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Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents
Squaric acid (SA) is a compound with potential to crosslink biomacromolecules. Although SA has become over the last years a well-known crosslinking agent as a result of its good biocompatibility, glutaraldehyde (GA), a compound with proven cytotoxicity is still one of the most used crosslinkers to d...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318457/ https://www.ncbi.nlm.nih.gov/pubmed/35889669 http://dx.doi.org/10.3390/nano12142445 |
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author | Rusu, Alina Gabriela Chiriac, Aurica P. Nita, Loredana Elena Balan, Vera Serban, Alexandru Mihail Croitoriu, Alexandra |
author_facet | Rusu, Alina Gabriela Chiriac, Aurica P. Nita, Loredana Elena Balan, Vera Serban, Alexandru Mihail Croitoriu, Alexandra |
author_sort | Rusu, Alina Gabriela |
collection | PubMed |
description | Squaric acid (SA) is a compound with potential to crosslink biomacromolecules. Although SA has become over the last years a well-known crosslinking agent as a result of its good biocompatibility, glutaraldehyde (GA), a compound with proven cytotoxicity is still one of the most used crosslinkers to develop nanomaterials. In this regard, the novelty of the present study consists in determining whether it may be possible to substitute GA with a new bifunctional and biocompatible compound, such as SA, in the process of enzyme immobilization on the surface of magnetic nanoparticles (MNPs). Thus, a direct comparison between SA- and GA-functionalized magnetic nanoparticles was realized in terms of physico-chemical properties and ability to immobilize catalytic enzymes. The optimal conditions of the synthesis of the two types of GOx-immobilized MNPs were described, thus emphasizing the difference between the two reagents. Scanning Electron Microscopy and Dynamic Light Scattering were used for size, shape and colloidal stability characterization of the pristine MNPs and of those coupled with GOx. Binding of GOx to MNPs by using GA or SA was confirmed by FT-IR spectroscopy. The stability of the immobilized and free enzyme was investigated by measuring the enzymatic activity. The study confirmed that the resulting activity of the immobilized enzyme and the optimization of enzyme immobilization depended on the type of reagent used and duration of the process. The catalytic performance of immobilized enzyme was tested, revealing that the long-term colloidal stability of SA-functionalized MNPs was superior to those prepared with GA. In conclusion, the SA-functionalized bioconjugates have a better potential as compared to the GA-modified nanosystems to be regarded as catalytic nanodevices for biomedical purposes such as biosensors. |
format | Online Article Text |
id | pubmed-9318457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93184572022-07-27 Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents Rusu, Alina Gabriela Chiriac, Aurica P. Nita, Loredana Elena Balan, Vera Serban, Alexandru Mihail Croitoriu, Alexandra Nanomaterials (Basel) Article Squaric acid (SA) is a compound with potential to crosslink biomacromolecules. Although SA has become over the last years a well-known crosslinking agent as a result of its good biocompatibility, glutaraldehyde (GA), a compound with proven cytotoxicity is still one of the most used crosslinkers to develop nanomaterials. In this regard, the novelty of the present study consists in determining whether it may be possible to substitute GA with a new bifunctional and biocompatible compound, such as SA, in the process of enzyme immobilization on the surface of magnetic nanoparticles (MNPs). Thus, a direct comparison between SA- and GA-functionalized magnetic nanoparticles was realized in terms of physico-chemical properties and ability to immobilize catalytic enzymes. The optimal conditions of the synthesis of the two types of GOx-immobilized MNPs were described, thus emphasizing the difference between the two reagents. Scanning Electron Microscopy and Dynamic Light Scattering were used for size, shape and colloidal stability characterization of the pristine MNPs and of those coupled with GOx. Binding of GOx to MNPs by using GA or SA was confirmed by FT-IR spectroscopy. The stability of the immobilized and free enzyme was investigated by measuring the enzymatic activity. The study confirmed that the resulting activity of the immobilized enzyme and the optimization of enzyme immobilization depended on the type of reagent used and duration of the process. The catalytic performance of immobilized enzyme was tested, revealing that the long-term colloidal stability of SA-functionalized MNPs was superior to those prepared with GA. In conclusion, the SA-functionalized bioconjugates have a better potential as compared to the GA-modified nanosystems to be regarded as catalytic nanodevices for biomedical purposes such as biosensors. MDPI 2022-07-17 /pmc/articles/PMC9318457/ /pubmed/35889669 http://dx.doi.org/10.3390/nano12142445 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Rusu, Alina Gabriela Chiriac, Aurica P. Nita, Loredana Elena Balan, Vera Serban, Alexandru Mihail Croitoriu, Alexandra Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title | Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title_full | Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title_fullStr | Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title_full_unstemmed | Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title_short | Synthesis and Comparative Studies of Glucose Oxidase Immobilized on Fe(3)O(4) Magnetic Nanoparticles Using Different Coupling Agents |
title_sort | synthesis and comparative studies of glucose oxidase immobilized on fe(3)o(4) magnetic nanoparticles using different coupling agents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9318457/ https://www.ncbi.nlm.nih.gov/pubmed/35889669 http://dx.doi.org/10.3390/nano12142445 |
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