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Proton-Driven Transformable 1 O2 -Nanotrap for Dark and Hypoxia Tolerant Photodynamic Therapy.


ABSTRACT: Despite the clinical potential, photodynamic therapy (PDT) relying on singlet oxygen (1 O2 ) generation is severely limited by tumor hypoxia and endosomal entrapment. Herein, a proton-driven transformable 1 O2 -nanotrap (ANBDP NPs) with endosomal escape capability is presented to improve hypoxic tumor PDT. In the acidic endosomal environment, the protonated 1 O2 -nanotrap ruptures endosomal membranes via a "proton-sponge" like effect and undergoes a drastic morphology-and-size change from nanocubes (≈94.1 nm in length) to nanospheres (≈12.3 nm in diameter). Simultaneously, anthracenyl boron dipyrromethene-derived photosensitizer (ANBDP) in nanospheres transforms to its protonated form (ANBDPH) and switches off its charge-transfer state to achieve amplified 1 O2 photogeneration capability. Upon 730 nm photoirradiation, ANBDPH prominently produces 1 O2 and traps generated-1 O2 in the anthracene group to form endoperoxide (ANOBDPH). Benefitting from the hypoxia-tolerant 1 O2 -release property of ANOBDPH in the dark, the 1 O2 -nanotrap brings about sustained therapeutic effect without further continuous irradiation, thereby achieving remarkable antitumor performance.

SUBMITTER: Chen D 

PROVIDER: S-EPMC9189669 | biostudies-literature | 2022 Jun

REPOSITORIES: biostudies-literature

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Proton-Driven Transformable <sup>1</sup> O<sub>2</sub> -Nanotrap for Dark and Hypoxia Tolerant Photodynamic Therapy.

Chen Dapeng D   Dai Hanming H   Wang Weili W   Cai Yu Y   Mou Xiaozhou X   Zou Jianhua J   Shao Jinjun J   Mao Zhengwei Z   Zhong Liping L   Dong Xiaochen X   Zhao Yongxiang Y  

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20220418 17


Despite the clinical potential, photodynamic therapy (PDT) relying on singlet oxygen (<sup>1</sup> O<sub>2</sub> ) generation is severely limited by tumor hypoxia and endosomal entrapment. Herein, a proton-driven transformable <sup>1</sup> O<sub>2</sub> -nanotrap (ANBDP NPs) with endosomal escape capability is presented to improve hypoxic tumor PDT. In the acidic endosomal environment, the protonated <sup>1</sup> O<sub>2</sub> -nanotrap ruptures endosomal membranes via a "proton-sponge" like eff  ...[more]

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