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Advances in Radiotherapy
            & Nuclear Medicine                                              Nanomaterials in cancer chemoimmunotherapy



            the immunogenic inducer paclitaxel and indoleamine   due to their excellent characteristics, including non-
            2,3-dixoygenase 1 blocker 1-methyl-D,L-tryptophan. The   immunogenicity, good stability, ease of synthesis, ease
            polymeric nanocarriers were composed of poly(ethylene   of functionalization, inertness, and high drug-loading
            glycol) as the hydrophilic segment, with enzyme    capacity. In addition, some nanoparticles exhibit
            cleavable 1-methyl-D,L-tryptophan ester, and oxidation-  remarkable magnetic, thermal, and optical properties,
            sensitive phenyl peroxalate ester as hydrophobic blocks.    while others can be designed in various sizes, structures,
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            The copolymer self-assembles into prodrug-based    and geometries, such as nanorods, nanospheres,
            nanoparticles, which release paclitaxel in response to   nanoshells, and nanostars. Numerous metallic and
            intracellular ROS, thereby inducing immunogenic cell   inorganic nanoparticles have been studied as nanovectors
            death. The generated ROS further promotes nanoparticle   for delivering therapeutics to targeted tumor sites in
            disassembly and the continued release of paclitaxel,   chemoimmunotherapy. For example, gold nanoparticle
            enhancing the therapeutic effects.                 vesicles co-loaded with the immune inhibitor BLZ-
                                                               945 and the anticancer drug SN38 were developed for

            4.3. Dendrimers                                    chemoimmunotherapy against primary and metastatic
            Dendrimers are well-known drug nanocarriers with   cancers, incorporating photoacoustic imaging in the
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            both hydrophobic and hydrophilic components. They   second near-infrared window.  The gold nanoparticle
            are hyperbranched, spherical polymers that can be easily   vesicles were synthesized through the self-assembly
            functionalized through surface conjugation and exhibit   of  nanogapped  gold  nanoparticles  with  poly(ethylene
            stable structures at all concentrations.  Their unique   glycol) and poly(SN38-co-4-vinylpyridine). The vesicles
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            properties – including hydrophobic or hydrophilic   exhibited dual biologically responsive properties, being
            cavities in the interior, well-defined structure, size   both pH-  and redox-sensitive. In another study, a
            monodispersity, compact globular shape, numerous   multifunctional nanoparticle formulation with an iron
            internal cavities, a  large number  of controllable   oxide core was developed as a nanovector for the targeted
            “peripheral” functionalities, good versatility, high water   and simultaneous co-delivery of the cytotoxic agent
            solubility, superior biocompatibility, and high ratio of   doxorubicin and TLR3 agonist polyinosinic: polycytidylic
            surface groups to molecular volume – make dendrimers   acid to both breast cancer and dendritic cells. This
            excellent drug delivery vectors. Due to their unique   formulation utilized an endoglin-binding peptide
            structure and properties, drug molecules can either   to  target  both  triple-negative  breast  cancer  cells  and
            be physically encapsulated in the internal cavities of   vasculature endothelium.  The nanoparticles induced
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            dendrimers through non-covalent interactions or    tumor apoptosis through multiple mechanisms, such
            chemically conjugated to the peripheral functional groups   as direct cancer cell killing and dendritic cell-mediated
            through covalent interactions. In addition, the peripheral   innate and T cell-mediated adaptive immune responses.
            functional groups allow for the attachment of different   Recently, black phosphorus nanoparticles were co-loaded
            solubilizing groups and targeting moieties on the surface   with  low-dose doxorubicin  and BMS-202  (a  PD-L1
            in a multivalent fashion. Dendrimeric products such as   blocker) for the chemoimmunotherapy of lung cancer.
                 ®
            Stratus  CS Acute Care Diagnostic System and Starburst    Drug  release  from  the  composite  occurred  upon  mild
                                                         ®
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            have  already  been  approved  by the  FDA  and  are   photothermal heating at 40°C.  In this system, low-
            commercially available for healthcare.  Both of these are   dose doxorubicin-induced oxidative stress and activated
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            tectodendrimers, which are superstructured dendrimers   the high mobility group box 1/receptor for advanced
            with a high-generation core and low-generation shell.   glycation end product/nuclear factor kappa light chain
            Recently, Song  et al.  developed pH-sensitive core-  enhancer of activated B cells/PD-L1 pathway. The drug-
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            shell tectodendrimers for the simultaneous co-delivery   loaded composite demonstrated improved cancer cell
            of CD47 siRNA and doxorubicin to tumor cells for   toxicity and promising synergism in the presence of
            synergistic chemoimmunotherapy of breast cancer. The   tumor-associated macrophages.
            developed nanovector could simultaneously compress
            siRNA and physically load doxorubicin with good loading   4.5. Biomimetic nanoparticles
            efficacy, and it could rapidly release the drug in the acidic   Biomimetic nanoparticles, which are prepared by mixing
            tumor microenvironment.                            or coating biocompatible materials with biomaterials to
                                                               mimic the functions of natural structures and processes,
            4.4. Metallic and inorganic nanoparticles
                                                               can camouflage themselves as autologous components.
            Metallic and inorganic nanoparticles have been widely   These features allow them to circumvent rapid clearance
            utilized  as  nanocarriers  for  delivering  therapeutics   by the immune system, thereby prolonging circulation


            Volume 3 Issue 1 (2025)                         87                             doi: 10.36922/arnm.8150
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