2022
DOI: 10.1016/j.colsurfa.2022.128329
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3D-printed high-toughness double network hydrogels via digital light processing

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Cited by 11 publications
(4 citation statements)
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“…During the UV light-induced polymerization process, in situ formation of carboxyl-Zr 4+ coordination crosslinking and LMA hydrophobic association crosslinking occurred, endowing the hydrogel materials with a cohesive and integral network structure. [23][24][25] Throughout the incubation period in water, this cross-linked network was further strengthened on account of the generation of electrostatic interactions and the structural reconfiguration of the coordination complexes. More specifically, during the incubation of the pre-hydrogels in water, the electrostatic interactions between the N + of CTAB and the COO À on PAA chains gradually emerged, which was attributed to the partial ionization of AAc units accompanying the increase in pH.…”
Section: Resultsmentioning
confidence: 99%
“…During the UV light-induced polymerization process, in situ formation of carboxyl-Zr 4+ coordination crosslinking and LMA hydrophobic association crosslinking occurred, endowing the hydrogel materials with a cohesive and integral network structure. [23][24][25] Throughout the incubation period in water, this cross-linked network was further strengthened on account of the generation of electrostatic interactions and the structural reconfiguration of the coordination complexes. More specifically, during the incubation of the pre-hydrogels in water, the electrostatic interactions between the N + of CTAB and the COO À on PAA chains gradually emerged, which was attributed to the partial ionization of AAc units accompanying the increase in pH.…”
Section: Resultsmentioning
confidence: 99%
“…As illustrated in Figure 3j, the fracture strength and Young's modulus of various DLP 3D printing hydrogels are summarized on an Ashby plot for comparison with the resilience hydrogels with tissue‐like softness. Remarkably, the fracture strength and Young's modulus of the springiness hydrogels in this work are much higher than those of various DLP 3D printed hydrogels such as P(DMAEMA‐MAA) hydrogel, [ 21 ] AAm‐PEGDA hydrogel, [ 22 ] GMHA‐PSPA hydrogel, [ 23 ] PSMA double‐network (DN) hydrogel, [ 24 ] MA‐Starch hydrogel, [ 25 ] PEG‐DA hydrogel, [ 26 ] GelMA hydrogel, [ 27 ] Sil‐MA hydrogel, [ 28 ] and HG hydrogel. [ 29 ] It can be seen that the stiffness of the resilience hydrogels is mechanically tunable in a wide range from a few kilopascals to hundreds of kilopascals, thus providing promising candidates for the fabrication of structurally sophisticated multiple soft tissue mimics.…”
Section: Resultsmentioning
confidence: 99%
“…Finally, Figure 6h offers insight into the stress-strain curves of the self-healed hydrogels, showcasing their performance over increasing healing durations. Zhang et al [90] experimented with Antheraea pernyi silk fibroin bioinks for DLP 3D printing, offering new opportunities in bioprinting and regenerative medicine. In another innovative stride, Xiang et al [91] focused on creating 3D-printed high-toughness double network hydrogels via DLP, contributing to the development of mechanically robust hydrogel materials.…”
Section: Digital Light Processing (Dlp)mentioning
confidence: 99%