Bioactive polymeric scaffolds: multivalent functionalization by Thermal Azide–Alkyne Cycloaddition with Alkynyl Dicarbamates
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ISSN: 1525-7797
E-ISSN: 1526-4602
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American Chemical Society
Abstract
Multivalency enables interactions with higher affinities and specificities than monovalent interactions. The strategy exploited by nature to modulate biorecognition has inspired the design of multivalent conjugates with therapeutic properties. However, chemical functionalization often requires coupling agents, additives, or metal catalysts that complicate isolation and purification. Herein, azide–alkyne cycloaddition (AAC) with alkynyl dicarbamates (Alk-R) is presented as a flexible, reliable, atom-economical, and user-friendly strategy for the multivalent functionalization of polymeric scaffolds. Alk-R functionalized with biologically relevant ligands have been prepared and used for the multivalent AAC functionalization of azide-bearing dendrimers and block copolymers. The resulting polymers with double multivalency reveal a platform for the development of bioinspired functional systems with promising applications in drug delivery: block copolymer micelles and multifunctional nanocarriers with synergistically integrated probes-ligands-drugs. The extension of this strategy to other ligands and scaffolds is expected to open up a wide range of therapeutic and diagnostic opportunities.
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Tawara, M. H., Correa, J., Leire, E., Gonzalez, B. D., Parcero-Bouzas, S., Liko, F., & Fernandez-Megia, E. (2025). Bioactive Polymeric Scaffolds: Multivalent Functionalization by Thermal Azide–Alkyne Cycloaddition with Alkynyl Dicarbamates. "Biomacromolecules". https://doi.org/10.1021/acs.biomac.5c00038
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https://doi.org/10.1021/acs.biomac.5c00038Sponsors
This work was supported by grant PID2021-127684OB-I00 funded by MCIN/AEI/10.13039/501100011033 and by ERDF “A way of making Europe.” The authors thank the f inancial support from Xunta de Galicia (ED431C 2022/21, and Centro de Investigación do Sistema Universitario de Galicia accreditation 2023-2027, ED431G 2023/03) and the European Union (European Regional Development Fund� ERDF). B.D.G. thanks Xunta de Galicia for a predoctoral grant. E.L. and F.L. thank the European Commission, Education, Audiovisual and Cultural Executive Agency (EACEA) for an Erasmus Mundus grant under the NanoFar Joint Doctoral Program
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Copyright © 2025 American Chemical Society
Attribution 4.0 International
Attribution 4.0 International







