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Mao et al. Chem Synth 2023;3:26  https://dx.doi.org/10.20517/cs.2022.41         Page 23 of 33














































                Figure 14. (A) Schematic illustration of Cu E-based PTT and  RRT [184] , Copyright © American Chemical Society 2020; (B) Synthesis of
                                             2-x
                CSP-ACF nanoparticles and mechanism of CSP-ACF nanoparticles combined with X-rays in killing 4T1 tumors [185] , Copyright © American
                Chemical Society 2020; (C) The therapeutic functions of HMTCP@PFP@O  enhance radiosensitization in vivo [186] , Copyright © American
                                                                 2
                Chemical  Society  2020;  (D)  Schematic  representation  of  the  synthesis  of  nanomaterials  and  their  mechanisms  of  action  in
                radiotherapy [187] , Copyright © Wiley-VCH Verlag GmbH & Co. KGaA 2019. ACF: acriflavine; CSP: Cu Se@PtSe; CDT: chemodynamic
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                therapy; NIR: near-infrared region; PFP: perfluoropentane; RT: Radiation therapy; RRT: ROS-related therapy; VEGF: vascular endothelial
                growth factor.
               of checkpoint inhibitors, immune adjuvants, and CuS NPs. As shown in Figure 15D, an intelligent bio-
               inspired nanoplatform based on dendritic large pore mesoporous silica nanoparticles (DLMSNs), named
               AM@DLMSN@CuS/R848, was designed by Cheng et al. . Both CuS NPs with high PTT-conversion
                                                                 [149]
               efficiency and immune adjuvant (R848) were artfully embedded inside the macropores of DLMSNs, as
               shown in Figure 15E, and were utilized for the depression of metastatic tumors.

               Although the achievement of immunotherapy is sensational, its clinical applications were still inhibited by
               the immunosuppressive environment in the tumor. Immunotherapy approaches are often ineffective due to
               the highly complex immune suppression mechanisms in the TME and subjective deviations in patient
               reactions. Therefore, combining multiple immune activation mechanisms is considered to be the best
               strategy for tumor treatment. Among them, immunogenicity and/or immune-related adverse effects from
               antibody preparations, such as skin, gastrointestinal tract side effects, pneumonia, and hepatitis, were other
               challenges for the widespread clinical application of cancer IT. Therefore, there is an urgent requirement to
               identify effective synergetic strategies to improve the therapeutic efficacy while mitigating the systemic
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