Hybrid Hydrogels with Orthogonal Transient Cross-linking Exhibiting Highly Tunable Mechanical Properties AITranslate
Abstract AITranslate
Compositional changes in the chemical makeup of hydrogels offer a powerful strategy for fine tuning of mechanical properties, enabling specific targeting for different applications. The chemical versatility exhibited by the tunable system introduced here can be leveraged to address a broad range of characteristics across the field of tissue engineering─from blood vessels to cartilage, for example─which demands materials with very different mechanical profiles. Furthermore, we rely exclusively on dynamic, non-covalent cross-linking to provide opportunities for 3D printing and injectability. This work describes a highly tunable system based on hydrogen bonding and ionic interactions. Single network hydrogels were made by exploiting various acrylic monomers including N-acryloyl glycinamide (NAGA) and acrylic acid (AAc). Additionally, hybrid hydrogels were explored by combining these acrylic networks with an ionically cross-linked alginate network. By combining orthogonal cross-linking strategies and altering the ratio between different components in these hybrid gels, a broad range of mechanical properties is demonstrated. The characteristics were extensively investigated using tensile testing, compression testing, and rheological measurements. The final scaffolds were also shown to be non-cytotoxic in preliminary cell viability studies for human dermal fibroblasts.
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DOI:https://doi.org/10.1021/acsapm.2c01906
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Compositional changes in the chemical makeup of hydrogels offer a powerful strategy for fine tuning of mechanical properties, enabling specific targeting for different applications. The chemical versatility exhibited by the tunable system introduced here can be leveraged to address a broad range of characteristics across the field of tissue engineering─from blood vessels to cartilage, for example─which demands materials with very different mechanical profiles. Furthermore, we rely exclusively on dynamic, non-covalent cross-linking to provide opportunities for 3D printing and injectability. This work describes a highly tunable system based on hydrogen bonding and ionic interactions. Single network hydrogels were made by exploiting various acrylic monomers including N-acryloyl glycinamide (NAGA) and acrylic acid (AAc). Additionally, hybrid hydrogels were explored by combining these acrylic networks with an ionically cross-linked alginate network. By combining orthogonal cross-linking strategies and altering the ratio between different components in these hybrid gels, a broad range of mechanical properties is demonstrated. The characteristics were extensively investigated using tensile testing, compression testing, and rheological measurements. The final scaffolds were also shown to be non-cytotoxic in preliminary cell viability studies for human dermal fibroblasts.
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| GB/T 7714-2015 | [1] Sofie Houben, Ana A. Aldana, AnSofie Huysecom, et al. ACS Applied Polymer Materials, 2023(5). DOI:10.1021/acsapm.2c01906. |
| MLA | [1] Sofie Houben, et al., ACS Applied Polymer Materials, no. 5, 2023, https://doi.org/10.1021/acsapm.2c01906. |
| APA | [1] Sofie Houben, Ana A. Aldana, AnSofie Huysecom, Winy Mpinganzima, Ruth Cardinaels, Matthew B. Baker, & Louis M. Pitet. (2023). ACS Applied Polymer Materials(5). https://doi.org/10.1021/acsapm.2c01906 |
| IEEE | [1] Sofie Houben, Ana A. Aldana, AnSofie Huysecom, Winy Mpinganzima, Ruth Cardinaels, Matthew B. Baker, and Louis M. Pitet, ACS Applied Polymer Materials, no. 5, 2023, doi: 10.1021/acsapm.2c01906. keywords: {interpenetrating network hydrogels;hybrid hydrogels;dynamic crosslinking;tissue engineering} |
