Multi-targeted reactive oxygen species burst for cancer therapy
After polydopamine (PDA) and cancer cell membrane (M) coating, As/AsxOy@PDA@M nanosheets achieve active tumor targeting, long-term blood circulation, and smart theranostics through ·O2− and 1O2 production, glutathione consumption, and anti-oxidants inactivation to cut off “retreat routes” of ROS.
The modulation of intracellular reactive oxygen species (ROS) levels is crucial for cellular homeostasis and determination of cellular fate. A sublethal level of ROS sustains cell proliferation, differentiation and promotes tumor metastasis, while a drastic ROS burst directly induces apoptosis. Herein, surface-oxidized arsenene nanosheets (As/AsxOy NSs) with type II heterojunction are fabricated with efficient ·O2− and 1O2 production and glutathione consumption through prolonging the lifetime of photo-excited electron-hole pairs. Moreover, the portion of AsxOy with oxygen vacancies not only catalyzes a Fenton-like reaction, generating ·OH and O2 from H2O2 but also inactivates main anti-oxidants to cut off the “retreat routes” of ROS. After polydopamine (PDA) and cancer cell membrane (M) coating, the engineered As/AsxOy@PDA@M NSs serve as an intelligent theranostic platform with active tumor targeting and long-term blood circulation. Given its narrow-band-gap-enabled in vivo fluorescence imaging properties, As/AsxOy@PDA@M NSs could be applied as an imaging-guided non-invasive and real-time nanomedicine for cancer therapy.
Fig. 1: Schematic illustration of preparation and dual-modal imaging-guided cancer theranostics using As/AsxOy@PDA@M NSs.
Reactive oxygen species (ROS) are a group of highly reactive small molecules generated by all aerobic organisms, which include hydroxyl radicals (·OH), superoxide (·O2−), and other nonradical members such as hydrogen peroxide (H2O2) and singlet oxygen (1O2)1,2. In particular, the redox balance of ROS between oxidizing and reducing species, through the cooperation of various enzymes (e.g., catalase, glutathione peroxidase and superoxide dismutase), is important in cell growth, proliferation, and signaling pathways3,4,5,6. However, the overproduction of ROS can cause oxidative stress, leading to cellular damage as well as the subsequent functional decline of organ systems7.
Fig. 2: Morphology and composition characterization of ultrathin 2D As/AsxOy@PDA@M NSs.
Although cancer cells are under higher oxidative stress because of the disrupted ROS homeostasis, they have adapted themselves to the overproduced ROS by activating antioxidant systems (e.g., the upregulation of glutathione, GSH)4,8. Ironically, they can utilize ROS to drive other events required for tumor development1,3. Hence, the modulation of intracellular ROS levels is crucial for tumor cellular homeostasis and determination of cellular fate, as different concentrations and durations of ROS stress can induce distinct biological responses. Therefore, only a powerful ROS burst to induce a high ROS level can cause effective cellular damage and apoptotic cell death.
Fig. 3: Chemical composition and structure characterization of ultrathin 2D As/AsxOy@PDA@M NSs.
Herein, we designed and fabricated a type II heterojunction photocatalyst based on arsenene, which is capable of multiple independently targeted ROS bursts but requiring a low-dose administration and less excitation energy. As shown in Fig. 1, by coupling ball-grinding with probe sonication-based liquid exfoliating processes, arsenene nanosheets with partial surface oxidation of As (As/AsxOyNSs) constructed type II heterojunction were synthesized. The photo-excited electrons in the conduction band (CB) of As can be transferred to the CB of AsxOyto catalyze the generation of ·O2−from O2, while the holes in the valence band (VB) of AsxOycan be transferred to the VB of As to promote the oxidation of GSH. This type II heterojunction structure retards recombination of photogenerated electron–hole pairs of As/AsxOyNSs, which provides maximal power to catalyze the generation of ROS from O2on the one hand, while blocking the consumption of ROS by GSH on the other hand. Additionally, the As in As/AsxOyNSs could generate1O2through energy conversion, and the AsxOyin As/AsxOyNSs could inactivate some main anti-oxidants and anti-oxidases containing sulfhydryl groups to cut off the “retreat routes” of ROS. Moreover, the oxygen vacancies in As/AsxOyNSs not only catalyze the disproportionate reaction of H2O2via the high reduction ability of AsIII, but also generate O2through H2O2oxidation via the high oxidation capability of AsV. Hence, the prepared As/AsxOyNSs can mediate synergetic tripartite ROS generation and block two main ROS consumption pathways, producing a dramatic ROS burst. In addition, its efficient photothermal conversion ability under 808 nm laser irradiation alongside its intrinsic fluorescence properties further enriched the biomedical applications of As/AsxOyNSs. With the aid of surface engineering using polydopamine (PDA) and cancer cell membrane (M) coating, the obtained As/AsxOy@PDA@M NSs possess the advantages of a long blood circulation time, active cancer cell targeting, and tumor micro-environment (TME) responsive degradation, constituting excellent potential for in vivo fluorescence imaging-guided non-invasive and real-time cancer therapy.
Fig. 4: Fenton-like reaction-catalyzed ability of As/AsxOyNSs.
In line of the revealed complete elimination of tumors without recurrence, our work presents arsenene-based nanomedicine with multiple independently targeted ROS bursts for effective cancer therapy. We also anticipate the appearance of such heterojunction photocatalysts will be attractive in other settings beyond biomedical applications.
Fig. 5: Photocatalytic performance of As/AsxOyNSs.Fig. 6: Photothermal conversion and stability of As/AsxOy@PDA NSs.Fig. 7: Intracellular uptake and ROS generation.Fig. 8: Biocompatibility and cytotoxicity of As/AsxOy@PDA@M NSs.Fig. 9: In vivo imaging and anti-tumor performance of As/AsxOy@PDA@M NSs.
Fig. 10: Biocompatibility evaluation of As/AsxOy@PDA@M NSs.In conclusion, our work presents a means of creating a nanomedicine based on 2D As/AsxOy@PDA@M NSs capable of multiple independently targeted ROS bursts and a powerful capacity for tumor inhibition. The AsxOy indirectly induces the accumulation of intracellular ROS content by inactivating some main anti-oxidants and anti-oxidases to cut off the “retreat routes” of ROS. As acted as an efficient photosensitizer to catalyze the generation of 1O2 from O2 when exposed to the 660 nm laser, directly improving the intracellular ROS content. According to the band structure of As and AsxOy, a promising Type II heterojunction was formed. Thus, the electrons in the CB of As preferred to transfer to the CB of AsxOy. At the same time, the holes in the VB of AsxOy preferred to transfer to the VB of As, contributing to thoroughly separate photo-excited charges in the CB and VB of two different photosensitizers, further catalyzing the reduction of O2 to generate ·O2− and oxidation of GSH to inhibit the antioxidant ability of cancer cells. As a consequence, the efficient photo-excited charge separation in the As/AsxOy NSs-based Type II heterojunction can enhance the intracellular ROS content in both direct and indirect ways. The abundant oxygen vacancies on the surface of As/AsxOy NSs can catalyze a Fenton-like reaction to generate ·OH and O2 from H2O2, which can not only directly promote ROS burst but also essentially enhance the PDT effect. Additionally, after surface engineering with PDA and M shells, the produced As/AsxOy@PDA@M NSs not only possess remarkable biocompatibility with no long-term safety concerns in vivo, but also enhance the accumulation in tumors with homologous targeting ability to mediate high photothermal conversion efficiency under laser irradiation. The inherent outstanding fluorescence imaging ability of As/AsxOy@PDA@M NSs further demonstrate the imaging-guided therapeutic performance both in vitro and in vivo. Therefore, such an unprecedented type II heterojunction successfully induces a ROS burst in cancer cells and integrates imaging-guided chemo/photothermal/photodynamic therapies, establishing a paradigm for cancer therapy with high efficacy therapeutic efficacy and high biocompatibility.
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1. G Zheng, Q Gao, Y Jiang, L Lu, J Li,X Zhang, H Zhao, P Fan, Y Cui, F Gu, Y Wang. Instrumentation-compact digital microfluidic (DMF) reaction interface extended loop-mediated isothermal amplification (LAMP) for sample-to-answer testing of Vibrio parahaemolyticus. Analytical Chemistry, 2021, 93, 28, 9728–9736.
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R Yang, Z Gong, X Zhang, L Que. Single-walled carbon nanotubes (SWCNTs) and poly(3,4- ethylenedioxythiophene) nanocomposite microwire-based electronic biosensor fabricated by microlithography and layer-by-layer nanoassembly. Journal of Nanoscience and Nanotechnology, 2019,19(12), 7591-7595. https://doi.org/10.1166/jnn.2019.16752
Dr. Xingcai Zhang, Harvard/MIT Research Fellow; Science Writer/Editorial (Advisory) Board Member for Springer Nature, Elsevier, Materials Today, Royal Society of Chemistry, Wiley; Nature Nano Ambassador with 5 STEM degrees/strong background in sustainable Nature-derived/inspired/mimetic materials for biomed/sensing/catalysis/energy/environment applications, with more than 100 high-impact journal publications in Nature Reviews Materials (featured cover paper), etc.https://scholar.google.com/citations?hl=en&user=2vDraMoAAAAJ&view_op=list_works&sortby=pubdate
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