Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, Sichuan University, Chengdu, 610064, P. R. China.
Small. 2023 Jun;19(23):e2300594. doi: 10.1002/smll.202300594. Epub 2023 Feb 8.
A primary concern about photodynamic therapy (PDT) is its inability to regulate the generation levels of reactive oxidative species (ROS) based on the complex microenvironment, resulting in the impairment toward normal tissues and immunosuppression. Besides, tumor metastasis also compromises PDT's efficacy and drives mortality. However, it is very challenging to achieve such two goals within one nanosystem. Here, the nanoassembly (CPR) with self-regulated photodynamic and antimetastasis properties comprises three parts: chlorin e6-conjugated β-cyclodextrin (CD-Ce6) acts as the main PDT agent and ferrocene (Fc)-terminated phenylboronic acid-containing conjugates entering into the cavity of CD-Ce6, as well as rosmarinic acid (RA)-boronic acid crosslinked shell. Compared with non-crosslinked counterpart, CPR displays better stability and enhanced tumor accumulation. Under laser irradiation, CPR generates plenty of ROS to damage tumor cells and induce immunogenic cell death. Mildly acidic TME partly cleaves the crosslinkers to dissociate antioxidant RAs from micelles, which together with Fc in CPR scavenge PDT-induced ROS in the TME. By contrast, under acidic lysosomal conditions, Fc catalyzes abundant H O in tumor cells to produce highly cytotoxic •OH, while RA continuously reduces ferroptosis-generated Fc into Fc, both to augment the PDT efficacy in tumor cells. CPR also remarkably hinders the epithelial-mesenchymal transition to prevent the lung metastasis.
光动力疗法(PDT)的一个主要关注点是其无法根据复杂的微环境调节活性氧(ROS)的产生水平,导致正常组织受损和免疫抑制。此外,肿瘤转移也会影响 PDT 的疗效并导致死亡率上升。然而,在一个纳米系统中实现这两个目标非常具有挑战性。在这里,具有自调节光动力和抗转移特性的纳米组装体(CPR)由三部分组成:氯 e6 键合的 β-环糊精(CD-Ce6)作为主要 PDT 剂,以及进入 CD-Ce6 空腔的末端为 ferrocene(Fc)的含苯硼酸的缀合物,以及迷迭香酸(RA)-硼酸交联壳。与非交联对应物相比,CPR 表现出更好的稳定性和增强的肿瘤积累。在激光照射下,CPR 会产生大量的 ROS 来破坏肿瘤细胞并诱导免疫原性细胞死亡。微酸性 TME 部分裂解交联剂,将抗氧化剂 RA 从胶束中分离出来,CPR 中的 Fc 与其中的 Fc 一起清除 TME 中 PDT 诱导的 ROS。相比之下,在酸性溶酶体条件下,Fc 催化大量 H2O2 在肿瘤细胞中产生高细胞毒性的•OH,而 RA 不断将铁死亡产生的 Fc 还原为 Fc,从而增强肿瘤细胞中的 PDT 疗效。CPR 还显著抑制上皮-间充质转化,以防止肺转移。