Page 14 - IJB-10-1
        P. 14
     International Journal of Bioprinting                                Magnetic (Bio)inks for tissue engineering
            Figure 1. Summary of the MNP synthesis techniques. (A) Co-precipitation: a basic solution is added to a solution with ferrous ions (i), inducing the
            precipitation of MNPs (ii) that are then attracted to a magnet (iii), washed (iv), and lyophilized (v). (B) Hydrothermal method: a basic solution is added to
            a solution with ferrous ions (i). The resulting solution is kept in an autoclave at high temperature and pressure (ii) to control the formation of MNPs, which
            are then filtered (iii), dried, and pulverized (iv). (C) Thermal decomposition (heating-up): precursor reagents are mixed under an inert gas atmosphere at
            high temperatures, under reflux; after heating the mixture to the boiling point of the solvent and the decomposition point of the precursors, crystals form
            and, after a growth phase, the MNPs are obtained.
            polymeric matrix due to its convenience and procedural   bioink composition for bioprinting of magnetically-
            simplicity.  In  this  approach,  the  MNPs  are  prepared   responsive structures. 22
            separately from the hydrogel and are then dispersed in
            the pre-crosslinked hydrogel solution, often resorting   3.2. Grafting-onto method
            to sonication to achieve good dispersion in the solution   In the grafting-onto method, MNPs are also embedded
            (Figure 2A).                                       in the hydrogel solution before the crosslinking process
                                                               takes place. However, in this method, functional groups
               Despite the advantages of this approach, the fact that   are grafted onto the particles prior to their mixing with
            the particles are not strongly bound to the polymeric   the solution  (Figure 2B). These functional groups
                                                                         41
            chains can cause them to diffuse out of the hydrogel,    then interact with the polymeric chains of the hydrogel
                                                         42
            as well as lead to an uneven particle distribution   during crosslinking, working to create bonds with the
            throughout the polymeric matrix.  Furthermore, the   hydrogel, and thus MNPs become an integral part of the
                                         10
            particles can aggregate, which is generally unwanted in   overall structure.
            biomedical applications, potentially lead to toxicity,
                                                         43
            and affect their efficiency, for example, decreasing their   This technique allows for a more uniform dispersion
            hyperthermic ability, which is very important for cancer   and better stability of the MNPs within the polymeric
            therapies.  This type of approach has been used in   matrix. Nevertheless, the functionalization of the
                    44
            various studies, to obtain magnetic hydrogels targeting   nanoparticles  is  very  time-consuming,  costly,  and
            several purposes, such as the fabrication of anisotropic   complex.  This method was reported by Hu et al.  who
                                                                      41
                                                                                                        46
            structures,  drug delivery systems, and bone tissue   fabricated adhesive, tough, and strong polyacrylamide
                     45
            engineered structures  as well as the optimization of   hydrogels, with a concentration of MNPs as high as 60%,
                              4
            Volume 10 Issue 1 (2024)                        6                          https://doi.org/10.36922/ijb.0965





