Biocompatible Graphene Oxide Nanosheets Densely Functionalized with Biologically Active Molecules for Biosensing Applications
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 nanocomposi...
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Veröffentlicht in: | ACS applied nano materials 2021-08, Vol.4 (8), p.8334-8342 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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. |
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ISSN: | 2574-0970 2574-0970 |
DOI: | 10.1021/acsanm.1c01522 |