Lignin-based nanoparticles as both structural and active elements in self-assembling and self-healing multifunctional hydrogels for chronic wound management
| dc.contributor.author | Morena Gatius, Ángela Gala |
| dc.contributor.author | Pérez Rafael, Silvia |
| dc.contributor.author | Tzanov, Tzanko |
| dc.contributor.group | Universitat Politècnica de Catalunya. GBMI - Grup de Biotecnologia Molecular i Industrial |
| dc.contributor.other | Universitat Politècnica de Catalunya. Doctorat en Polímers i Biopolímers |
| dc.contributor.other | Universitat Politècnica de Catalunya. Departament d'Enginyeria Química |
| dc.date.accessioned | 2023-02-20T14:14:31Z |
| dc.date.available | 2023-02-20T14:14:31Z |
| dc.date.issued | 2022-11-30 |
| dc.description.abstract | Efficient wound healing is feasible when the dressing materials simultaneously target multiple factors causing wound chronicity, such as deleterious proteolytic and oxidative enzymes and bacterial infection. Herein, entirely bio-based multifunctional self-assembled hydrogels for wound healing were developed by simply mixing two biopolymers, thiolated hyaluronic acid (HA-SH) and silk fibroin (SF), with lignin-based nanoparticles (NPs) as both structural and functional elements. Sono-enzymatic lignin modification with natural phenolic compounds results in antibacterial and antioxidant phenolated lignin nanoparticles (PLN) capable of establishing multiple interactions with both polymers. These strong and dynamic polymer-NP interactions endow the hydrogels with self-healing and shear-thinning properties, and pH-responsive NP release is triggered at neutral to alkaline pH (7–9). Despite being a physically crosslinked hydrogel, the material was stable for at least 7 days, and its mechanical and functional properties can be tuned depending on the polymer and NP concentration. Furthermore, human skin cells in contact with the nanocomposite hydrogels for 7 days showed more than 93% viability, while the viability of clinically relevant Staphylococcus aureus and Pseudomonas aeruginosa was reduced by 99.7 and 99.0%, respectively. The hydrogels inhibited up to 52% of the activity of myeloperoxidase and matrix metalloproteinases, responsible for wound chronicity, and showed a strong antioxidant effect, which are crucial features promoting wound healing. |
| dc.description.peerreviewed | Peer Reviewed |
| dc.description.version | Postprint (published version) |
| dc.format.extent | 20 p. |
| dc.identifier.citation | Morena, A.G.; Perez, S.; Tzanov, T. Lignin-based nanoparticles as both structural and active elements in self-assembling and self-healing multifunctional hydrogels for chronic wound management. "Pharmaceutics (Basel)", 30 Novembre 2022, vol. 14, núm. 12, article 2658, p. 1-20. |
| dc.identifier.doi | 10.3390/pharmaceutics14122658 |
| dc.identifier.issn | 19994923 |
| dc.identifier.uri | https://hdl.handle.net/2117/383734 |
| dc.language.iso | eng |
| dc.publisher | Multidisciplinary Digital Publishing Institute (MDPI) |
| dc.relation.publisherversion | https://www.mdpi.com/1999-4923/14/12/2658 |
| dc.rights.access | Open Access |
| dc.rights.licensename | Attribution 4.0 International |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
| dc.subject | Àrees temàtiques de la UPC::Enginyeria química |
| dc.subject.lcsh | Regenerative medicine |
| dc.subject.lcsh | Biomedical materials |
| dc.subject.lemac | Medicina regenerativa |
| dc.subject.lemac | Materials biomèdics |
| dc.subject.other | Lignin nanoparticle |
| dc.subject.other | Hyaluronic acid |
| dc.subject.other | Silk fibroin |
| dc.subject.other | Self-assembling hydrogels |
| dc.subject.other | Chronic wounds |
| dc.subject.other | Antibacterial |
| dc.subject.other | Antioxidant |
| dc.subject.other | Wound enzymes inhibition |
| dc.subject.other | PH-responsiveness |
| dc.title | Lignin-based nanoparticles as both structural and active elements in self-assembling and self-healing multifunctional hydrogels for chronic wound management |
| dc.type | Article |
| dspace.entity.type | Publication |
| local.citation.author | Morena, A. G.; Perez, S.; Tzanov, T. |
| local.citation.endingPage | 20 |
| local.citation.number | 12, article 2658 |
| local.citation.publicationName | Pharmaceutics (Basel) |
| local.citation.startingPage | 1 |
| local.citation.volume | 14 |
| local.identifier.drac | 34925689 |
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