Sarcosine oxidase composite screen-printed electrode for sarcosine determination in biological samples

Bibliographic Details
Main Author: Rebelo, Tânia S. C. R.
Publication Date: 2011
Other Authors: Pereira, Carlos M., Sales, M. Goreti F., Noronha, João P., Costa-Rodrigues, João, Silva, Fernando, Fernandes, M. H.
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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spelling 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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