Pd@Au Bimetallic Nanoplates Decorated Mesoporous MnO <sub>2</sub> for Synergistic Nucleus‐Targeted NIR‐II Photothermal and Hypoxia‐Relieved Photodynamic Therapy

Yiyi Zhang(University of Science and Technology Beijing), Fan Lv(Peking University), Yaru Cheng(University of Science and Technology Beijing), Zhipeng Yuan(University of Science and Technology Beijing), Fan Yang(University of Science and Technology Beijing), Conghui Liu(University of Science and Technology Beijing), Yu Cao(University of Science and Technology Beijing), Kai Zhang(University of Science and Technology Beijing), Huiting Lu(University of Science and Technology Beijing), Shah Zada(University of Science and Technology Beijing), Shaojun Guo(Peking University), Haifeng Dong(University of Science and Technology Beijing), Xueji Zhang(University of Science and Technology Beijing)
Advanced Healthcare Materials
December 10, 2019
Cited by 101

Abstract

Abstract Bimetallic nanoparticles have received considerable attention owing to synergistic effect and their multifunctionality. Herein, new multifunctional Pd@Au bimetallic nanoplates decorated hollow mesoporous MnO 2 nanoplates (H‐MnO 2 ) are demonstrated for achieving not only nucleus‐targeted NIR‐II photothermal therapy (PTT), but also tumor microenvironment (TME) hypoxia relief enhanced photodynamic therapy (PDT). The Pd@Au nanoplates present a photothermal conversion efficiency (PTCE) as high as 56.9%, superior to those PTAs activated in the NIR‐II region such as Cu 9 S 5 nanoparticles (37%), Cu 3 BiS 3 nanorods (40.7%), and Au/Cu 2− x S nanocrystals (43.2%). They further functionalize with transactivator of transcription (TAT) moiety for cell nuclear‐targeting and biodegradable hollow mesoporous MnO 2 (≈100 nm) loaded with photosensitizer Ce6 (TAT‐Pd@Au/Ce6/PAH/H‐MnO 2 ) to construct a hierarchical targeting nanoplatform. The as‐made TAT‐Pd@Au/Ce6/PAH/H‐MnO 2 demonstrates good premature renal clearance escape ability and increased tumor tissue accumulation. It can be degraded in acidic TME and generate O 2 by reacting to endogenous H 2 O 2 to relieve the hypoxia for enhanced PDT, while the released small TAT‐Pd@Au nanoplates can effectively enter into the nucleus to mediate PTT. As a result, a remarkable therapeutic effect is achieved owing to the synergistic PTT/PDT therapy. This hierarchical targeting, TME‐responsive, cytoplasm hypoxia relief PDT, and nuclear NIR‐II PTT synergistic therapy can pave a new avenue for nanomaterials‐based cancer therapy.


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