ACS Appl Bio Mater. 2022 Nov 21;5(11):5333-5346. doi: 10.1021/acsabm.2c00724. Epub 2022 Oct 26.
Photothermal/photodynamic therapies (PTT/PDT) are multimodal approaches employing near-infrared (NIR) light-responsive photosensitizers for cancer treatment. In the current study, IR-775, a hydrophobic photosensitizer, was used in combination with a polyphenols ()-rich ethyl acetate extract from to treat cancer. IR-775 dye and polyphenols were encapsulated in a poly(lactic acid) polymeric nanosystem (PIR NPs) to increase the cell bioavailability. The hydrodynamic diameter of PIR NPs is 142.6 ± 2 nm and exhibited physical stability. The nanosystem showed enhanced cellular uptake in a lung cancer cell line (A549). Cell cytotoxicity results indicate that PIR NPs showed more than 82.46 ± 3% cell death upon NIR light treatment compared to the control groups. Both PDT and PTT generate reactive oxygen species (ROS) and cause hyperthermia, thereby enhancing cancer cell death. Qualitative and quantitative analyses have depicted that PIR NPs with NIR light irradiation have decreased protein expression of HSP70 and PARP, and increased γ-H2AX, which collectively lead to cell death. After NIR light irradiation, the relative gene expression patterns of HSP70 and CDK2Na were also downregulated. Further, PIR NPs uptake has been studied in 3D cells and bioimaging in zebrafish models. In conclusion, the PIR NPs show good cancer cell cytotoxicity and present a potential nanosystem for bioimaging.
光热/光动力疗法(PTT/PDT)是一种多模态方法,采用近红外(NIR)光响应光敏剂治疗癌症。在本研究中,IR-775 是一种疏水性光敏剂,与 中富含多酚的乙酸乙酯提取物联合用于治疗癌症。IR-775 染料和多酚被包封在聚乳酸聚合物纳米系统(PIR NPs)中,以提高细胞的生物利用度。PIR NPs 的水动力学直径为 142.6±2nm,并表现出物理稳定性。该纳米系统在肺癌细胞系(A549)中表现出增强的细胞摄取。细胞毒性结果表明,与对照组相比,PIR NPs 在近红外光处理下表现出超过 82.46±3%的细胞死亡。PDT 和 PTT 都会产生活性氧(ROS)并导致过热,从而增强癌细胞死亡。定性和定量分析表明,PIR NPs 联合近红外光照射降低了 HSP70 和 PARP 的蛋白表达,并增加了 γ-H2AX,这共同导致细胞死亡。近红外光照射后,HSP70 和 CDK2Na 的相对基因表达模式也下调。此外,还研究了 PIR NPs 在 3D 细胞中的摄取和斑马鱼模型中的生物成像。总之,PIR NPs 表现出良好的癌细胞细胞毒性,并为生物成像提供了一种有潜力的纳米系统。