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Au-Pt Nanoparticle Formulation as a Radiosensitizer for Radiotherapy with Dual Effects

Authors Yang S, Han G, Chen Q, Yu L, Wang P, Zhang Q, Dong J, Zhang W, Huang J

Received 22 October 2020

Accepted for publication 18 December 2020

Published 12 January 2021 Volume 2021:16 Pages 239—248


Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 3

Editor who approved publication: Dr Mian Wang

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Song Yang, 1, 2,* Gaohua Han, 1, 2,* Quan Chen, 2, 3 Lei Yu, 1, 2 Peng Wang, 1, 2 Qi Zhang, 1, 2 Jiang Dong, 1, 2 Wei Zhang, 2, 4 Junxing Huang 1, 2

1Department of Oncology, Taizhou People’s Hospital, Taizhou, Jiangsu, People’s Republic of China; 2Medical School of Nantong University, Nantong, Jiangsu, People’s Republic of China; 3Department of Thoracic Surgery, Taizhou People’s Hospital, Taizhou, Jiangsu, People’s Republic of China; 4Department of Infectious Disease, Taizhou People’s Hospital, Taizhou, Jiangsu, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Wei Zhang
Department of Infectious Disease, Taizhou People’s Hospital, No. 399, South Hailing Road, Taizhou, 225300 Jiangsu, People’s Republic of China
Tel +86-523-86606739
Email [email protected]
Junxing Huang
Department of Oncology, Taizhou People’s Hospital, No. 399, South Hailing Road, Taizhou, 225300 Jiangsu, People’s Republic of China
Tel +86-523-86606739
Email [email protected]

Background: Radiotherapy occupies an essential position as one of the most significant approaches for the clinical treatment of cancer. However, we cannot overcome the shortcoming of X-rays which is the high value of the oxygen enhancement ratio (OER). Radiosensitizers with the ability to enhance the radiosensitivity of tumor cells provide an alternative to changing X-rays to protons and heavy ion radiotherapy.
Materials and Methods: We prepared the Au-Pt nanoparticles (Au-Pt NPs) using a one-step method. The characteristics of the Au-Pt NPs were determined using TEM, HAADF-STEM, elemental mapping images, and DLS. The enhanced radiotherapy was demonstrated in vitro using MTT assays, colony formation assays, fluorescence imaging, and flow cytometric analyses of the apoptosis. The biodistribution of the Au-Pt NPs was analyzed using ICP-OES, and thermal images. The enhanced radiotherapy was demonstrated in vitro using immunofluorescence images, tumor volume and weigh, and hematoxylin & eosin (H&E) staining.
Results: Polyethylene glycol (PEG) functionalized nanoparticles composed of the metallic elements Au and Pt were designed to increase synergistic radiosensitivity. The mechanism demonstrated that heavy metal NPs possess a high X-ray photon capture cross-section and Compton scattering effect which increased DNA damage. Furthermore, the Au-Pt NPs exhibited enzyme-mimicking activities by catalyzing the decomposition of endogenous H 2O 2 to O 2 in the solid tumor microenvironment (TME).
Conclusion: Our work provides a systematically administered radiosensitizer that can selectively reside in a tumor via the EPR effect and enhances the efficiency of treating cancer with radiotherapy.

Keywords: radiosensitizer, nano-enzyme, TME, radiotherapy


Radiation therapy (radiotherapy, RT) is one of the most effective therapies available for the treatment of localized solid cancers.1 During radiotherapy of a malignant tumor, biological macromolecules of the tumor cells directly interact with the radiation to generate free radicals which cause damage to the DNA, such as strand breaks, point mutations, and aberrant DNA cross-linking.2–4 In addition, the radiation causes water molecules in the tissues to ionize and produce free radicals, which in turn interact with the biological macromolecules to cause cell damage and death.5 Theoretically, almost all types of tumors could be effectively controlled when the local radiation dose is high enough.6 However, a high dose of radiation induces high toxicity to healthy tissues causing side effects.7 Except for the new radiation-delivery techniques that improved the therapeutic effect, highly effective and low-toxicity radiosensitizers are necessary. The improvement of the physical technology, for example, brachytherapy, intensity-modulated RT, image-guided RT, and stereotactic RT has greatly improved radiation therapy.8–11 However, many problems still remain, such as the complex tumor microenvironment containing cancer stem cells, vasculogenesis, and metabolic alterations.12–14

Except for tumor size, the intrinsic radio-sensitivity, cell proliferation, and the extent of hypoxia are important factors for controlling the tumor.15 Hypoxia is one of the most important indicators and is related to cancer therapy-resistance.16 Hypoxia activates the Nrf2 pathway, which leads to anti-oxidant and anti-inflammatory responses with an aggregation of M2 macrophages and MDSCs that protect the tumor.5 Owing to the existence of the hypoxic microenvironment of the tumor, the therapeutic efficiency of chemotherapy, radiotherapy and others, are reduced. In recent years, different strategies including physical stimulation (e.g. fractional irradiation) and chemical reaction, have been developed for relieving tumor hypoxia.17,18 However, it is difficult to prevent the growth of a tumor using a monotherapy. Due to the reduced side effects and enhanced therapeutic effect of synergistic therapy, it is used to overcome the insufficient tumor suppression effect of monotherapy.

Radiosensitizers are molecules/materials with the ability to enhance the radiosensitivity of tumor cells and provide opportunities to overcome the obstacles mentioned above.2 There are many kinds of radiosensitizers, namely small-molecule chemicals, macromolecules, and nanostructures.19 One of the most important mechanisms for increasing radiosensitivity is to change the hypoxic microenvironment via different kinds of radiosensitizers. Many tumors are resistant to radiation therapy because they lack oxygen within the tumor due to abnormal or dysfunctional blood vessels.20 This state of hypoxia leads to less DNA damage at the same radiation dose.21 Therefore, oxygen is a well-known radiosensitizer.4 Chemicals and hypoxia-inducing cytotoxins were developed for clinical use because of their oxygen-producing capacity through a mechanism of damage fixation utilizing their electron affinity.22,23 Macromolecules are able to regulate the radio-sensitivity mechanism by binding with the DNAs, miRNA, mRNAs, siRNAs, proteins or peptides.24 Recently, the introduction of nanotechnology has provided momentum and expanded the horizon for the development of radiosensitizers.25 In recent years, heavy-metal nanomaterials with high atomic numbers (Z) have shown promise as radiosensitizers because they can absorb, scatter, and emit radiation energy.26–28 An excellent candidate is gold nanomaterials (AuNPs) because they have tunable morphologies, they are easy to modify, they have good biological safety, and they have exceptional radiation sensitization capabilities.29–32 Furthermore, AuNPs are good for drug delivery and cancer therapy.33 In addition, various catalase-like nanomaterials have been developed for catalyzing the decomposition of hydrogen peroxide (H2O2) into oxygen, which alleviates tumor hypoxia, and overcomes the hypoxia-induced radioresistance.34 Therefore, to develop a simple and effective strategy for relieving the hypoxic tumor microenvironment is essential to improving the therapeutic efficacy of radiotherapy.

In the present study, we designed a nanoparticle composed of the metallic elements Au and Pt (Au-Pt NPs). The Au-Pt NPs exhibited enzyme-mimicking activities, which resulted in synergistic radiosensitivity for reinforced tumor therapy. The new Au-Pt NPs with nanozymes were synthesized in one step at room temperature. The nanoparticles produced had a uniform nanosphere shape and were very stable in physiological solutions. After intravenous administration, the Au-Pt NPs passively targeted the tumor and rapidly accumulated in it because of the enhanced permeability and retention (EPR) effect. Not only do the Au-Pt nanozymes possess a radiosensitivity ability to enhance the energy deposition of the X-rays but are also able to catalyze the reaction that converts H2O2 to O2. In addition to attenuating tumor hypoxia, the Au-Pt NPs significantly inhibited tumor growth under 8 Gy of X-ray irradiation compared to the control group. This demonstrated that the Au-Pt NPs improved the therapeutic efficiency of radiotherapy. Therefore, our work developed a novel radiosensitizer with low toxicity, for enhanced tumor radiotherapy by alleviating the tumor hypoxic microenvironment. Our findings highlight the great potential of applying Au-Pt NPs in the future clinical treatment of cancer.

Materials and Methods

Synthesis of Au-Pt NPs

L-proline 0.0384 g, 20 μL of HAuCl4 and H2PtCl6 solution (1mol/L) were dispersed in 10 mL of deionized water. The pH value of the solution was adjusted to 9 by adding NaOH. Next, ascorbic acid (10 mmol L−1) was added drop by drop. The products were obtained by allowing the solution to react for 20 min at room temperature. Finally, C18PMH-PEG (10 mg) was added to 10 mL of an Au-Pt solution. Au-Pt-PEG-PMH was obtained by stirring the solution for 24 h at room temperature. After 2 h of ultrasonication, the mixture was dried by rotary evaporator. Ten mL of deionized water was added to dissolve the solid which yielded PEGylated Au-Pt nanoparticles (Au-Pt NPs). The Au-Pt nanoparticle that were obtained were further purified through centrifugation at 6000 rpm for 10 min to remove any incompatible nanomaterials. In addition, the Au-Pt NPs were washed three times through ultrafiltration filters with 100 kDa MWCO to remove any unbound PEG.

Determining the Characteristics of the Au-Pt NPs

The hydrodynamic diameters and Zeta potentials of the Au-Pt NPs suspended in PBS and 10% FBS were measured by dynamic light scattering (DLS) (Malvern Instruments, UK). The morphology was determined using high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), and the characteristics were described from elemental mapping images using a transmission electron microscope (TEM, JEM-1230, Japan).

Detection of O2

To investigate the efficiency with which oxygen is generated in vitro, the Au-Pt NPs (50 μg/mL), H2O2 (2 mmol/L) were added to 3 mL of PBS (pH 6.75) at room temperature. An oxygen probe (JPBJ-608 portable Dissolved Oxygen Meters, Shanghai REX Instrument Factory) was used to measure the dissolved oxygen concentration every minute for 18 minutes.

Cell Line and Animals

Cells of the human vascular endothelial cell line HUEVC and murine breast cancer cell line 4T1 were provided by the central laboratory of Taizhou People’s Hospital (purchased from the Cell Bank, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai) and grown in the recommended cell culture medium under the standard conditions. Female BALB/c mice (6–8 weeks) were maintained according to the protocols approved by the Nantong University Laboratory Animal Center. All animal protocols were in accordance with the National Institute’s Health Guide for the Care and Use of Laboratory Animals.

In vitro Cell Experiments

The cell cytotoxicity was determined by the 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay (Sigma) following the standard protocol. The surviving fraction (SF) of the clone formation assay was calculated after the cells were irradiated with 0, 2, 4, 6 or 8 Gy X-rays and kept in culture for 10 days. Fluorescence images were obtained of the phosphorylated H2AX (γH2AX) in the 4T1 murine breast cancer cells after irradiation for 24 h and treated with Au-Pt NPs. The radiation source was a RS 2000 with 0.3 mm copper filter, irradiating at 160 kV at 25 mA and a dose rate of 1.203 Gy/min. The fluorescence images were analyzed using Living Imaging software. Live/dead cell discrimination was performed using the Live/Dead Fixable Aqua Dead Cell Stain Kit (Life Technologies) or the Sytox Red Dead Cell Stain (Life Technologies). Cell surface staining was done for 20–30 minutes. Cells were spun down and stained with a 1:200 final concentration of the antibodies in 50% of a 2.4G2 (Fc block) and 50% of a FACS Buffer (PBS + 1% FBS, 2mM EDTA) for 15 min. Flow cytometric analyses were performed to determine the percentage of apoptotic cells. Cells suspended in PBS containing 1% FBS were incubated with anti-mouse antibody against Annexin V-FITC and PI for 20 min at room temperature in the dark and then evaluated using a flow cytometer. All flow cytometry analyses were performed using an LSRFortessa (BD Biosciences) or an LSR-II (BD Biosciences). The flow data were analyzed using FlowJo v.10 (Tree Star, Inc.).

Pharmacokinetic Parameters and Biodistribution in vivo

At different points in time, post injection of the Au-Pt NPs, 20 μL of blood was drawn from the right orbital venous plexus for the Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) analysis. The ICP-OES signals in blood samples were measured using a gamma counter. At 24 h post injection, the mice were sacrificed, and all major organs and tumors were collected. Then, fluorescence of organs and tumors were measured using a gamma counter. In vivo CT imaging, 100 μL of PBS and 100 μL of Au-Pt NPs (20 mg/kg) were injected into the tumor site in situ. Mice were anesthetized and scanned using a Philips CT imager. CT images were obtained from the Philips 256 CT scanning system.

Antitumor Efficacy in vivo

The 4T1 tumor-bearing BALB/c mice were randomly allocated to four groups: (a) control group (PBS); (b) Au-Pt NPs; (c) X-ray; (d) Au-Pt NPs + X-ray. When the tumor volume reached 60 mm3 at 24 h post-injection of PBS and Au-Pt NPs (20 mg/kg), the mice were exposed to X-ray (8 Gy). The tumor sizes and weight were recorded every other day after treatment. The mice were defined as dead when the tumor volume exceeded 1000 mm3 (Volume = length*width2/2). These mice were sacrificed on day 16 to collect the tumors for the hypoxia staining and crucial organs for the hematoxylin & eosin (H&E) staining.

The tumor tissues were removed for the frozen section. The sections were incubated overnight with an anti-pimonidazole mouse monoclonal antibody (100 times dilution, Hypoxyprobe Inc.). Then, an Alexa Fluo 488 conjugated goat-anti-mouse antibody (100 times dilution, Jackson Inc.) was used as the secondary antibody to combine with the primary antibody. All sections were analyzed and imaged by CLSM (OLYMPUS).

Results and Discussion

Synthesis and Characterization

The synthesis procedures are shown in Scheme 1. The Au-Pt NPs were synthesized through a co-reduction of H2PtCl6 and HAuCl4 by L-ascorbic acid as a chelating agent to slow down the kinetics of the reduction reaction in a one-pot method. To improve the biocompatibility of the Au-Pt NPs, polyethylene glycol (maleic anhydridealt-1-octadecene) (C18-PMH-PEG5k) was used to modify it via stacking. According to the TEM mages (Figure 1A), the Au-Pt NPs were uniformly dispersed and formed spherical aggregations with a diameter of about 150 ± 20 nm. The ultraviolet absorption spectrum showed that there was no characteristic peak of Au-Pt NPs (Figure S1). The energy-dispersive spectroscopy (EDS) elemental mapping images (Figure 1B) showed that the Au and Pt atoms were uniformly distributed in the spherical aggregations. Au and Pt as high atomic number elements, would absorb, scatter, and emit radiation energy to enhance the radiation dose deposition at the interface of the surrounding tissue.35 The prepared Au-Pt NPs maintained uniform dispersion and good stability in 10% fetal bovine serum (FBS), which indicated potential for its biological application (Figure 1C and E). The Zeta potential of Au-Pt (−18.9 mV) and Au-Pt NPs (−21.1 mV) were similar (Figure 1D).

Scheme 1 Schematic illustrations for the fabrication of Au-Pt NPs and synergistic radiotherapy by employing tumor microenvironment.

Figure 1 The schematic procedure and characterization of Au-Pt NPs. (A) TEM image, (B) the high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) and elemental mapping images, (C) Hydrodynamic diameters of Au-Pt NPs in 10% FBS and PBS measured by DLS, (D) Zeta potential of Au-Pt NPs, (E) Hydrodynamic diameters of Au-Pt NPs 10% FBS and PBS at different times, (F) Oxygen generation in H2O2 solution (3.2 mM) with different concentrations of Au-Pt NPs at pH 6.75.

More importantly, we found that Au-Pt NPs catalyzed the reaction of H2O2 to O2. After different concentrations of Au-Pt were added to H2O2 solutions (pH 6.75) the change in the oxygen concentration was measured using a portable dissolved oxygen meter. The oxygen content did not change in the presence of only H2O2. However, the oxygen production rate increased gradually with an increase in the concentration of Au-Pt, which indicated the excellent CAT-like activity of Au-Pt NPs (Figures 1F and S2). Excessive reactive O2 species (such as H2O2 derived by cancer cells) is one of the oxidative stresses within the tumor microenvironment. The triggering off hypoxia stimulates autophagy and glycolysis through HIF1α and NFκB signaling, which promotes tumor growth and metastasis.3,36 Increasing the decomposition of H2O2 in TME by various nanomaterials would increase the therapeutic effect of treating tumors with phototherapy, chemodynamic therapy, and radiotherapy.37,38

In vitro Enhanced Radiotherapy

According to the MTT assay, the Au-Pt NPs exhibited negligible toxicity to human umbilical endothelial vein cells (HUEVC) and 4T1 cells at different concentrations of Au-Pt NPs at 24 h after treatment (Figure 2A). Furthermore, X-Rays alone (0–4 Gy) also exhibited limited toxicity to HUEVC cells and 4T1 cells (Figure 2B). On the other hand, the results showed that cells cultured without Au-Pt NPs exhibited excellent viability after irradiation with X-rays. The MTT assay revealed that Au-Pt NPs are an excellent radiosensitizer for X-ray-triggered in vitro cancer RT (Figure 2C). The relative cell viability of the 4T1 cells after irradiation and 24 h after treatment with Au-Pt NPs decreased greatly compared to X-Ray treatment alone. When combined with Au-Pt NPs treatment, the relative cell viability of groups irradiated with X-rays (4 Gy) decreased to 45% (with 100μg/mL Au-Pt NPs) and 22% (with 200μg/mL Au-Pt NPs). The colony formation assay revealed that at the same X-ray irradiation intensity, the clone formation numbers were reduced in the presence of Au-Pt NPs, which demonstrated its enhanced antigrowth effects (Figure 2D). The double-strand DNA breaks were evaluated by γ-H2AX staining because these breaks are considered to be the major cause of X-ray induced cell death.39 Low signals of the γ-H2AX foci were detected for cells incubated with PBS and Au-Pt NPs alone. In contrast, a higher level of DNA damage was observed for cells irradiated with X-rays. However, cells irradiated with X-rays and treated with Au-Pt NPs appeared to have a higher level of DNA damage, which was further evidencing of the radio-sensitizing function of our nanoparticles (Figure 2E). All of these assays indicated that the cooperation of Au-Pt NPs and irradiation with X-rays can inhibit the proliferation of cancer cells.

Figure 2 Relative cell viability of HUEVC cells and 4T1 cells treated with Au-Pt NPs (A) and irradiation (B) for 24 h. (C) Relative cell viability of 4T1 cells after irradiation for 24 h treated with Au-Pt NPs. (D) Clonogenic cell survival curve was generated for 4T1 cells. (E) Representative immunofluorescence images of phosphorylated H2AX (γH2AX) in 4T1 cells after irradiation for 24 h treated with Au-Pt NPs.

Furthermore, the pathways of cell death were assessed using live/dead dye and the Annexin V-FITC Apoptosis Detection Kit. The 4T1 cells were stained with live/dead dye as described in the surface marker staining protocol above. The signals of the PI (red) showed a dramatic increase in tumors injected with Au-Pt NPs and irradiated with X-rays compared to the tumors treated with FBS and Au-Pt NPs alone (Figure 3A). A flow cytometry-based apoptosis assay was performed to determine whether there is synergy between the Au-Pt NPs and X-rays in affecting apoptosis. The apoptosis/necrosis of the 4T1 cells treated with PBS, and X-rays were about 9.12% and 25%, respectively. The apoptosis/necrosis of the combination therapy group was more than 37%. Our results showed that Au-Pt NPs significantly affect apoptosis of 4T1 cells treated with X-rays compared with the control groups (Figure 3B and C).

Figure 3 (A) LIVE/DEAD staining of 4T1 cells by staining with FDA (green) and PI (red) after different treatments (scale bar: 200 μm). (B, C) Flow cytometric analysis of the apoptosis of 4T1 cells by staining with Annexin V-FITC and PI after different treatments (*P < 0.01).

Pharmacokinetics and Biodistribution

At different points in time post the intravenous injection (i.v.) of Au-Pt NPs, mouse blood samples were collected and the radioactive counts measured (Figure 4A). The nanoparticles were demonstrated to have a long blood circulation half-life (t1/2 = 0.5 h). The ICP-MS signals were observed in many organs, especially in the liver of mice, because of the clearance of the nanoparticles by the reticuloendothelial system (RES) (Figure 4B). The tumor uptake of the Au-Pt NPs was determined to be 6.5% ID/g at 24 h post injection. We used CT imaging to study the in vivo behaviors of the Au-Pt NPs because they exhibited the ability to be detected with CT fluorescence imaging (Figure S3). Mice bearing 4T1 tumors were thus injected intravenously with Au-Pt NPs, then imaged with a CT imaging system. The time-dependent increase of the CT signals (Figure 4C) was observed in the tumor after the intravenous injection with Au-Pt NPs, which indicated the efficient uptake of Au-Pt NPs by the tumor because of the EPR effect.

Figure 4 (A) Inductively Coupled Plasma Optical Emission Spectrometer (ICP-OES) analysis of Au-Pt NPs after tail intravenous injection for different times. (B) Organ biodistribution according to ICP-OES signal (N = 3 animals) with Au-Pt NPs. Data represent mean ± s.d. (C) The thermal images of 4T1 tumor bearing mice with injection of Au-Pt NPs for different times.

In vivo Enhanced Radiotherapy

Since catalase has the ability to decompose H2O2 to H2O and O2, we assessed the ability of Au-Pt NPs to reduce tumor hypoxia in vivo using an immunofluorescent staining assay (Figure 5A). Four h post injection of different nanoparticles, BALB/c mice bearing CT26 tumors were sacrificed and their tumors were collected for immunofluorescence staining. The signals of the hypoxia-probe (pimonidazole) showed a dramatic decrease in tumors injected with Au-Pt NPs because of the decomposition of H2O2 that generated O2 in the tumor microenvironment by the catalase loaded inside the nanoparticles. By contrast, similar to the untreated tumors, tumors from mice treated with X-rays only exhibited large hypoxic areas.

Figure 5 (A) Representative immunofluorescence images of tumor slices after hypoxia staining (scale bar: 100 μm). The hypoxia areas were stained by anti-pimonidazole antibody (green, FITC). (B) Relative tumor volume after various treatments indicated. (C) Tumor weight of sacrificed mice at Day 16 (*P< 0.01). (D) Change curves for the body weight of mice. (E) H&E staining of tumor tissues at Day 16 (scale bar: 100 μm).

Inspired by the eminent lethality of cancer cells in vitro because of the Au-Pt NPs, the therapeutic efficacy on tumor-bearing mice was then studied. The 4T1 tumor-bearing BALB/c mice were randomly allocated to four groups: (a) control group (PBS); (b) Au-Pt NPs; (c) X-ray (8Gy); (d) Au-Pt NPs + X-ray. When sacrificed on day 16, the tumors of the mice from the four groups demonstrated that the size of the tumors in the mice treated with Au-Pt NPs was smaller than in any of the other groups (Figure S4). Compared to X-ray treatment alone which resulted in only partly delayed tumor growth (Tumor volume: 459.5±76.09 mm3, Tumor weight: 0.3065±0.049 g), treatment with Au-Pt NPs, at the same level of irradiation with X-rays, resulted in about a twofold increase in the inhibitory effect on the growth of the tumor (Tumor volume: 231.7±63.35 mm3, Tumor weight: 0.1662±0.032 g) (Figure 5B and C). In addition, the mice treated with Au-Pt NPs exhibited no loss of body weight, which indicated that there were almost no short-term side effects (Figure 5D). Moreover, the H&E staining of the main organs from the mice showed no pathological change, which indicated that there was no poisoning of the organisms (Figure S5). In addition, the H&E staining was conducted to investigate any morphological changes and apoptosis of the cancer cells in the different treatment groups. As illustrated in Figure 5E, we found that a large number of morphological changes and apoptosis of the cancer cells were dispersed throughout the whole tumor tissue from mice treated with Au-Pt NPs (Figure 5E). Taken together, the Au-Pt NPs amplified the killing effect of X-rays, which lead to the effective suppression of tumor growth without any distinct damage to surrounding non-tumor tissues.


In summary, we developed Au-Pt NPs via a simple method that simultaneously possesses metal nanoparticle mediated radio-sensitization, and enzyme catalytic activities. A general mechanism in nanoparticle-based radiotherapy was uncovered in that heavy metal NPs possesses a high X-ray photon capture cross-section and Compton scattering effect which escalated the damage of DNA in tumor cells. Furthermore, our Au-Pt NPs increased the decomposition of H2O2 in TME and improved the anoxic status of the tumors treated with X-rays and enhanced the efficacy of radiotherapy. More importantly, in vitro, and in vivo data showed that Au-Pt NPs could effectively inhibit tumor growth with no significant side effects on normal tissues and organs. Therefore, our work developed a low toxicity novel radiosensitizer for enhanced tumor radiotherapy via attenuation of hypoxia. All completed clinical trials have demonstrated the safety of gold-based nanomaterials.40 In a recent clinical trial, gold-silica nanoshells (GSNs) were designed and used for ablating prostate tumors in patients without any obvious treatment-related side effects.41 Our findings further highlight the great potential application of Au-Pt NPs in the future clinical treatment of cancers.


This work was supported by the Foundation of Jiangsu Provincial Medical Innovation Team (Grant NO. CXTDA 2017042) and the Scientific Research Program of the Jiangsu Provincial Health and Family Planning Commission (H2017076).


The authors declare no competing interests.


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