Myrcene-based tailored co-polymers as active pharmaceutical excipients : bio-based solutions for mucoadhesive excipients
Gintsburg, David and Sari, Selin Görkem and Molnar, Lana and Knoll, Annabelle and Kosti, Effrosyni‐Maria and Seybold, Anna and Deveci, Gozde and Bruns, Nico and Bernkop‐Schnürch, Andreas and Kali, Gergely (2026) Myrcene-based tailored co-polymers as active pharmaceutical excipients : bio-based solutions for mucoadhesive excipients. Advanced Functional Materials, 36 (60). e76618. ISSN 1616-3028 (https://doi.org/10.1002/adfm.76618)
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Abstract
Mucoadhesive polymers are widely used in drug delivery to prolong residence time on mucus-covered surfaces and enhance drug bioavailability, but conventional systems often suffer from broad molecular weight distributions and inconsistent performance. Here, three different amphiphilic co-polymers based on bio-sourced myrcene and PEG-methacrylate are synthesized via Reversible Addition–Fragmentation Chain Transfer polymerization, yielding well-defined polymers with narrow molar mass distributions. Structural analyses using 1H NMR spectroscopy and gel permeation chromatography confirm predominant 1,4-addition and low dispersity. Energy-filtered transmission electron microscopy and dynamic light scattering show self-assembled nanostructures with mean diameters below 60 nm. In vivo toxicity evaluation in Galleria mellonella larvae demonstrates 100% survival after 48 h and prolonged polymer residence compared with PEG_4000. Mucoadhesion and mucopermeation assays reveal enhanced adhesion with intestinal mucus, with up to 50% retention after 3 h, a 6.6-fold increase in mucus viscosity, and limited permeation (∼20%) into the mucus gel. Additionally, the polymers exhibit pronounced antioxidant activity (EC50 = 0.05% (m/V)) and antimicrobial activity against Escherichia coli (E. coli). Overall, high regioselectivity and controllable polymerization, combined with strong interactions with the intestinal mucosa, low toxicity, and biological effects, indicate that myrcene-based co-polymers are promising bio-sourced candidates for use as active excipients in drug delivery.
ORCID iDs
Gintsburg, David, Sari, Selin Görkem, Molnar, Lana, Knoll, Annabelle, Kosti, Effrosyni‐Maria, Seybold, Anna, Deveci, Gozde, Bruns, Nico
ORCID: https://orcid.org/0000-0001-6199-9995, Bernkop‐Schnürch, Andreas and Kali, Gergely;
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Item type: Article ID code: 96738 Dates: DateEvent27 July 2026Published6 July 2026Published Online5 June 2026AcceptedSubjects: Science > Chemistry Department: Faculty of Science > Pure and Applied Chemistry Depositing user: Pure Administrator Date deposited: 09 Jul 2026 07:10 Last modified: 09 Sep 2026 00:46 URI: https://strathprints.strath.ac.uk/id/eprint/96738
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