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Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing
Two antimicrobial agents such as silver nanoparticles (AgNPs) and titanium dioxide (TiO(2)) have been formulated with natural polysaccharides (chitosan or alginate) to develop innovative inks for the rapid, customizable, and extremely accurate manufacturing of 3D-printed scaffolds useful as dressing...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376448/ https://www.ncbi.nlm.nih.gov/pubmed/37508200 http://dx.doi.org/10.3390/antibiotics12071104 |
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author | Remaggi, Giulia Bergamonti, Laura Graiff, Claudia Ossiprandi, Maria Cristina Elviri, Lisa |
author_facet | Remaggi, Giulia Bergamonti, Laura Graiff, Claudia Ossiprandi, Maria Cristina Elviri, Lisa |
author_sort | Remaggi, Giulia |
collection | PubMed |
description | Two antimicrobial agents such as silver nanoparticles (AgNPs) and titanium dioxide (TiO(2)) have been formulated with natural polysaccharides (chitosan or alginate) to develop innovative inks for the rapid, customizable, and extremely accurate manufacturing of 3D-printed scaffolds useful as dressings in the treatment of infected skin wounds. Suitable chemical–physical properties for the applicability of these innovative devices were demonstrated through the evaluation of water content (88–93%), mechanical strength (Young’s modulus 0.23–0.6 MPa), elasticity, and morphology. The antimicrobial tests performed against Staphylococcus aureus and Pseudomonas aeruginosa demonstrated the antimicrobial activities against Gram+ and Gram− bacteria of AgNPs and TiO(2) agents embedded in the chitosan (CH) or alginate (ALG) macroporous 3D hydrogels (AgNPs MIC starting from 5 µg/mL). The biocompatibility of chitosan was widely demonstrated using cell viability tests and was higher than that observed for alginate. Constructs containing AgNPs at 10 µg/mL concentration level did not significantly alter cell viability as well as the presence of titanium dioxide; cytotoxicity towards human fibroblasts was observed starting with an AgNPs concentration of 100 µg/mL. In conclusions, the 3D-printed dressings developed here are cheap, highly defined, easy to manufacture and further apply in personalized antimicrobial medicine applications. |
format | Online Article Text |
id | pubmed-10376448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103764482023-07-29 Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing Remaggi, Giulia Bergamonti, Laura Graiff, Claudia Ossiprandi, Maria Cristina Elviri, Lisa Antibiotics (Basel) Article Two antimicrobial agents such as silver nanoparticles (AgNPs) and titanium dioxide (TiO(2)) have been formulated with natural polysaccharides (chitosan or alginate) to develop innovative inks for the rapid, customizable, and extremely accurate manufacturing of 3D-printed scaffolds useful as dressings in the treatment of infected skin wounds. Suitable chemical–physical properties for the applicability of these innovative devices were demonstrated through the evaluation of water content (88–93%), mechanical strength (Young’s modulus 0.23–0.6 MPa), elasticity, and morphology. The antimicrobial tests performed against Staphylococcus aureus and Pseudomonas aeruginosa demonstrated the antimicrobial activities against Gram+ and Gram− bacteria of AgNPs and TiO(2) agents embedded in the chitosan (CH) or alginate (ALG) macroporous 3D hydrogels (AgNPs MIC starting from 5 µg/mL). The biocompatibility of chitosan was widely demonstrated using cell viability tests and was higher than that observed for alginate. Constructs containing AgNPs at 10 µg/mL concentration level did not significantly alter cell viability as well as the presence of titanium dioxide; cytotoxicity towards human fibroblasts was observed starting with an AgNPs concentration of 100 µg/mL. In conclusions, the 3D-printed dressings developed here are cheap, highly defined, easy to manufacture and further apply in personalized antimicrobial medicine applications. MDPI 2023-06-25 /pmc/articles/PMC10376448/ /pubmed/37508200 http://dx.doi.org/10.3390/antibiotics12071104 Text en © 2023 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 Remaggi, Giulia Bergamonti, Laura Graiff, Claudia Ossiprandi, Maria Cristina Elviri, Lisa Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title | Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title_full | Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title_fullStr | Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title_full_unstemmed | Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title_short | Rapid Prototyping of 3D-Printed AgNPs- and Nano-TiO(2)-Embedded Hydrogels as Novel Devices with Multiresponsive Antimicrobial Capability in Wound Healing |
title_sort | rapid prototyping of 3d-printed agnps- and nano-tio(2)-embedded hydrogels as novel devices with multiresponsive antimicrobial capability in wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376448/ https://www.ncbi.nlm.nih.gov/pubmed/37508200 http://dx.doi.org/10.3390/antibiotics12071104 |
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