The Youth Innovation Team of Shaanxi Universities, Shaanxi Key Laboratory of Chemical Additives for Industry, College of Chemistry and Chemical Engineering, Shaanxi University of Science & Technology, Xi'an, 710021, China.
Key Laboratory of Emergency and Trauma, Ministry of Education, College of Emergency and Trauma, Hainan Medical University, Haikou, 571199, China.
Adv Sci (Weinh). 2023 Jun;10(16):e2207768. doi: 10.1002/advs.202207768. Epub 2023 Apr 7.
Targeting cancer cells with high specificity is one of the most essential yet challenging goals of tumor therapy. Because different surface receptors, transporters, and integrins are overexpressed specifically on tumor cells, using these tumor cell-specific properties to improve drug targeting efficacy holds particular promise. Targeted fluorescent prodrugs not only improve intracellular accumulation and bioavailability but also report their own localization and activation through real-time changes in fluorescence. In this review, efforts are highlighted to develop innovative targeted fluorescent prodrugs that efficiently accumulate in tumor cells in different organs, including lung cancer, liver cancer, cervical cancer, breast cancer, glioma, and colorectal cancer. The latest progress and advances in chemical design and synthetic considerations in fluorescence prodrug conjugates and how their therapeutic efficacy and fluorescence can be activated by tumor-specific stimuli are reviewed. Additionally, novel perspectives are provided on strategies behind engineered nanoparticle platforms self-assembled from targeted fluorescence prodrugs, and how fluorescence readouts can be used to monitor the position and action of the nanoparticle-mediated delivery of therapeutic agents in preclinical models. Finally, future opportunities for fluorescent prodrug-based strategies and solutions to the challenges of accelerating clinical translation for the treatment of organ-specific tumors are proposed.
以高特异性靶向癌细胞是肿瘤治疗中最重要但最具挑战性的目标之一。由于不同的表面受体、转运体和整合素在肿瘤细胞上特异性过表达,因此利用这些肿瘤细胞特异性特性来提高药物靶向效果具有特别的意义。靶向荧光前药不仅可以提高细胞内积累和生物利用度,还可以通过荧光的实时变化报告其自身的定位和激活。在这篇综述中,我们重点介绍了开发创新型靶向荧光前药的努力,这些前药可以在包括肺癌、肝癌、宫颈癌、乳腺癌、神经胶质瘤和结直肠癌在内的不同器官中的肿瘤细胞中高效积累。综述了荧光前药偶联物在化学设计和合成方面的最新进展和进展,以及如何通过肿瘤特异性刺激来激活它们的治疗效果和荧光,还提供了基于靶向荧光前药的工程纳米颗粒平台的策略背后的新视角,以及荧光读数如何用于监测临床前模型中治疗剂的纳米颗粒介导递送的位置和作用。最后,提出了基于荧光前药的策略的未来机遇和解决方案,以加速针对特定器官肿瘤的治疗的临床转化。