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Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications

Hyaluronic acid (HA) injectable biomaterials are currently applied in numerous biomedical areas, beyond their use as dermal fillers. However, bacterial infections and painful inflammations are associated with healthcare complications that can appear after injection, restricting their applicability....

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Autores principales: Andrade del Olmo, Jon, Pérez-Álvarez, Leyre, Sáez Martínez, Virginia, Benito Cid, Sandra, Pérez González, Raúl, Vilas-Vilela, José Luis, Alonso, José María
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033012/
https://www.ncbi.nlm.nih.gov/pubmed/35448124
http://dx.doi.org/10.3390/gels8040223
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author Andrade del Olmo, Jon
Pérez-Álvarez, Leyre
Sáez Martínez, Virginia
Benito Cid, Sandra
Pérez González, Raúl
Vilas-Vilela, José Luis
Alonso, José María
author_facet Andrade del Olmo, Jon
Pérez-Álvarez, Leyre
Sáez Martínez, Virginia
Benito Cid, Sandra
Pérez González, Raúl
Vilas-Vilela, José Luis
Alonso, José María
author_sort Andrade del Olmo, Jon
collection PubMed
description Hyaluronic acid (HA) injectable biomaterials are currently applied in numerous biomedical areas, beyond their use as dermal fillers. However, bacterial infections and painful inflammations are associated with healthcare complications that can appear after injection, restricting their applicability. Fortunately, HA injectable hydrogels can also serve as drug delivery platforms for the controlled release of bioactive agents with a critical role in the control of certain diseases. Accordingly, herein, HA hydrogels were crosslinked with 1 4-butanediol diglycidyl ether (BDDE) loaded with cefuroxime (CFX), tetracycline (TCN), and amoxicillin (AMX) antibiotics and acetylsalicylic acid (ASA) anti-inflammatory agent in order to promote antibacterial and anti-inflammatory responses. The hydrogels were thoroughly characterized and a clear correlation between the crosslinking grade and the hydrogels’ physicochemical properties was found after rheology, scanning electron microscopy (SEM), thermogravimetry (TGA), and differential scanning calorimetry (DSC) analyses. The biological safety of the hydrogels, expected due to the lack of BDDE residues observed in (1)H-NMR spectroscopy, was also corroborated by an exhaustive biocompatibility test. As expected, the in vitro antibacterial and anti-inflammatory activity of the drug-loaded HA-BDDE hydrogels was confirmed against Staphylococcus aureus by significantly decreasing the pro-inflammatory cytokine levels.
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spelling pubmed-90330122022-04-23 Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications Andrade del Olmo, Jon Pérez-Álvarez, Leyre Sáez Martínez, Virginia Benito Cid, Sandra Pérez González, Raúl Vilas-Vilela, José Luis Alonso, José María Gels Article Hyaluronic acid (HA) injectable biomaterials are currently applied in numerous biomedical areas, beyond their use as dermal fillers. However, bacterial infections and painful inflammations are associated with healthcare complications that can appear after injection, restricting their applicability. Fortunately, HA injectable hydrogels can also serve as drug delivery platforms for the controlled release of bioactive agents with a critical role in the control of certain diseases. Accordingly, herein, HA hydrogels were crosslinked with 1 4-butanediol diglycidyl ether (BDDE) loaded with cefuroxime (CFX), tetracycline (TCN), and amoxicillin (AMX) antibiotics and acetylsalicylic acid (ASA) anti-inflammatory agent in order to promote antibacterial and anti-inflammatory responses. The hydrogels were thoroughly characterized and a clear correlation between the crosslinking grade and the hydrogels’ physicochemical properties was found after rheology, scanning electron microscopy (SEM), thermogravimetry (TGA), and differential scanning calorimetry (DSC) analyses. The biological safety of the hydrogels, expected due to the lack of BDDE residues observed in (1)H-NMR spectroscopy, was also corroborated by an exhaustive biocompatibility test. As expected, the in vitro antibacterial and anti-inflammatory activity of the drug-loaded HA-BDDE hydrogels was confirmed against Staphylococcus aureus by significantly decreasing the pro-inflammatory cytokine levels. MDPI 2022-04-06 /pmc/articles/PMC9033012/ /pubmed/35448124 http://dx.doi.org/10.3390/gels8040223 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Andrade del Olmo, Jon
Pérez-Álvarez, Leyre
Sáez Martínez, Virginia
Benito Cid, Sandra
Pérez González, Raúl
Vilas-Vilela, José Luis
Alonso, José María
Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title_full Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title_fullStr Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title_full_unstemmed Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title_short Drug Delivery from Hyaluronic Acid–BDDE Injectable Hydrogels for Antibacterial and Anti-Inflammatory Applications
title_sort drug delivery from hyaluronic acid–bdde injectable hydrogels for antibacterial and anti-inflammatory applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033012/
https://www.ncbi.nlm.nih.gov/pubmed/35448124
http://dx.doi.org/10.3390/gels8040223
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