Liu Junwei, Liu Yang, Zhi Songsong, Yang Yonggang, Kim Heejeong, Wu Dapeng, Wang Ge, James Tony D, Yoon Juyoung, Zhang Hua
School of Chemistry and Chemical Engineering, Henan Normal University.
Henan International Joint Laboratory of Smart Molecules and Identification and Diagnostic Functions, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Xinxiang, Henan, 453007, P. R. China.
Angew Chem Int Ed Engl. 2025 Apr 17;64(17):e202425631. doi: 10.1002/anie.202425631. Epub 2025 Feb 26.
Single-mode photodynamic therapy (PDT) based on photochemical reactions is limited by the tumor microenvironment, which reduces the ablation efficiency for solid tumors. Making it vital to seek ways to improve the tumor therapeutic effect. Based on this, we propose a dual-mode intelligent nanotherapeutic system (HAP@BMPns) based on photochemical-biological effects. HAP@BMPns is composed of an acid-responsive high-calcium biomimetic nanomaterial (HAP) and photosensitizer (BMP), which can spontaneously activate photochemical (Type-I PDT) and biological effects for synergistic cancer therapy. HAP@BMPns breaks down upon entering tumor cells under acidic conditions, releasing a large amount of Ca and BMP. Triggering intracellular Ca overload, which induces mitochondrial damage, leading to apoptosis. Synchronously, Type-I PDT of BMP under two-photon (800 nm) laser irradiation becomes activated, resulting in enhanced destruction of tumor cells by the photochemical effect. Cell studies have indicated that HAP@BMPns (41.6 μg/mL) exhibits a strong inhibitory efficiency on tumor cells growth, with low (22.4 %) survival rate. However, the individual components, i. e. BMP (5.0 μM) and HAP (41.6 μg/mL) display low inhibitory efficiency with high survival rates (55.9 % and 63.0 % respectively). Therefore, this dual-mode synergistic treatment strategy using acid-triggered photochemical-biological effects significantly enhances the ablation of solid tumors, realizing the synergistic effect. We hope that this design strategy can provide guidance for the design and development of a tumor therapeutic platform.
基于光化学反应的单模光动力疗法(PDT)受到肿瘤微环境的限制,这降低了实体肿瘤的消融效率。因此,寻求提高肿瘤治疗效果的方法至关重要。基于此,我们提出了一种基于光化学-生物学效应的双模智能纳米治疗系统(HAP@BMPns)。HAP@BMPns由酸响应性高钙仿生纳米材料(HAP)和光敏剂(BMP)组成,可自发激活光化学(I型PDT)和生物学效应以协同治疗癌症。HAP@BMPns在酸性条件下进入肿瘤细胞后会分解,释放大量的钙和BMP。引发细胞内钙超载,诱导线粒体损伤,导致细胞凋亡。同时,在双光子(800 nm)激光照射下,BMP的I型PDT被激活,通过光化学效应增强对肿瘤细胞的破坏。细胞研究表明,HAP@BMPns(41.6 μg/mL)对肿瘤细胞生长具有很强的抑制效率,存活率低(22.4%)。然而,单个组分,即BMP(5.0 μM)和HAP(41.6 μg/mL)的抑制效率较低,存活率较高(分别为55.9%和63.0%)。因此,这种利用酸触发光化学-生物学效应的双模协同治疗策略显著增强了实体肿瘤的消融,实现了协同效应。我们希望这种设计策略能够为肿瘤治疗平台的设计和开发提供指导。