State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing, 210023, China.
Dr. Li Dak-Sum Research Centre, The University of Hong Kong-Karolinska Institutet Collaboration in Regenerative Medicine, The University of Hong Kong, Pokfulam, Hong Kong, China.
Biomaterials. 2019 Feb;192:179-188. doi: 10.1016/j.biomaterials.2018.10.018. Epub 2018 Oct 17.
Selecting the timing of laser treatment is an important task for improving O-dependent photodynamic therapy (PDT) efficiency. Here, a black phosphorus-based strategy was developed for dual-mode monitoring oxygen self-supply, enhancing photodynamic therapy, and feeding back therapeutic effect. The hybridized nanoplatform (R-MnO-FBP) was prepared by assembly of Rhodamine B (RhB)-encapsulated manganese dioxide (R-MnO) as O supplier and indicator, and fluorescein isothiocyanate (FITC)-labelled peptide-functionalized black phosphorus as the theranostic agent. The time-dependent assays suggested that the O release was proportional to the liberation of Mn and RhB in the R-MnO-FBP system. After specific delivery into cancer cells, R-MnO-FBP was dissociated in the acidic and HO-rich environment and generated oxygen to overcome hypoxia-associated PDT resistance. In the meantime, it released both Mnand RhB dye, leading to dual-mode (magnetic resonance imaging/fluorescence imaging) monitoring of the oxygen self-supply process. More significantly, the imaging-guided PDT in hypoxic cells displayed 51.6% of cell apoptosis at optimizing timing of laser application, which could also be confirmed by the FITC fluorescence recovery induced by the activated caspase-3 in apoptotic cells. In vivo photonic therapy by R-MnO-FBP further demonstrated the ability of R-MnO-FBP to choose the timing of laser application, providing an efficient approach for the enhancement of PDT process.
选择激光治疗的时机是提高氧依赖光动力疗法(PDT)效率的重要任务。在这里,开发了一种基于黑磷的策略,用于双重模式监测氧气自供应、增强光动力疗法和反馈治疗效果。通过将封装有罗丹明 B(RhB)的二氧化锰(R-MnO)作为氧源和指示剂,以及异硫氰酸荧光素(FITC)标记的肽功能化黑磷作为治疗剂进行组装,制备了杂交纳米平台(R-MnO-FBP)。时间依赖性测定表明,R-MnO-FBP 体系中的 O 释放与 Mn 和 RhB 的释放成正比。在特定递送到癌细胞后,R-MnO-FBP 在酸性和富含 HO 的环境中解离并产生氧气以克服与缺氧相关的 PDT 抵抗。同时,它释放了 Mn 和 RhB 染料,导致氧气自供应过程的双模(磁共振成像/荧光成像)监测。更重要的是,在优化激光应用时间的情况下,成像引导的缺氧细胞 PDT 显示出 51.6%的细胞凋亡,这也可以通过凋亡细胞中激活的 caspase-3 诱导的 FITC 荧光恢复来证实。R-MnO-FBP 的体内光疗进一步证明了 R-MnO-FBP 选择激光应用时间的能力,为增强 PDT 过程提供了一种有效的方法。