Department of Ultrasound, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310000, China.
Department of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
J Mater Chem B. 2020 Oct 21;8(40):9251-9257. doi: 10.1039/d0tb01357a.
The major limitations of photodynamic therapy (PDT) are the poor tissue penetration of excitation light and the neutralization of reactive oxygen species (ROS) generated by overexpressed glutathione (GSH) in cancer cells. Despite tremendous efforts to design nanoplatforms, PDT still suffers from unsatisfactory effects. Furthermore, the residual of nanomaterials in the body has restricted their clinical application. To address these issues, Janus nanocomposites containing an Yb/Er codoped NaYF4 upconverting nanocrystal head and a disulfide-bridged mesoporous organosilicon body (UCN/MON) with loaded chlorin e6 (Ce6) were designed. On one hand, the upconverting nanocrystal head can convert near-infrared (NIR) light into visible light to activate Ce6 to release ROS. On the other hand, the silica body can be degraded though a redox reaction with GSH, to not only improve the tumor selectivity of the photosensitizer by redox- and pH-triggered Ce6 release, but also diminish the concentration of GSH in cancer cells to reduce the depletion of ROS. Thereby, an enhanced PDT triggered by NIR irradiation was achieved. Furthermore, UCN/MONs showed a higher clearance rate after therapeutic actions than nonbiodegradable UCN/MSNs due to their biocompatibility. Taken together, this work revealed the potential of UCN/MONs for highly efficient and NIR-induced PDT, highlighting the prospects of UCN/MONs in the clinic.
光动力疗法 (PDT) 的主要局限性是激发光的组织穿透性差,以及癌细胞中过表达的谷胱甘肽 (GSH) 中和生成的活性氧物种 (ROS)。尽管在设计纳米平台方面付出了巨大努力,但 PDT 的效果仍然不尽如人意。此外,纳米材料在体内的残留限制了它们的临床应用。为了解决这些问题,设计了含有 Yb/Er 共掺杂 NaYF4 上转换纳米晶头和负载有叶绿素 e6 (Ce6) 的二硫键桥联介孔有机硅体 (UCN/MON) 的 Janus 纳米复合材料。一方面,上转换纳米晶头可以将近红外 (NIR) 光转换为可见光以激活 Ce6 释放 ROS。另一方面,硅酮体可以通过与 GSH 的氧化还原反应降解,不仅通过氧化还原和 pH 触发的 Ce6 释放提高光敏剂的肿瘤选择性,还可以减少癌细胞中 GSH 的浓度以减少 ROS 的消耗。从而实现了由 NIR 照射引发的增强 PDT。此外,由于其生物相容性,UCN/MONs 在治疗作用后表现出比不可生物降解的 UCN/MSNs 更高的清除率。总之,这项工作揭示了 UCN/MONs 用于高效和近红外诱导 PDT 的潜力,突出了 UCN/MONs 在临床中的前景。