Publicação
Hydrogel-forming ability and biological characterization of exopolysaccharide (EPS) from porphyridium cruentum
| dc.contributor.author | Duarte, Marta M. | |
| dc.contributor.author | Suprinovych, Artem | |
| dc.contributor.author | Veiga, Anabela | |
| dc.contributor.author | Lopes, Ana I. | |
| dc.contributor.author | Tavaria, Freni K. | |
| dc.contributor.author | Morais, Rui C. | |
| dc.contributor.author | Oliveira, Ana L. | |
| dc.date.accessioned | 2026-05-18T16:12:26Z | |
| dc.date.available | 2026-05-18T16:12:26Z | |
| dc.date.issued | 2026-05-01 | |
| dc.description.abstract | Exopolysaccharides (EPSs) are emerging as sustainable polymers for biomedical hydrogels. Here, we report hydrogels from sulfated EPSs produced by Porphyridium cruentum and ionically crosslinked with Ca2+, Ce3+, or Cu2+ to generate tunable networks with bioactive potential. Rheological analysis showed viscoelastic behavior was primarily governed by cation nature and accessible binding site density, with diminishing gains above 2.5 wt% EPS and limited benefit beyond 10 wt% crosslinker. Ce3+ produced the most solid-like gel, Ca2+ yielded more thixotropic networks, and Cu2+ promoted rapid, heterogeneous crosslinking consistent with fast surface complexation. These network signatures showed distinct in vitro performances. Cation selection tuned antibacterial activity against Staphylococcus aureus and Escherichia coli, with Cu2+ achieving rapid bactericidal effects and Ce3+ enabling an 8-log reduction after 24 h. The ABTS assay showed that Ca2+- and Ce3+-crosslinked gels had antioxidant potential (≥40 µM Trolox eq.mg−1); however, antioxidant capacity was assay dependent. Conditioned-medium assays showed ≥75% viability at day 3 for Ca2+- and Ce3+-crosslinked gels against human dermal fibroblasts (HDFs), while only Ce3+-crosslinked gels were cytocompatible against human keratinocytes (HaCaTs). Cu2+-crosslinked gels were highly cytotoxic across all tested conditions. Macrophage cytokine readouts (TNF-α and IL-6) indicated formulation-dependent immunobiological response. This work establishes microalgal EPSs as versatile polymers and links crosslinking chemistry to rheological modulation and multifunctional biomedical performance, while direct wound-healing efficacy remains to be demonstrated in future in vivo or wound repair functional models. | eng |
| dc.identifier.doi | 10.3390/gels12050352 | |
| dc.identifier.eid | 105040194405 | |
| dc.identifier.other | c3485541-261e-4fc2-9343-a61f4785d439 | |
| dc.identifier.pmid | 42196038 | |
| dc.identifier.uri | http://hdl.handle.net/10400.14/57743 | |
| dc.identifier.wos | 001774612800001 | |
| dc.language.iso | eng | |
| dc.peerreviewed | yes | |
| dc.publisher | MDPI | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject | EPS | eng |
| dc.subject | Porphyridium cruentum | eng |
| dc.subject | Hydrogel | eng |
| dc.subject | Ionic crosslinking | eng |
| dc.subject | Antioxidant | eng |
| dc.subject | Antimicrobial | eng |
| dc.subject | Immunomodulatory | eng |
| dc.title | Hydrogel-forming ability and biological characterization of exopolysaccharide (EPS) from porphyridium cruentum | |
| dc.type | research article | |
| dspace.entity.type | Publication | |
| oaire.citation.issue | 5 | |
| oaire.citation.volume | 12 | |
| oaire.version | http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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