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International Journal of Bioprinting                             3D-printed PCL-MNP multifunctional scaffolds




               When developing our PCL-MNP scaffolds, we aimed   hyperthermia experiments. Pure PCL and PCL with
            to (i) fabricate a biocompatible scaffold that aids in bone   50% MNP scaffolds were seeded with hMSCs and bone
            tissue regeneration by providing the necessary mechanical   cancer cells in respective glass vials. These scaffolds were
            support under physiological load and activating the   then cultured for 24 h in an incubator at 37°C. After 24
            correct signaling pathways, and (ii) target cancerous   h, the cell viability of the scaffolds was measured. After
            tumors  via  hyperthermia  treatment.  The  hyperthermia   the supernatant was collected in a 96-well plate and fresh
            capability of the scaffolds is evaluated by measuring the
            temperature rise when placed in an AMF (Figure 5A).   media replaced, the scaffolds were then placed in an AMF
            Figure 5B presents the temperature versus time graph for   for 2 h each, as depicted in the schematic in Figure 6A.
            all MNP concentrations in the PCL-MNP scaffolds. The   After 2 h, these glass vials were taken out and supplied
            peak temperature increases with increasing concentration   with AB to identify changes in viability after subjecting the
            of MNPs. For scaffolds with 50% MNPs, the average peak   seeded scaffolds to an AMF. From Figure 6B, a statistically
            temperature reached was more than 46 C.            significant decrease is observed in the proliferation of
                                           o
               For  the  scaffold  with  50%  MNPs,  the  temperature   cancer cells after 2 h, indicating that the increase in
            stabilized around 46°C, which is higher than the   temperature caused by the 50% MNP scaffold helped kill
            hypothermia threshold temperature required; hence,   the cancer cells. Conversely, the hMSCs exhibited increased
            the scaffold with 50% MNPs was used for subsequent   proliferation for the 50% MNP scaffold.
















































            Figure 5. Magnetization and hyperthermic measurements of PCL and PCL-MNP scaffolds. (A) Schematic of the process of a scaffold being placed in an
            alternating magnetic field, while the temperature is measured using a probe. (B) Temperature versus time graph. (C) Magnetization curves. Abbreviations:
            MNP, magnetic nanoparticle; PCL, polycaprolactone.


            Volume 10 Issue 6 (2024)                       400                                doi: 10.36922/ijb.4538
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