SURFACE “CLICK†REACTION BETWEEN ACETYLENE-DECORATED POLYMERIC PLATFORM AND AZIDE-DECORATED COMPOUNDS
Bidhari Pidhatika and
Melanie Macgregor ()
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Bidhari Pidhatika: Research Center for Polymer Technology, National Research and Innovation Agency (BRIN), Republic of Indonesia2Collaborative Research Center for Biomedical Scaffolds, National Research and Innovation Agency of the Republic of Indonesia and Universitas Gadjah Mada, Jalan Denta No. 1, Sekip Utara, Yogyakarta 55281, Indonesia
Melanie Macgregor: ��Flinders Institute for Nanoscale Science & Technology, College of Science and Engineering, Physical Sciences Building, Flinders University, Sturt Road, Bedford Park, South Australia 5042, Australia
Surface Review and Letters (SRL), 2023, vol. 30, issue 03, 1-12
Abstract:
A proof on concept study was conducted in the quest for dual-functional surfaces that provide both biopassivity and bioactivity. It presents the development of a biopassive platform that readily binds to bioactive molecules via copper-catalyzed acetylene-azide cycloaddition reaction. Acetylene-decorated poly(2-methyl-2-oxazoline) (PMOXA) brushes were grafted on an Nb2O5 surface. This biopassive brush platform was then exposed to various azide-decorated compounds of different sizes (molecular weight) and chemical structure, i.e. benzyl, mannose, and antimicrobial peptide (AMP), to react through the cycloaddition reaction. The different nature of the compounds “clicked†to the brushes requires different strategies of characterization. Time of flight-secondary ion mass spectroscopy (ToF-SIMS) results showed that benzyl-triazole-characteristic fragments were successfully bound to the surface. Fluorescence spectroscopy results indicated that mannose-azide molecules tagged with dye-carrying Concanavalin A (Con-A) could bind to the PMOXA-acetylene brush via specific and, to some extent, nonspecific interactions. Similarly, optical waveguide light-mode spectroscopy (OWLS) and quartz crystal microbalance-dissipation (QCM-D) analysis showed a successful reaction between AMP-azide and the PMOXA-acetylene brush platform. Together, these results validated the original approach of generating dual-functional surfaces using a “click†reaction between oxazoline brushes and a variety of ligands relevant to a range of applications.
Keywords: Acetylene; brush; “click†reaction; PMOXA; surface (search for similar items in EconPapers)
Date: 2023
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DOI: 10.1142/S0218625X23500166
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