Zhang Yafei, Bo Bingyang, Qin Jinglei, Liu Bei, Peng Hong-Shang
College of Science, Minzu University of China, Beijing 100081, People's Republic of China.
College of Science, Optical Science and Technology Laboratory, Department of Physics, Beijing Jiaotong University, Beijing 100044, People's Republic of China.
Nanotechnology. 2025 Feb 18;36(13). doi: 10.1088/1361-6528/adb437.
Zinc phthalocyanine (ZnPc), a promising second-generation photosensitizer, suffers from decreased quantum yield of singlet oxygen due to poor water solubility and prone-to-aggregation nature in both physiological environment and solid matrix. To address this issue, in this work we reported a simple ligand-assisted reprecipitation method to prepare aggregation-free ZnPc-doped nanoparticles (NPs). Specifically, a short-chain ligand hexylamine was introduced to coordinate with ZnPc during reprecipitation, so that to alleviate ZnPc aggregation in the polymeric nanomatrix. As a consequence, the as-prepared ZnPc-loaded NPs with an optimal loading content of 4 wt.% acquired a high singlet oxygen quantum yield (Φ) of 0.5, which was comparable to that of ZnPc monomer (Φ= 0.55). Moreover, 10 wt.% ZnPc-loaded NPs could still retain a singlet oxygen quantum yield of 0.38. Taking advantage of the aggregation-free nano-photosensitizers (NPSs), efficient photodynamic therapy effect was achieved on HeLa cells upon 660 nm photo-irradiation with an ultra-low light dose (1.8 J cm). This study not only presented a high efficient ZnPc-based NPS, but also proposed a new strategy to reduce the aggregation of metal complex in solid matrix through ligand coordination.
锌酞菁(ZnPc)作为一种很有前景的第二代光敏剂,由于其在生理环境和固体基质中水溶性差且易于聚集的特性,导致单线态氧的量子产率降低。为了解决这个问题,在本工作中,我们报道了一种简单的配体辅助再沉淀法来制备无聚集的ZnPc掺杂纳米颗粒(NPs)。具体而言,在再沉淀过程中引入短链配体己胺与ZnPc配位,从而减轻ZnPc在聚合物纳米基质中的聚集。结果,所制备的负载ZnPc的NPs,最佳负载量为4 wt.%,获得了0.5的高单线态氧量子产率(Φ),这与ZnPc单体的量子产率(Φ = 0.55)相当。此外,负载10 wt.% ZnPc的NPs仍可保持0.38的单线态氧量子产率。利用无聚集纳米光敏剂(NPSs),在660 nm光照射下,以超低光剂量(1.8 J/cm²)对HeLa细胞实现了高效的光动力治疗效果。本研究不仅展示了一种高效的基于ZnPc的NPS,还提出了一种通过配体配位减少固体基质中金属配合物聚集的新策略。