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Wang et al. Microstructures 2023;3:2023042  https://dx.doi.org/10.20517/microstructures.2023.46  Page 7 of 16

               Table 1. Magnetic thermal property of Fe O  NPs in different matrices under AMF irradiation [Mean ± SD (n = 3)]
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                                                                          ΔT of gelatin
                                          ΔT of agarose   Percentage compared          Percentage compared
                Sample       ΔT of PBS (°C)                               porous scaffold
                                          hydrogel (°C)  to free NPs      (°C)         to free NPs
                No Fe O  NPs  0.7 ± 0.2   1.0 ± 0.2    /                  0.8 ± 0.2    /
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                   3
                         -1
                Fe O -5 mg mL  24.1 ± 1.7  14.0 ± 0.3  58.1%              5.2 ± 0.3    21.6%
                 3  4
                          -1
                Fe O -10 mg mL  38.3 ± 1.1  22.8 ± 1.7  59.5%             9.1 ± 0.5    23.8%
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                   4
                Fe O -20 mg mL -1  65.7 ± 1.4  33.8 ± 1.0  51.5%          13.2 ± 0.4   20.1%
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                Figure 2. TEM images of citrate-modified Fe O  NPs at low (A), middle (B), and high magnifications (C). Hydrodynamic size
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                distribution of citrate-modified Fe O  NPs (D).
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               The free Fe O  NPs in PBS showed the highest temperature change. The temperature change was reduced to
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               51.5%-59.5% when the Fe O  NPs were embedded in agarose hydrogels. The temperature change was
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               further decreased to 20.1%-23.8% when the Fe O  NPs were embedded in gelatin porous scaffolds. The
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               results indicated that the matrix where Fe O  NPs were embedded could significantly affect the magnetic-
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               thermal conversion property of Fe O  NPs.
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               Anticancer effect of free Fe O  NPs
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               MH uses the Fe O  NPs to absorb and convert magnetic energy to heat and raise the local temperature,
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               thereby killing the cancer cells. In this study, MDA-MB-231-Luc cells were cultured in a culture medium
               supplemented with free Fe O  NPs under different concentrations. Cell viability before and after AMF
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               irradiation was investigated by live/dead staining and WST-1 assay [Figure 5]. Before AMF irradiation,
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