Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos

En este trabajo de grado se desarrolló un biosensor amperométrico utilizando electrodos serigrafiados de oro que fueron modificados con nanotubos de difenilalanina, glutaraldehído como agente entrecruzante y peroxidasa de palma real como agente de reconocimiento biológico para la detección de peróxi...

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Autores:
Vargas Ramirez, Jesus Alberto
Tipo de recurso:
http://purl.org/coar/version/c_b1a7d7d4d402bcce
Fecha de publicación:
2016
Institución:
Universidad Industrial de Santander
Repositorio:
Repositorio UIS
Idioma:
spa
OAI Identifier:
oai:noesis.uis.edu.co:20.500.14071/34941
Acceso en línea:
https://noesis.uis.edu.co/handle/20.500.14071/34941
https://noesis.uis.edu.co
Palabra clave:
Biosensor
Peroxidasa De Palma Real
Electrodo De Oro
Nanotubos De Péptidos.
In this work we developed a novel amperometric hydrogen peroxide biosensor based on the interaction of royal palm peroxidase (Roystonea regia) and peptide nanotubes by using glutaraldehyde as a linker on gold screen printed electrode. The development of the enzyme electrode consisted in four steps. The first step was the extraction and semi-purification of the peroxidase from royal palm tree. This process allowed to increase the specific activity and purification factor to 504.34 U / mg and 6.5 respectively. Then the electrode surface was modified with royal palm peroxidase by using peptide nanotube and glutaraldehyde
which allowed the electronic communication between the enzyme and the electrode surface. This step allowed the adsorption of peroxidase on the electrode surface. Bioelectrocatalytic reduction of hydrogen peroxide is observed at a redox potential -0.4 V vs Ag. This fact was demonstrated by the increasing on the electrocatalytic current of reduction at different concentrations of hydrogen peroxide. It was found that the electron transfer process was controlled superficially and depended on the pH of the solution. Based on the results from cronoamperometry
the enzyme electrode showed a linear response to hydrogen peroxide over a concentration range from 500 µM to 6000 µM with a detection limit of 432.71 µM and a sensibility of 0.024.
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Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
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dc.title.none.fl_str_mv Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
dc.title.english.none.fl_str_mv Biosensor, Royal Palm Peroxidase, Gold Screen Printed Electrode, Peptide Nanotubes.
title Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
spellingShingle Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
Biosensor
Peroxidasa De Palma Real
Electrodo De Oro
Nanotubos De Péptidos.
In this work we developed a novel amperometric hydrogen peroxide biosensor based on the interaction of royal palm peroxidase (Roystonea regia) and peptide nanotubes by using glutaraldehyde as a linker on gold screen printed electrode. The development of the enzyme electrode consisted in four steps. The first step was the extraction and semi-purification of the peroxidase from royal palm tree. This process allowed to increase the specific activity and purification factor to 504.34 U / mg and 6.5 respectively. Then the electrode surface was modified with royal palm peroxidase by using peptide nanotube and glutaraldehyde
which allowed the electronic communication between the enzyme and the electrode surface. This step allowed the adsorption of peroxidase on the electrode surface. Bioelectrocatalytic reduction of hydrogen peroxide is observed at a redox potential -0.4 V vs Ag. This fact was demonstrated by the increasing on the electrocatalytic current of reduction at different concentrations of hydrogen peroxide. It was found that the electron transfer process was controlled superficially and depended on the pH of the solution. Based on the results from cronoamperometry
the enzyme electrode showed a linear response to hydrogen peroxide over a concentration range from 500 µM to 6000 µM with a detection limit of 432.71 µM and a sensibility of 0.024.
title_short Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
title_full Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
title_fullStr Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
title_full_unstemmed Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
title_sort Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidos
dc.creator.fl_str_mv Vargas Ramirez, Jesus Alberto
dc.contributor.advisor.none.fl_str_mv Castillo León, John Jairo
dc.contributor.author.none.fl_str_mv Vargas Ramirez, Jesus Alberto
dc.subject.none.fl_str_mv Biosensor
Peroxidasa De Palma Real
Electrodo De Oro
Nanotubos De Péptidos.
topic Biosensor
Peroxidasa De Palma Real
Electrodo De Oro
Nanotubos De Péptidos.
In this work we developed a novel amperometric hydrogen peroxide biosensor based on the interaction of royal palm peroxidase (Roystonea regia) and peptide nanotubes by using glutaraldehyde as a linker on gold screen printed electrode. The development of the enzyme electrode consisted in four steps. The first step was the extraction and semi-purification of the peroxidase from royal palm tree. This process allowed to increase the specific activity and purification factor to 504.34 U / mg and 6.5 respectively. Then the electrode surface was modified with royal palm peroxidase by using peptide nanotube and glutaraldehyde
which allowed the electronic communication between the enzyme and the electrode surface. This step allowed the adsorption of peroxidase on the electrode surface. Bioelectrocatalytic reduction of hydrogen peroxide is observed at a redox potential -0.4 V vs Ag. This fact was demonstrated by the increasing on the electrocatalytic current of reduction at different concentrations of hydrogen peroxide. It was found that the electron transfer process was controlled superficially and depended on the pH of the solution. Based on the results from cronoamperometry
the enzyme electrode showed a linear response to hydrogen peroxide over a concentration range from 500 µM to 6000 µM with a detection limit of 432.71 µM and a sensibility of 0.024.
dc.subject.keyword.none.fl_str_mv In this work we developed a novel amperometric hydrogen peroxide biosensor based on the interaction of royal palm peroxidase (Roystonea regia) and peptide nanotubes by using glutaraldehyde as a linker on gold screen printed electrode. The development of the enzyme electrode consisted in four steps. The first step was the extraction and semi-purification of the peroxidase from royal palm tree. This process allowed to increase the specific activity and purification factor to 504.34 U / mg and 6.5 respectively. Then the electrode surface was modified with royal palm peroxidase by using peptide nanotube and glutaraldehyde
which allowed the electronic communication between the enzyme and the electrode surface. This step allowed the adsorption of peroxidase on the electrode surface. Bioelectrocatalytic reduction of hydrogen peroxide is observed at a redox potential -0.4 V vs Ag. This fact was demonstrated by the increasing on the electrocatalytic current of reduction at different concentrations of hydrogen peroxide. It was found that the electron transfer process was controlled superficially and depended on the pH of the solution. Based on the results from cronoamperometry
the enzyme electrode showed a linear response to hydrogen peroxide over a concentration range from 500 µM to 6000 µM with a detection limit of 432.71 µM and a sensibility of 0.024.
description En este trabajo de grado se desarrolló un biosensor amperométrico utilizando electrodos serigrafiados de oro que fueron modificados con nanotubos de difenilalanina, glutaraldehído como agente entrecruzante y peroxidasa de palma real como agente de reconocimiento biológico para la detección de peróxido de hidrógeno. Este proyecto consistió de cuatro etapas, la primera fue la extracción y semipurificación de la peroxidasa proveniente de las hojas de palma real. La enzima se obtuvo con un grado de purificación de 6,5 y una actividad específica final de 504 U/mg. Seguidamente se modificaron por adsorción física los electrodos con una solución que contenía nanotubos de péptidos, glutaraldehído y peroxidasa de palma real. La reducción bioelectrocatalítica del peróxido de hidrógeno se observó a un potencial redox de -0.4 V vs Ag. Este proceso fue controlado en la superficie del electrodo por los procesos de difusión en un rango de velocidad de barrido lineal de 50- 500 mV/s. Posteriormente se estudió la influencia del pH hacia la respuesta del biosensor, dando un rango de trabajo entre 5-10 El rango lineal exhibido del biosensor fue 500- M para la detección de peróxido de hidrógeno, Estos parámetros analíticos se dedujeron de analizar los resultados que se obtuvieron al utilizar cronoamperometría.
publishDate 2016
dc.date.available.none.fl_str_mv 2016
2024-03-03T22:43:27Z
dc.date.created.none.fl_str_mv 2016
dc.date.issued.none.fl_str_mv 2016
dc.date.accessioned.none.fl_str_mv 2024-03-03T22:43:27Z
dc.type.local.none.fl_str_mv Tesis/Trabajo de grado - Monografía - Pregrado
dc.type.hasversion.none.fl_str_mv http://purl.org/coar/resource_type/c_7a1f
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format http://purl.org/coar/version/c_b1a7d7d4d402bcce
dc.identifier.uri.none.fl_str_mv https://noesis.uis.edu.co/handle/20.500.14071/34941
dc.identifier.instname.none.fl_str_mv Universidad Industrial de Santander
dc.identifier.reponame.none.fl_str_mv Universidad Industrial de Santander
dc.identifier.repourl.none.fl_str_mv https://noesis.uis.edu.co
url https://noesis.uis.edu.co/handle/20.500.14071/34941
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identifier_str_mv Universidad Industrial de Santander
dc.language.iso.none.fl_str_mv spa
language spa
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dc.rights.creativecommons.none.fl_str_mv Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
rights_invalid_str_mv Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
http://creativecommons.org/licenses/by/4.0/
http://creativecommons.org/licenses/by-nc/4.0
Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidad Industrial de Santander
dc.publisher.faculty.none.fl_str_mv Facultad de Ciencias
dc.publisher.program.none.fl_str_mv Química
dc.publisher.school.none.fl_str_mv Escuela de Química
publisher.none.fl_str_mv Universidad Industrial de Santander
institution Universidad Industrial de Santander
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spelling Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)http://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by-nc/4.0Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)http://purl.org/coar/access_right/c_abf2Castillo León, John JairoVargas Ramirez, Jesus Alberto2024-03-03T22:43:27Z20162024-03-03T22:43:27Z20162016https://noesis.uis.edu.co/handle/20.500.14071/34941Universidad Industrial de SantanderUniversidad Industrial de Santanderhttps://noesis.uis.edu.coEn este trabajo de grado se desarrolló un biosensor amperométrico utilizando electrodos serigrafiados de oro que fueron modificados con nanotubos de difenilalanina, glutaraldehído como agente entrecruzante y peroxidasa de palma real como agente de reconocimiento biológico para la detección de peróxido de hidrógeno. Este proyecto consistió de cuatro etapas, la primera fue la extracción y semipurificación de la peroxidasa proveniente de las hojas de palma real. La enzima se obtuvo con un grado de purificación de 6,5 y una actividad específica final de 504 U/mg. Seguidamente se modificaron por adsorción física los electrodos con una solución que contenía nanotubos de péptidos, glutaraldehído y peroxidasa de palma real. La reducción bioelectrocatalítica del peróxido de hidrógeno se observó a un potencial redox de -0.4 V vs Ag. Este proceso fue controlado en la superficie del electrodo por los procesos de difusión en un rango de velocidad de barrido lineal de 50- 500 mV/s. Posteriormente se estudió la influencia del pH hacia la respuesta del biosensor, dando un rango de trabajo entre 5-10 El rango lineal exhibido del biosensor fue 500- M para la detección de peróxido de hidrógeno, Estos parámetros analíticos se dedujeron de analizar los resultados que se obtuvieron al utilizar cronoamperometría.PregradoQuímicoDevelopment of an amperometric biosensor for hydrogen peroxide by using peptide nanotubes and royal palm peroxidase (roystonea regia) on gold screen printed electrode :application/pdfspaUniversidad Industrial de SantanderFacultad de CienciasQuímicaEscuela de QuímicaBiosensorPeroxidasa De Palma RealElectrodo De OroNanotubos De Péptidos.In this work we developed a novel amperometric hydrogen peroxide biosensor based on the interaction of royal palm peroxidase (Roystonea regia) and peptide nanotubes by using glutaraldehyde as a linker on gold screen printed electrode. The development of the enzyme electrode consisted in four steps. The first step was the extraction and semi-purification of the peroxidase from royal palm tree. This process allowed to increase the specific activity and purification factor to 504.34 U / mg and 6.5 respectively. Then the electrode surface was modified with royal palm peroxidase by using peptide nanotube and glutaraldehydewhich allowed the electronic communication between the enzyme and the electrode surface. This step allowed the adsorption of peroxidase on the electrode surface. Bioelectrocatalytic reduction of hydrogen peroxide is observed at a redox potential -0.4 V vs Ag. This fact was demonstrated by the increasing on the electrocatalytic current of reduction at different concentrations of hydrogen peroxide. It was found that the electron transfer process was controlled superficially and depended on the pH of the solution. Based on the results from cronoamperometrythe enzyme electrode showed a linear response to hydrogen peroxide over a concentration range from 500 µM to 6000 µM with a detection limit of 432.71 µM and a sensibility of 0.024.Desarrollo de un biosensor amperométrico para la detección de peróxido de hidrogeno utilizando electrodos serigrafiados de oro modificados con peroxidasa de palma real (roystonea regia) y nanotubos de péptidosBiosensor, Royal Palm Peroxidase, Gold Screen Printed Electrode, Peptide Nanotubes.Tesis/Trabajo de grado - Monografía - Pregradohttp://purl.org/coar/resource_type/c_7a1fhttp://purl.org/coar/version/c_b1a7d7d4d402bcceORIGINALCarta de autorización.pdfapplication/pdf338500https://noesis.uis.edu.co/bitstreams/8f341879-9a4c-45f3-8165-89be70df5fef/download4a698e6e6915979cd219f43a3e56f978MD51Documento.pdfapplication/pdf2910686https://noesis.uis.edu.co/bitstreams/5a9cd407-ac56-4647-bb82-ad1237bbd6a2/download4b00766038b6d3e3816f2577121976a7MD52Nota de proyecto.pdfapplication/pdf148727https://noesis.uis.edu.co/bitstreams/a760ebd0-8f72-4e3b-88e5-47e85b3957af/download6c3b7a975ab33b897f130b6fea0f2f14MD5320.500.14071/34941oai:noesis.uis.edu.co:20.500.14071/349412024-03-03 17:43:27.557http://creativecommons.org/licenses/by-nc/4.0http://creativecommons.org/licenses/by/4.0/open.accesshttps://noesis.uis.edu.coDSpace at UISnoesis@uis.edu.co