Li Xue, Zhang Xu, Guo Haizhen, Li Zhetao, Han Lei, Wang Sheng
School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
School of Life Sciences, Faculty of Medicine, Tianjin University, Tianjin 300072, China.
Colloids Surf B Biointerfaces. 2025 Sep;253:114775. doi: 10.1016/j.colsurfb.2025.114775. Epub 2025 May 11.
Photodynamic therapy (PDT), as a minimally invasive cancer therapy, demonstrates certain advantages in treating superficial tumors. However, it often faces challenges such as low reactive oxygen species (ROS) generation efficiency and non-targeted distribution of photosensitizers. The combination of chemotherapy and PDT can address the limitations of single modal therapies and improve therapeutic outcomes. In this work, we design a prodrug-based nanomedicine that can achieve photo-activated cascade drug release. Under 660 nm laser irradiation, the generated singlet oxygen can trigger the release of chemotherapeutic agent chlorambucil, cinnamaldehyde and quinone methyl. Chlorambucil can exert anti-tumor effects and cinnamaldehyde can increase intracellular hydrogen peroxide levels, while quinone methyl can consume intracellular glutathione. This process ultimately results in the amplification of ROS signals and further activation of prodrugs. This nanomedicine exhibits the ability to amplify oxidative stress and potent anticancer activity. In vivo experiments show that the nanomedicine can effectively inhibit tumor growth. This work provides a promising mutually beneficial strategy for achieving cooperative cancer therapy.
光动力疗法(PDT)作为一种微创癌症治疗方法,在治疗浅表肿瘤方面具有一定优势。然而,它常常面临诸如活性氧(ROS)生成效率低和光敏剂非靶向分布等挑战。化疗与光动力疗法相结合可以解决单一模式疗法的局限性并改善治疗效果。在这项工作中,我们设计了一种基于前药的纳米药物,它可以实现光激活级联药物释放。在660纳米激光照射下,产生的单线态氧可触发化疗药物苯丁酸氮芥、肉桂醛和醌甲基的释放。苯丁酸氮芥可发挥抗肿瘤作用,肉桂醛可增加细胞内过氧化氢水平,而醌甲基可消耗细胞内谷胱甘肽。这一过程最终导致ROS信号放大并进一步激活前药。这种纳米药物具有放大氧化应激和强大抗癌活性的能力。体内实验表明,该纳米药物可有效抑制肿瘤生长。这项工作为实现协同癌症治疗提供了一种有前景的互利策略。