a limit of detection (LOD) of 1.6x10-5 mM, using a linear concentration range between 1x10-5 and 1x10-4 mM. The biosensor was successfully applied to the analysis of sarcosine in urine samples. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011 2011-01-01T00:00:00Z 2016-02-26T16:19:00Z |
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conference object |
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info:eu-repo/semantics/publishedVersion |
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http://hdl.handle.net/10400.22/7753 |
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http://hdl.handle.net/10400.22/7753 |
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eng |
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eng |
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10.1016/j.aca.2014.08.005 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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