Laboratory of Veterinary Pathology and Nanopathology, College of Veterinary Medicine, China Agricultural University, Beijing, People's Republic of China.
China National Center for Food Safety Risk Assessment, Beijing, People's Republic of China.
Int J Nanomedicine. 2021 Jul 16;16:4863-4871. doi: 10.2147/IJN.S304713. eCollection 2021.
Phototherapy has significant potential as an effective treatment for cancer. However, the application of a multifunctional nanoplatform for photodynamic therapy (PDT) and photothermal therapy (PTT) at a single excitation wavelength remains a challenge.
The double emulsion solvent evaporation method was used to prepare toluidine blue@poly lactic-co-glycolic acid (TB@PLGA) nanoparticles (NPs). The biocompatibility of TB@PLGA NPs was evaluated, and a 660 nm luminescence was used as the light source. The photothermal effect, photothermal stability, and singlet oxygen yield of NPs in an aqueous solution verified the feasibility of NPs as a PTT/PDT synergistic therapy drug.
TB@PLGA NPs were successfully prepared and characterized. In vitro experiments demonstrated that TB@PLGA NPs can cause massive necrosis of tumor cells and induce apoptosis through a photodynamic mechanism under 660 nm laser irradiation. The TB@PLGA NPs also achieved optimal tumor inhibition effect in vivo.
The TB@PLGA NPs prepared in this study were applied as a dual-mode phototherapeutic agent under single laser irradiation. Both in vitro and in vivo experiments demonstrated the good potential of PTT/PDT for tumor inhibitors.
光疗在癌症治疗方面具有很大的潜力。然而,在单一激发波长下应用多功能纳米平台进行光动力疗法(PDT)和光热疗法(PTT)仍然是一个挑战。
采用双重乳液溶剂蒸发法制备甲苯胺蓝@聚乳酸-羟基乙酸共聚物(TB@PLGA)纳米粒子(NPs)。评估了 TB@PLGA NPs 的生物相容性,并使用 660nm 发光作为光源。验证了 NPs 在水溶液中作为 PTT/PDT 协同治疗药物的光热效应、光热稳定性和单线态氧产率。
成功制备并表征了 TB@PLGA NPs。体外实验表明,TB@PLGA NPs 在 660nm 激光照射下通过光动力机制可导致肿瘤细胞大量坏死并诱导细胞凋亡。TB@PLGA NPs 在体内也实现了最佳的肿瘤抑制效果。
本研究制备的 TB@PLGA NPs 可作为单激光照射下的双模式光疗剂。体外和体内实验均证明了 PTT/PDT 作为肿瘤抑制剂的良好潜力。