School of Medical Imaging, Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University, Tianjin, 300203, China.
College of Chemistry, Key Laboratory of Functional Polymer Materials (Ministry of Education) State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin, 300071, China.
Adv Sci (Weinh). 2024 Sep;11(36):e2404731. doi: 10.1002/advs.202404731. Epub 2024 Jul 28.
Real-time tracking of drug release from nanomedicine in vivo is crucial for optimizing its therapeutic efficacy in clinical settings, particularly in dosage control and determining the optimal therapeutic window. However, most current real-time tracking systems require a tedious synthesis and purification process. Herein, a supramolecular nano-tracker (SNT) capable of real-time tracking of drug release in vivo based on non-covalent host-guest interactions is presented. By integrating multiple cavities into a single nanoparticle, SNT achieves co-loading of drugs and probes while efficiently quenching the photophysical properties of the probe through host-guest complexation. Moreover, SNT is readily degraded under hypoxic tumor tissues, leading to the simultaneous release of drugs and probes and the fluorescence recovery of probes. With this spatial and temporal consistency in drug loading and fluorescence quenching, as well as drug release and fluorescence recovery, SNT successfully achieves real-time tracking of drug release in vivo (Pearson r = 0.9166, R = 0.8247). Furthermore, the released drugs can synergize effectively with fluorescent probes upon light irradiation, achieving potent chemo-photodynamic combination therapy in 4T1-bearing mice with a significantly improved survival rate (33%), providing a potential platform to significantly advance the development of nanomedicine and achieve optimal therapeutic effects in the clinic.
体内纳米药物释放的实时跟踪对于优化其临床治疗效果至关重要,特别是在剂量控制和确定最佳治疗窗口方面。然而,大多数当前的实时跟踪系统需要繁琐的合成和纯化过程。在此,提出了一种基于非共价主客体相互作用的超分子纳米追踪器(SNT),能够实时跟踪体内药物释放。通过将多个空腔集成到单个纳米颗粒中,SNT 实现了药物和探针的共装载,同时通过主客体络合有效地猝灭探针的光物理性质。此外,SNT 在缺氧肿瘤组织中容易降解,导致药物和探针同时释放,探针的荧光恢复。通过这种药物加载和荧光猝灭、药物释放和荧光恢复的时空一致性,SNT 成功实现了体内药物释放的实时跟踪(Pearson r = 0.9166,R = 0.8247)。此外,释放的药物在光照下可以与荧光探针有效协同,在携带 4T1 的小鼠中实现了强大的化学-光动力联合治疗,生存率显著提高(33%),为显著推进纳米医学的发展和在临床中实现最佳治疗效果提供了一个潜在的平台。