Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno
La construcción de nuevos dispositivos de detección es una de las tendencias más marcadas en cuanto a química analítica moderna se refiere. El objetivo de este trabajo de grado fue la modificación de electrodos serigrafiados de grafeno con peroxidasa de pasto guinea (Panicum maximum) para la detecci...
- Autores:
-
Solano Contreras, Xuxan Hasbleidy Del Rocio
- 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:20.500.14071/34972
- Palabra clave:
- Pasto Guinea
Peroxidasa
Biosensor
Grafeno.
The main objective of this work was the modification of Graphene screen-printed electrodes with peroxidase of guinea grass (Panicum maximum) for the enzymatic detection of hydrogen peroxide. This work was development in three stages; first the enzyme was extracted and partially purified. The enzyme was obtained with a purification degree of 1
19
a specific activity of 724.7 U/mg with a yield of 24.3%. The second stage involved the immobilization of the enzyme over graphite screen-printed electrodes. And finally
the modified electrode was characterized through electrochemical techniques such as cyclic voltammetry
chronoamperometry and spectroscopy impedance. The bioelectrocatalytic reduction of hydrogen peroxidase was estimated to a redox potential of 1-10 V Ag/AgCl/KCl(sat). This process was diffusionally controlled over the surface of the electrode. Subsequently the biosensor response was studied under the influence of pH
obtaining a wide range of work since pH 5 until pH 10 and optimum work pH of 8.0. The displayed linear range was 100- results of chronoamperometry studies and calibration curves and This results were presented at the II Colombian Congress of Electrochemistry and 2nd Symposium on Nanoscience and Nanotechnology in poster mode.
- Rights
- License
- Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
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dc.title.none.fl_str_mv |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
dc.title.english.none.fl_str_mv |
Peroxidase, Biosensor, Graphene Oxide. |
title |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
spellingShingle |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno Pasto Guinea Peroxidasa Biosensor Grafeno. The main objective of this work was the modification of Graphene screen-printed electrodes with peroxidase of guinea grass (Panicum maximum) for the enzymatic detection of hydrogen peroxide. This work was development in three stages; first the enzyme was extracted and partially purified. The enzyme was obtained with a purification degree of 1 19 a specific activity of 724.7 U/mg with a yield of 24.3%. The second stage involved the immobilization of the enzyme over graphite screen-printed electrodes. And finally the modified electrode was characterized through electrochemical techniques such as cyclic voltammetry chronoamperometry and spectroscopy impedance. The bioelectrocatalytic reduction of hydrogen peroxidase was estimated to a redox potential of 1-10 V Ag/AgCl/KCl(sat). This process was diffusionally controlled over the surface of the electrode. Subsequently the biosensor response was studied under the influence of pH obtaining a wide range of work since pH 5 until pH 10 and optimum work pH of 8.0. The displayed linear range was 100- results of chronoamperometry studies and calibration curves and This results were presented at the II Colombian Congress of Electrochemistry and 2nd Symposium on Nanoscience and Nanotechnology in poster mode. |
title_short |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
title_full |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
title_fullStr |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
title_full_unstemmed |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
title_sort |
Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogeno |
dc.creator.fl_str_mv |
Solano Contreras, Xuxan Hasbleidy Del Rocio |
dc.contributor.advisor.none.fl_str_mv |
Castillo León, John Jairo |
dc.contributor.author.none.fl_str_mv |
Solano Contreras, Xuxan Hasbleidy Del Rocio |
dc.subject.none.fl_str_mv |
Pasto Guinea Peroxidasa Biosensor Grafeno. |
topic |
Pasto Guinea Peroxidasa Biosensor Grafeno. The main objective of this work was the modification of Graphene screen-printed electrodes with peroxidase of guinea grass (Panicum maximum) for the enzymatic detection of hydrogen peroxide. This work was development in three stages; first the enzyme was extracted and partially purified. The enzyme was obtained with a purification degree of 1 19 a specific activity of 724.7 U/mg with a yield of 24.3%. The second stage involved the immobilization of the enzyme over graphite screen-printed electrodes. And finally the modified electrode was characterized through electrochemical techniques such as cyclic voltammetry chronoamperometry and spectroscopy impedance. The bioelectrocatalytic reduction of hydrogen peroxidase was estimated to a redox potential of 1-10 V Ag/AgCl/KCl(sat). This process was diffusionally controlled over the surface of the electrode. Subsequently the biosensor response was studied under the influence of pH obtaining a wide range of work since pH 5 until pH 10 and optimum work pH of 8.0. The displayed linear range was 100- results of chronoamperometry studies and calibration curves and This results were presented at the II Colombian Congress of Electrochemistry and 2nd Symposium on Nanoscience and Nanotechnology in poster mode. |
dc.subject.keyword.none.fl_str_mv |
The main objective of this work was the modification of Graphene screen-printed electrodes with peroxidase of guinea grass (Panicum maximum) for the enzymatic detection of hydrogen peroxide. This work was development in three stages; first the enzyme was extracted and partially purified. The enzyme was obtained with a purification degree of 1 19 a specific activity of 724.7 U/mg with a yield of 24.3%. The second stage involved the immobilization of the enzyme over graphite screen-printed electrodes. And finally the modified electrode was characterized through electrochemical techniques such as cyclic voltammetry chronoamperometry and spectroscopy impedance. The bioelectrocatalytic reduction of hydrogen peroxidase was estimated to a redox potential of 1-10 V Ag/AgCl/KCl(sat). This process was diffusionally controlled over the surface of the electrode. Subsequently the biosensor response was studied under the influence of pH obtaining a wide range of work since pH 5 until pH 10 and optimum work pH of 8.0. The displayed linear range was 100- results of chronoamperometry studies and calibration curves and This results were presented at the II Colombian Congress of Electrochemistry and 2nd Symposium on Nanoscience and Nanotechnology in poster mode. |
description |
La construcción de nuevos dispositivos de detección es una de las tendencias más marcadas en cuanto a química analítica moderna se refiere. El objetivo de este trabajo de grado fue la modificación de electrodos serigrafiados de grafeno con peroxidasa de pasto guinea (Panicum maximum) para la detección enzimática de peróxido de hidrógeno (H2O2). Para tal fin, el trabajo se desarrolló en tres etapas, la primera etapa consistió en la extracción y purificación parcial de la enzima, la enzima se obtuvo con una actividad específica de 724,7 U/mg. La segunda etapa consistió en la inmovilización por adsorción física del extracto enzimático sobre electrodos serigrafiados de grafeno y finalmente la etapa de caracterización mediante técnicas electroquímicas tales como voltamperometría, cronoamperometría y espectroscopia de impedancia electroquímica. La reducción bioelectrocatalítica del peróxido de hidrógeno se observó a un potencial de -1,0 V vs Ag/AgCl/KCl(sat). Este fue un proceso controlado en la superficie del electrodo en un rango de velocidad de barrido lineal de 50- 600 mVs-1. Posteriormente se estudió la dependencia de la respuesta del electrodo modificado SPE/PPG frente a diferentes valores de pH, obteniéndose un pH óptimo de 8.0. El rango lineal exhibido fue 100- 35100 analíticos se dedujeron de los resultados obtenidos en cronoamperometría. Parte de estos resultados fueron presentados en el II Congreso Colombiano de Electroquímica y 2° Simposio en Nanociencia y Nanotecnología en modalidad poster. |
publishDate |
2016 |
dc.date.available.none.fl_str_mv |
2016 2024-03-03T22:43:32Z |
dc.date.created.none.fl_str_mv |
2016 |
dc.date.issued.none.fl_str_mv |
2016 |
dc.date.accessioned.none.fl_str_mv |
2024-03-03T22:43:32Z |
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 |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/version/c_b1a7d7d4d402bcce |
format |
http://purl.org/coar/version/c_b1a7d7d4d402bcce |
dc.identifier.uri.none.fl_str_mv |
https://noesis.uis.edu.co/handle/20.500.14071/34972 |
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/20.500.14071/34972 https://noesis.uis.edu.co |
identifier_str_mv |
Universidad Industrial de Santander |
dc.language.iso.none.fl_str_mv |
spa |
language |
spa |
dc.rights.none.fl_str_mv |
http://creativecommons.org/licenses/by/4.0/ |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.license.none.fl_str_mv |
Attribution-NonCommercial 4.0 International (CC BY-NC 4.0) |
dc.rights.uri.none.fl_str_mv |
http://creativecommons.org/licenses/by-nc/4.0 |
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 JairoSolano Contreras, Xuxan Hasbleidy Del Rocio2024-03-03T22:43:32Z20162024-03-03T22:43:32Z20162016https://noesis.uis.edu.co/handle/20.500.14071/34972Universidad Industrial de SantanderUniversidad Industrial de Santanderhttps://noesis.uis.edu.coLa construcción de nuevos dispositivos de detección es una de las tendencias más marcadas en cuanto a química analítica moderna se refiere. El objetivo de este trabajo de grado fue la modificación de electrodos serigrafiados de grafeno con peroxidasa de pasto guinea (Panicum maximum) para la detección enzimática de peróxido de hidrógeno (H2O2). Para tal fin, el trabajo se desarrolló en tres etapas, la primera etapa consistió en la extracción y purificación parcial de la enzima, la enzima se obtuvo con una actividad específica de 724,7 U/mg. La segunda etapa consistió en la inmovilización por adsorción física del extracto enzimático sobre electrodos serigrafiados de grafeno y finalmente la etapa de caracterización mediante técnicas electroquímicas tales como voltamperometría, cronoamperometría y espectroscopia de impedancia electroquímica. La reducción bioelectrocatalítica del peróxido de hidrógeno se observó a un potencial de -1,0 V vs Ag/AgCl/KCl(sat). Este fue un proceso controlado en la superficie del electrodo en un rango de velocidad de barrido lineal de 50- 600 mVs-1. Posteriormente se estudió la dependencia de la respuesta del electrodo modificado SPE/PPG frente a diferentes valores de pH, obteniéndose un pH óptimo de 8.0. El rango lineal exhibido fue 100- 35100 analíticos se dedujeron de los resultados obtenidos en cronoamperometría. Parte de estos resultados fueron presentados en el II Congreso Colombiano de Electroquímica y 2° Simposio en Nanociencia y Nanotecnología en modalidad poster.PregradoQuímicoScreen printed electrodes modified with peroxidase from grass guinea (panicum maximum) for enzymatic detection of hydrogen peroxide.application/pdfspaUniversidad Industrial de SantanderFacultad de CienciasQuímicaEscuela de QuímicaPasto GuineaPeroxidasaBiosensorGrafeno.The main objective of this work was the modification of Graphene screen-printed electrodes with peroxidase of guinea grass (Panicum maximum) for the enzymatic detection of hydrogen peroxide. This work was development in three stages; first the enzyme was extracted and partially purified. The enzyme was obtained with a purification degree of 119a specific activity of 724.7 U/mg with a yield of 24.3%. The second stage involved the immobilization of the enzyme over graphite screen-printed electrodes. And finallythe modified electrode was characterized through electrochemical techniques such as cyclic voltammetrychronoamperometry and spectroscopy impedance. The bioelectrocatalytic reduction of hydrogen peroxidase was estimated to a redox potential of 1-10 V Ag/AgCl/KCl(sat). This process was diffusionally controlled over the surface of the electrode. Subsequently the biosensor response was studied under the influence of pHobtaining a wide range of work since pH 5 until pH 10 and optimum work pH of 8.0. The displayed linear range was 100- results of chronoamperometry studies and calibration curves and This results were presented at the II Colombian Congress of Electrochemistry and 2nd Symposium on Nanoscience and Nanotechnology in poster mode.Electrodos serigrafiados de grafeno modificados con peroxidasa de pasto guinea (panicum maximun) para la detección enzimática de peróxido de hidrogenoPeroxidase, Biosensor, Graphene Oxide.Tesis/Trabajo de grado - Monografía - Pregradohttp://purl.org/coar/resource_type/c_7a1fhttp://purl.org/coar/version/c_b1a7d7d4d402bcceORIGINALCarta de autorización.pdfapplication/pdf266349https://noesis.uis.edu.co/bitstreams/1182ad08-d6da-4419-8e93-6a6d9b215f7c/downloadd71f51ed7b2458355222fe85fa5d06abMD51Documento.pdfapplication/pdf2685993https://noesis.uis.edu.co/bitstreams/dbd96ed3-b46f-4656-b0bc-b9fd2fd3ea6f/download226fcbd7ded74f9cac97518f9069fbedMD52Nota de proyecto.pdfapplication/pdf162364https://noesis.uis.edu.co/bitstreams/274498ea-2733-4309-bc0e-be19c728adad/downloada186e3a2f9c051e8ffc9d8abc36bf7c6MD5320.500.14071/34972oai:noesis.uis.edu.co:20.500.14071/349722024-03-03 17:43:32.789http://creativecommons.org/licenses/by-nc/4.0http://creativecommons.org/licenses/by/4.0/open.accesshttps://noesis.uis.edu.coDSpace at UISnoesis@uis.edu.co |