光热治疗
光动力疗法
光敏剂
胶体金
活性氧
纳米技术
纳米医学
肿瘤微环境
生物医学中的光声成像
化学
声动力疗法
纳米颗粒
癌症治疗
材料科学
医学
生物物理学
癌症
癌症研究
光化学
肿瘤细胞
生物化学
内科学
有机化学
物理
光学
生物
作者
Dongya Liu,Lingyan Liu,Feiyang Liu,Mengfan Zhang,Peng Wei,Tao Yi
标识
DOI:10.1002/advs.202100074
摘要
Tumor microenvironment-responsive nanodrugs offer promising opportunities for imaging-guided precision therapy with reduced side effects. Considering that the antitumor effect is closely related to the size of the nanodrugs, it is particularly important to develop a therapeutic system with size adjustability in the tumor microenvironment, which is still a great challenge in the field of nanotheranostics. Herein, a reactive oxygen species (ROS)-activated aggregation strategy is reported for imaging-guided precision therapy of tumors. The ROS-activated nanoplatform is constructed based on gold nanoparticles (AuNPs) coated with an HOCl probe on its surface (namely, Au-MB-PEG NPs). The Au-MB-PEG NPs show high sensitivity toward HOCl, resulting in the modulation of surface charge and rapid aggregation of AuNPs, and simultaneous release of methylene blue as a photosensitizer for photodynamic therapy (PDT). In the tumor environment, the aggregated AuNPs ensure higher tumor accumulation and retention. Furthermore, the redshift of the absorption of aggregated AuNPs leads to activated photoacoustic imaging signals and photothermal therapy (PTT) under near-infrared irradiation. Au-MB-PEG NPs thus efficiently inhibit the tumor growth through combined PTT-PDT therapy. This work contributes to the design of stimuli-induced size-aggregation nanodrugs, thereby attaining advanced performance in cancer diagnosis and treatment.
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