State Key Laboratory on Integrated Optoelectronics, College of Electronic Science and Engineering, Jilin University, 2699 Qianjin Street, Changchun, 130012, P. R. China.
Department of Cell Biology, College of Basic Medical Sciences, Jilin University, Changchun, Jilin 130021, P. R. China.
J Mater Chem B. 2019 Oct 14;7(38):5797-5807. doi: 10.1039/c9tb01346f. Epub 2019 Sep 4.
Photodynamic therapy (PDT), as an essential tumor treatment method, has received great attention; however, there are still some challenges such as hydrophobicity of most of the photosensitizers, safety of in vivo transport, and characteristics of oxygen consumption. Herein, we used albumin as the nanocarrier for the loading of Chlorin e6 (Ce6) photosensitizer. In the meantime, tirapazaming (TPZ) was co-loaded onto the nanocomposite, which could be activated by hypoxia caused by PDT for enhanced therapy. Considering the over irradiation problem, a strategy for measuring PDT degree by ratio fluorescence was utilized. The PDT monitoring design relies on ratio emissions of C6 (Coumarin 6) and Ce6 molecules since the red emission of Ce6 is dependent on the PDT capability. Based on the characterization of the albumin nanocomposites, we further explored the combined therapy effect at both the in vitro and in vivo levels and attained the corresponding results.
光动力疗法(PDT)作为一种重要的肿瘤治疗方法,受到了广泛关注;然而,它仍然存在一些挑战,如大多数光敏剂的疏水性、体内运输的安全性以及耗氧量的特点。在这里,我们使用白蛋白作为纳米载体来负载氯乙酮(Ce6)光敏剂。同时,将替拉扎明(TPZ)共载于纳米复合物上,该复合物可被 PDT 引起的缺氧激活,以增强治疗效果。考虑到过度照射的问题,我们采用了一种通过比率荧光测量 PDT 程度的策略。PDT 监测设计依赖于 C6(香豆素 6)和 Ce6 分子的比率发射,因为 Ce6 的红色发射取决于 PDT 的能力。基于白蛋白纳米复合材料的表征,我们进一步在体外和体内水平上探索了联合治疗效果,并获得了相应的结果。