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International Journal of Bioprinting                      3D-printed thermosensitive hydrogel based microrobots















































            Figure 8. (a) 3D printing window of PNAGA-100-encapsuled DOX. (b) 3D structures of PNAGA-100-DOX printed via 2PP method. (c) DOX release
            measurement of PNAGA-100 under 25°C and 45°C, respectively. (d) Evaluation of thermosensitive properties of PNAGA-100.

            concentration  benefits  the  formation  in  a  longer  term   microstructures that encapsule DOX as drugs were
            and orderly hydrogen network when the temperature   3D-printed via the 2PP method. Figure 8a shows the 3D
            is increased, and thus exhibits better thermosensitive   printing window of PNAGA-100-DOX with varying laser
            performance than PNAGA-50. However, in the region with   powers and scan speeds. Taking laser power of 90 mW and
            a high concentration of NAGA (above 10 wt%) referred   scan speed of 3000 μm/s as an example, 3D structures of
            to as Region 2 in  Figure 7, high-strength and robust   PNAGA-100-DOX in the shape of a five-pointed star with
            supramolecular PNAGA hydrogels, which are equipped   clear outlines were printed, proving that 3D printing of
            with nonthermosensitive and nonswellable features,   PNAGA-100-based thermosensitive microstructure with
            were obtained . As a result, PNAGA-100 with medium   DOX via 2PP method can be successfully achieved with
                       [27]
            NAGA concentration  manifests better thermosensitive   perfect 3D configuration (Figure 8b). Second, PNAGA-100-
            performance than PNAGA-200 and PNAGA-300 with      DOX based microstructures were incubated in DI water at
            high-strength  supramolecular  networks.  In  terms  of   45°C and 25°C, respectively. The DOX release amount was
            practical applications, different PNAGA systems can be   evaluated by measuring the absorbance using a microplate
            selected based on the requirements by varying the NAGA   reader. As displayed in Figure 8c, the DOX release amounts
            concentrations.                                    of PNAGA-100 at 45°C are about two to three times higher
                                                               than that at 25°C under each incubation time, which agrees
            3.5. Drug release                                  well with its thermosensitive performance (Figure 8d). At
            Taking  into  account  the  excellent  thermosensitive   45°C, higher DOX release amounts were observed, which
            performance of PNAGA-100, the drug release         may be due to the swelling state of PNAGA-100, benefiting
            measurements were assessed with PNAGA-100 under    the expansion of the porous structures on the surface of
            45°C and 25°C, respectively. Firstly, PNAGA-100    PNAGA-100-based hydrogels and thus contributing to

            Volume 9 Issue 3 (2023)                        279                         https://doi.org/10.18063/ijb.709
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