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International Journal of Bioprinting                                   Supramolecular hydrogels as bioinks




                                                                                                          (Continued...)

                    3D printing   method   N/A  N/A      N/A          N/A            N/A          N/A







                     Application  Drug delivery;   cell therapy; tissue   engineering  Synthetic ECM;   stem cell biology;   biomimetic;   bioinspired   synthetic materials  Biomedical   applications  Drug delivery   Biomedical   materials in   regenerative   medicine (e.g.,   cartilage repair)  Controlled drug   release







                   Self-   healing    property   Self-healable  Self-healable  Self-healable  No  Self-healable  No

                    Drug loading/   release  No  Controlled   release study of   70 kDa dextran   encapsulation  Controlled   release study of   70 kDa dextran   encapsulation   and hydrogel   erosion  Temperature-  mediated in   vitro release   kinetics studies   of HCPT  No  In vitro drug   release kinetics   (brimonidine in   PBS)







                 Rheological/  mechanical   properties  Mechanical   testing  Rheological   analysis: storage   modulus: -4.01   ± 0.01 kPa; loss   modulus: 0.49 ±   0.13 kPa  Stress relaxation   modulus: ~1 ×   10 4 −1 × 10 5  s   (~3−30 h); shear   thinning  Shear thinning  Viscoelastic   behavior: storage   modulus and   loss modulus  Rheological   analysis and   mechanical   properties   (compression,   tensile, cyclic   compression,   and anti-slicing   experiments)




             Table 1. Examples of supramolecular hydrogels and their applications in different areas
                    Reported   injectability   No  No    Yes         Yes, but not   tested  No    Yes





                     In vitro studies  No   No         NIH-3T3   fibroblasts; cell   viability studies  Hemolysis assay   and in vitro   cytotoxicity test   (CCK-8 assay);   LLC cells  Biocompatibility   test; mBMSC and   MDSC  Cytotoxicity   studies; NIH3T3   fibroblasts







                     In vivo studies   No  Mice; subcutaneous   implant  Hairless,   immunocompetent   SKH1-E mice;   encapsulation and   release of a model    macromolecule by in   vivo imaging  In vivo antitumor   activity on mice  No  No






                    Crosslinkage/  type   Non-covalent  Host–guest   chemistry; Click   reaction  Host–guest   chemistry;   photo-induced   covalent   dimerization  Host–guest   inclusion   complexation  Three-arm host–  guest chemistry;   UV-initiated   polymerization  Host–guest   chemistry










                    Polymer/  combination  Nor-seco-CB[10]   and adamantylamine   terminated-4-PEG 65  CB[7] and PEG 61  CB[8]-Pluronic   F-127 polymers 170  α-CD and binary-  drug-loaded micelles   (self-assembled   8-PEG-BA-HCPT) 85  β-CD-AOI2 and   A-TEG-Ad 42  4-PEG and α-CD 84



            Volume 10 Issue 3 (2024)                        21                                doi: 10.36922/ijb.3223
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