Biocompatible Graphene Oxide Nanosheets Densely Functionalized with Biologically Active Molecules for Biosensing Applications

Journal Article (2021)
Author(s)

Benjamin A.E. Lehner (TU Delft - BN/Stan Brouns Lab, Kavli institute of nanoscience Delft)

Dominik Benz (TU Delft - ChemE/Chemical Engineering, TU Delft - ChemE/Product and Process Engineering)

Stanislav A. Moshkalev (University of Campinas)

Anne S. Meyer (University of Rochester)

Monica A. Cotta (University of Campinas)

Richard Janissen (BN/Cees Dekker Lab, Kavli institute of nanoscience Delft)

Research Group
ChemE/Product and Process Engineering
DOI related publication
https://doi.org/10.1021/acsanm.1c01522
More Info
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Publication Year
2021
Language
English
Research Group
ChemE/Product and Process Engineering
Issue number
8
Volume number
4
Pages (from-to)
8334-8342
Downloads counter
310
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Institutional Repository
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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.