Yang Silan, Liu Yijun, Wu Tianyu, Zhang Xuan, Xu Shan, Pan Qingshan, Zhu Lianghui, Zheng Pengwu, Qiao Dan, Zhu Wufu
Jiangxi Provincial Key Laboratory of Drug Design and Evaluation, School of Pharmacy, Jiangxi Science & Technology Normal University, 605 Fenglin Rd., Nanchang, Jiangxi 330013, China.
Jiang Xi Institute for Drug Control, Jiangxi Provincial Drug Administration, 1566 Beijing East Road, Nanchang, Jiangxi 330029, China.
J Med Chem. 2025 Feb 13;68(3):3197-3211. doi: 10.1021/acs.jmedchem.4c02426. Epub 2025 Jan 9.
With the dilemma of limited efficacy of individual therapies, it is crucial to develop innovative combination therapy systems to target the complex pathogenesis of cancer. In this study, we designed a nanoprodrug ISL@MIL-101-ADT to facilitate synergistic delivery of hydrogen sulfide (HS) and prodrug ISL for specific eradication of tumor cells with minimal toxicity and maximal efficacy. The nanoprodrug passively targeted tumors through enhanced permeation and retention effects, followed by disintegration and release of IR780, lonidamine (LND), and HS. IR780 localizes LND to mitochondria to enhance therapeutic effects and turn on the phototherapy and chemotherapy when exposed to a laser; HS inhibits procancer signaling pathways and mitochondrial function. In vivo experiments have demonstrated that ISL@MIL-101-ADT exhibits excellent pharmacokinetic properties and significant tumor inhibitory effects. Additionally, this nanoprodrug possesses outstanding photothermal and fluorescence imaging capabilities. Therefore, we strongly believe that the nanoprodrug present herein holds great potential for application in cancer therapy.
鉴于单一疗法疗效有限的困境,开发创新的联合治疗系统以针对癌症的复杂发病机制至关重要。在本研究中,我们设计了一种纳米前药ISL@MIL-101-ADT,以促进硫化氢(HS)和前药ISL的协同递送,从而以最小的毒性和最大的疗效特异性根除肿瘤细胞。该纳米前药通过增强渗透和滞留效应被动靶向肿瘤,随后IR780、氯尼达明(LND)和HS分解并释放。IR780将LND定位于线粒体以增强治疗效果,并在暴露于激光时开启光疗和化疗;HS抑制促癌信号通路和线粒体功能。体内实验表明,ISL@MIL-101-ADT具有优异的药代动力学特性和显著的肿瘤抑制作用。此外,这种纳米前药具有出色的光热和荧光成像能力。因此,我们坚信本文所述的纳米前药在癌症治疗中具有巨大的应用潜力。