Tian Feng, Li Fengyan, Ren Linlin, Wang Qi, Jiang Chengfang, Zhang Yuqi, Li Mengmeng, Song Xinyue, Zhang Shusheng
Shandong Provincial Key Laboratory of Detection Technology for Tumor Markers, College of Medicine, Linyi University, Linyi 276005, PR China.
ACS Sens. 2022 Dec 23;7(12):3611-3633. doi: 10.1021/acssensors.2c02129. Epub 2022 Dec 1.
Acoustic-based imaging techniques, including ultrasonography and photoacoustic imaging, are powerful noninvasive approaches for tumor imaging owing to sound transmission facilitation, deep tissue penetration, and high spatiotemporal resolution. Usually, imaging modes were classified into "always-on" mode and "activatable" mode. Conventional "always-on" acoustic-based probes often have difficulty distinguishing lesion regions of interest from surrounding healthy tissues due to poor target-to-background signal ratios. As compared, activatable probes have attracted attention with improved sensitivity, which can boost or amplify imaging signals only in response to specific biomolecular recognition or interactions. The tumor microenvironment (TME) exhibits abnormal physiological conditions that can be used to identify tumor sections from normal tissues. Various types of organic dyes and biomaterials can react with TME, leading to obvious changes in their optical properties. The TME also affects the self-assembly or aggregation state of nanoparticles, which can be used to design activatable imaging probes. Moreover, acoustic-based imaging probes and therapeutic agents can be coencapsulated into one nanocarrier to develop nanotheranostic probes, achieving tumor imaging and cooperative therapy. Satisfactorily, ultrasound waves not only accelerate the release of encapsulated therapeutic agents but also activate therapeutic agents to exert or enhance their therapeutic performance. Meanwhile, various photoacoustic probes can convert photon energy into heat under irradiation, achieving photoacoustic imaging and cooperative photothermal therapy. In this review, we focus on the recently developed TME-triggered ultrasound and photoacoustic theranostic probes for precise tumor imaging and targeted tumor therapy.
基于声学的成像技术,包括超声检查和光声成像,由于其有助于声音传播、具有深层组织穿透能力以及高时空分辨率,是用于肿瘤成像的强大非侵入性方法。通常,成像模式分为“常开”模式和“可激活”模式。传统的基于声学的“常开”探头由于目标与背景信号比不佳,往往难以将感兴趣的病变区域与周围健康组织区分开来。相比之下,可激活探头因其灵敏度提高而受到关注,它能够仅在响应特定的生物分子识别或相互作用时增强或放大成像信号。肿瘤微环境(TME)呈现出异常的生理状况,可用于从正常组织中识别肿瘤切片。各种类型的有机染料和生物材料可与TME发生反应,导致其光学性质发生明显变化。TME还会影响纳米颗粒的自组装或聚集状态,可用于设计可激活的成像探头。此外,基于声学的成像探头和治疗剂可共同封装到一个纳米载体中,以开发纳米诊疗探头,实现肿瘤成像和协同治疗。令人满意的是,超声波不仅能加速封装治疗剂的释放,还能激活治疗剂以发挥或增强其治疗性能。同时,各种光声探头在照射下可将光子能量转化为热量,实现光声成像和协同光热治疗。在本综述中,我们重点关注最近开发的由TME触发的超声和光声诊疗探头,用于精确肿瘤成像和靶向肿瘤治疗。