Targeting B Lymphocytes Using Protein‐Functionalized Graphene Oxide
The high surface area and the possibility of surface functionalization associated with a high biocompatibility endow graphene oxide with a great potential for biomedical applications. Although this material has been widely investigated for cancer therapy, it has been scarcely used for the treatment...
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| Autores principales: | , , , , , |
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| Formato: | article |
| Lenguaje: | EN |
| Publicado: |
Wiley-VCH
2021
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| Materias: | |
| Acceso en línea: | https://doaj.org/article/e23b6be94bc94d988af9c5457e12e7de |
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| Sumario: | The high surface area and the possibility of surface functionalization associated with a high biocompatibility endow graphene oxide with a great potential for biomedical applications. Although this material has been widely investigated for cancer therapy, it has been scarcely used for the treatment of autoimmune diseases. Herein, graphene oxide–lysozyme stable conjugates are prepared by a straightforward noncovalent functionalization approach. The complexes are able to selectively target a B lymphocyte cell model, which expresses a lysozyme‐specific B cell receptor. The results suggest the use of graphene oxide as a promising nanocarrier for the targeted therapy of B‐cell‐mediated autoimmune diseases, allowing overcoming the severe inconveniences associated with available B‐cell‐targeted therapies. |
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