School of Chemical and Biomedical Engineering, Nanyang Technological University, Singapore, 637457, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, 636921, Singapore.
Angew Chem Int Ed Engl. 2022 Jun 27;61(26):e202202966. doi: 10.1002/anie.202202966. Epub 2022 Apr 27.
Activatable phototheranostics holds promise for precision cancer treatment owing to the "turn-on" signals and therapeutic effects. However, most activatable phototheranostic probes only possess photodynamic therapy (PDT) or photothermal therapy (PTT), which suffer from poor therapeutic efficacy due to deficient cellular oxygen and complex tumor microenvironment. We herein report a dual-locked activatable phototheranostic probe that activates near-infrared fluorescence (NIRF) signals in tumor, triggers PDT in response to a tumor-periphery biomarker, and switches from PDT to PTT upon detecting a tumor-core-hypoxia biomarker. This PDT-PTT auto-regulated probe exhibits complete tumor ablation under the photoirradiation of a single laser source by producing cytotoxic singlet oxygen at the tumor periphery and generating hyperthermia at tumor-core where is too hypoxic for PDT. This dual-locked probe represents a promising molecular design approach toward precise cancer phototheranostics.
由于“开启”信号和治疗效果,光激活治疗在精准癌症治疗方面具有广阔的前景。然而,大多数光激活光疗探针仅具有光动力疗法(PDT)或光热疗法(PTT),由于细胞氧含量不足和复杂的肿瘤微环境,其治疗效果较差。本文报道了一种双重锁定的光激活光疗探针,该探针可在肿瘤中激活近红外荧光(NIRF)信号,响应肿瘤周围的生物标志物触发 PDT,并在检测到肿瘤核心缺氧生物标志物时从 PDT 切换到 PTT。该 PDT-PTT 自动调节探针通过在肿瘤周围产生细胞毒性单线态氧,并在肿瘤核心产生过热(由于 PDT 缺氧而无法进行 PDT),在单一激光源的光照射下可完全消融肿瘤。这种双锁探针为精确的癌症光疗提供了一种很有前途的分子设计方法。