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Biocompatible Graphene Oxide Nanosheets Densely Functionalized with Biologically Active Molecules for Biosensing Applications.
Lehner, Benjamin A E; Benz, Dominik; Moshkalev, Stanislav A; Meyer, Anne S; Cotta, Monica A; Janissen, Richard.
Afiliação
  • Lehner BAE; Kavli Institute of Nanoscience, Delft University of Technology, Delft 2629HZ, The Netherlands.
  • Benz D; Chemical Engineering, Delft University of Technology, Delft 2629HZ, The Netherlands.
  • Moshkalev SA; Center of Semiconductor Components and Nanotechnologies, University of Campinas, Campinas, Sao Paulo 13083-870, Brazil.
  • Meyer AS; Department of Biology, University of Rochester, Rochester, New York 14627, United States.
  • Cotta MA; Laboratory of Nano and Biosystems, Department of Applied Physics, University of Campinas, Campinas, Sao Paulo 13083-859, Brazil.
  • Janissen R; Kavli Institute of Nanoscience, Delft University of Technology, Delft 2629HZ, The Netherlands.
ACS Appl Nano Mater ; 4(8): 8334-8342, 2021 Aug 27.
Article em En | MEDLINE | ID: mdl-34485844
ABSTRACT
Graphene oxide (GO) has immense potential for widespread use in diverse in vitro and in vivo biomedical applications owing to its thermal and chemical resistance, excellent electrical properties and solubility, and high surface-to-volume ratio. However, development of GO-based biological nanocomposites and biosensors has been hampered by its poor intrinsic biocompatibility and difficult covalent biofunctionalization across its lattice. Many studies exploit the strategy of chemically modifying GO by noncovalent and reversible attachment of (bio)molecules or sole covalent biofunctionalization of residual moieties at the lattice edges, resulting in a low coating coverage and a largely bioincompatible composite. Here, we address these problems and present a facile yet powerful method for the covalent biofunctionalization of GO using colamine (CA) and the poly(ethylene glycol) cross-linker that results in a vast improvement in the biomolecular coating density and heterogeneity across the entire GO lattice. We further demonstrate that our biofunctionalized GO with CA as the cross-linker provides superior nonspecific biomolecule adhesion suppression with increased biomarker detection sensitivity in a DNA-biosensing assay compared to the (3-aminopropyl)triethoxysilane cross-linker. Our optimized biofunctionalization method will aid the development of GO-based in situ applications including biosensors, tissue nanocomposites, and drug carriers.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article