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Bioconjugation of carbon nanotubes (CNTs) with biomolecules promises exciting applications such as biosensing, nanobiocomposite formulation, design of drug vector systems, and probing protein interactions. Pristine CNTs, however, are virtually water-insoluble and difficult to evenly disperse in a liquid matrix. Therefore, it is necessary to attach molecules or functional groups to their sidewalls to enable bioconjugation. Both noncovalent and covalent procedures can be used to conjugate CNTs with a target biomolecule for a specific bioapplication. This chapter presents a few selected protocols that can be performed at any wet chemistry laboratory to purify and biofunctionalize CNTs. The preparation of CNTs modified with metallic nanoparticles, especially gold, is also described since biomolecules can bind and self-organize on the surfaces of such metal-decorated CNTs.
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http://dx.doi.org/10.1007/978-1-61779-151-2_32 | DOI Listing |
Nanomaterials (Basel)
August 2025
Department of Toxicology and Food Science, Faculty of Pharmacy, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland.
Overexpression of αvβ3 integrin is found in a diverse group of tumors originating from glial cells in the brain, making this transmembrane receptor a promising biomarker for molecular MRI diagnosis. In the study, we conjugated a monoclonal antibody against the β3 subunit (CD61) of the αvβ3 integrin receptor with carbon-encapsulated iron nanoparticles to yield Fe@C-(CH)-CONH-anti-CD61 bioconjugates that were used in dynamic susceptibility contrast magnetic resonance imaging (DSC-MRI). Wistar rats bearing C6 gliomas were injected as a single bolus (0.
View Article and Find Full Text PDFLangmuir
August 2025
Biomedical Engineering Center, Toyo University, 48-1 Oka, Asaka, Saitama 351-8510, Japan.
In label-free biosensors based on graphene, achieving both the specific recognition of target analytes and the suppression of the nonspecific adsorption of interfering substances remains a critical challenge. In this study, a linker molecule possessing a pyrene moiety capable of forming π-π stacking interactions and an active ester group suitable for bioconjugation was employed to construct a selective layer on graphene. Subsequently, a DNA aptamer as the receptor and a phospholipid-mimetic zwitterionic molecule for suppressing nonspecific adsorption were sequentially conjugated to the active ester groups.
View Article and Find Full Text PDFNat Commun
July 2025
Organic Synthesis Group, Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University, Ghent, Belgium.
Thiols are used in many click reactions, and are also excellent platforms for biomolecular click or bioconjugation reactions. The direct cross-coupling of two thiols is an attractive biomimetic concept for click chemistry, but leads to statistical mixtures of homo- and heterodimers. Here, we introduce a novel class of thiol-click reagents, bromo-ynones, where the kinetic differentiation between the first and second thiol addition onto these reagents facilitates a stepwise one-pot cross-clicking of two distinct thiols in aqueous media, without the need for intermediate isolation or purification.
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.
Carbon monoxide (CO) has demonstrated therapeutic benefits in reactive oxygen species (ROS)-rich environments, such as inflammation and cancer. However, the targeted delivery of CO remains challenging, limiting its clinical application and necessitating the development of improved CO-prodrugs. Herein, we report a radical-activated, metal-free, CO-prodrug designed to address delivery limitations and avoid metal-associated toxicity.
View Article and Find Full Text PDFLangmuir
July 2025
LSRE-LCM - Laboratory of Separation and Reaction Engineering - Laboratory of Catalysis and Materials, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, Porto 4200-465, Portugal.
This study demonstrates the successful immobilization of the enzyme glucose oxidase (GOx) onto 2D thermally exfoliated graphitic carbon nitride (GCN-T) via physical adsorption, producing a stable, reusable, and highly active bioconjugate. Binding was confirmed by scanning transmission electron microscopy (STEM) coupled with energy-dispersive spectroscopy (EDS), thermogravimetric analyses (TGAs), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). At the optimal conditions, GCN-T/GOx showed an immobilization yield of 88% and an activity of 0.
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