School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, China.
J Mater Chem B. 2024 Jun 27;12(25):6175-6189. doi: 10.1039/d4tb00535j.
In this study, the heavy-atom-free BODIPY dendrimer TM-BDP was synthesized for near-infrared photodynamic therapy, and was composed of a triphenylamine-BODIPY dimer and four 1-(2-morpholinoethyl)-1-indole-3-ethenyl groups. The TM-BDP could achieve near-infrared photodynamic therapy through two different photosensitive pathways, which include one-photon excitation at 660 nm and two-photon excitation at 1000 nm. In the one-photon excitation pathway, the TM-BDP could generate singlet oxygen and superoxide radicals under 660 nm illumination. In addition, the one-photon PDT experiment in human nasopharyngeal carcinoma (CNE-2) cells also indicated that the TM-BDP could specifically accumulate in lysosomes and show great cell phototoxicity with an IC of 22.1 μM. In the two-photon excitation pathway, the two-photon absorption cross-section at 1030 nm of TM-BDP was determined to be 383 GM, which means that it could generate reactive oxygen species (ROS) under 1000 nm femtosecond laser excitation. Moreover, the two-photon PDT experiment in zebrafish also indicated the TM-BDP could be used for two-photon fluorescence imaging and two-photon induced ROS generation in biological environments. Furthermore, in terms of the ROS generation mechanism, the TM-BDP employed a novel spin-vibronic coupling intersystem crossing (SV-ISC) process for the mechanism of ROS generation and the femtosecond transient absorption spectra indicated that this novel SV-ISC mechanism was closely related to its charge transfer state lifetime. These above experiments of TM-BDP demonstrate that the dendrimer design is an effective strategy for constructing heavy-atom-free BODIPY photosensitizers in the near-infrared region and lay the foundation for two-photon photodynamic therapy in future clinical trials.
在这项研究中,合成了一种不含重原子的 BODIPY 树枝状大分子 TM-BDP,用于近红外光动力治疗,它由一个三苯胺-BODIPY 二聚体和四个 1-(2-吗啉乙基)-1-吲哚-3-乙烯基组成。TM-BDP 可以通过两种不同的光敏途径实现近红外光动力治疗,包括 660nm 的单光子激发和 1000nm 的双光子激发。在单光子激发途径中,TM-BDP 在 660nm 光照下可以产生单线态氧和超氧自由基。此外,人鼻咽癌细胞(CNE-2)的单光子 PDT 实验也表明,TM-BDP 可以特异性地在溶酶体中积累,并表现出很强的细胞光毒性,IC 为 22.1μM。在双光子激发途径中,TM-BDP 在 1030nm 处的双光子吸收截面被确定为 383GM,这意味着它可以在 1000nm 飞秒激光激发下产生活性氧物种(ROS)。此外,斑马鱼的双光子 PDT 实验也表明,TM-BDP 可以用于双光子荧光成像和双光子诱导生物环境中的 ROS 生成。此外,就 ROS 生成机制而言,TM-BDP 采用了一种新的自旋-振动耦合系间窜越(SV-ISC)过程来生成 ROS,飞秒瞬态吸收光谱表明,这种新的 SV-ISC 机制与它的电荷转移态寿命密切相关。TM-BDP 的这些实验表明,树枝状大分子设计是构建近红外区不含重原子的 BODIPY 光动力治疗剂的有效策略,为未来临床双光子光动力治疗奠定了基础。