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用于癌症近红外二区光声成像和光免疫治疗的醌型半导体纳米颗粒

Quinoidal Semiconductor Nanoparticles for NIR-II Photoacoustic Imaging and Photoimmunotherapy of Cancer.

作者信息

Niu Gaoli, Song Guangkun, Kang Yong, Zhai Yanhong, Fan Yueyue, Ye Jiamin, Li Ruiyan, Li Runtan, Zhang Yanwei, Wang Hong, Chen Yongsheng, Ji Xiaoyuan

机构信息

Academy of Medical Engineering and Translational Medicine, Medical College, Tianjin University, Tianjin, 300072, China.

The First Affiliated Hospital of Henan Polytechnic University, Jiaozuo, 454000, China.

出版信息

Adv Mater. 2025 Feb;37(6):e2415189. doi: 10.1002/adma.202415189. Epub 2024 Dec 18.

Abstract

Photoagents with ultra-high near-infrared II (NIR-II) light energy conversion efficiency hold great promise in tumor phototherapy due to their ability to penetrate deeper tissues and minimize damage to surrounding healthy cells. However, the development of NIR-II photoagents remain challenging. In this study, an all-fused-ring quinoidal acceptor-donor-acceptor (A-D-A) molecule, SKCN, with a BTP core is synthesized, and nanoparticles named FA-SNPs are prepared. The unique quinoidal structure enhances π-electron delocalization and bond length uniformity, significantly reducing the bandgap of SKCN, resulting in strong NIR-II absorption, a high molar extinction coefficient, and a photothermal conversion efficiency of 75.14%. Enhanced molecular rigidity also facilitates efficient energy transfer to oxygen, boosting reactive oxygen species generation. By incorporating the immunomodulator R848, FA-SRNPs nanoparticles are further developed, effectively modulating the tumor immune microenvironment by reducing Tregs and M-MDSCs infiltration, promoting dendritic cell maturation, M1 macrophage polarization, and activating CD8+ T cells and NK cells. Comprehensive studies using orthotopic ovarian cancer models demonstrated strong tumor targeting, photoacoustic imaging capabilities, and significant tumor suppression and metastasis inhibition, and also showing excellent therapeutic efficacy in an orthotopic breast cancer model. This study provides strong evidence for the potential application of quinoidal A-D-A molecules in cancer photoimmunotherapy.

摘要

具有超高近红外二区(NIR-II)光能转换效率的光试剂在肿瘤光疗中具有巨大潜力,因为它们能够穿透更深的组织并将对周围健康细胞的损伤降至最低。然而,NIR-II光试剂的开发仍然具有挑战性。在本研究中,合成了一种具有BTP核的全稠环醌型受体-供体-受体(A-D-A)分子SKCN,并制备了名为FA-SNPs的纳米颗粒。独特的醌型结构增强了π电子离域和键长均匀性,显著降低了SKCN的带隙,导致强烈的NIR-II吸收、高摩尔消光系数和75.14%的光热转换效率。增强的分子刚性还促进了向氧的有效能量转移,增强了活性氧的产生。通过掺入免疫调节剂R848,进一步开发了FA-SRNPs纳米颗粒,通过减少调节性T细胞(Tregs)和髓系来源的抑制性细胞(M-MDSCs)浸润、促进树突状细胞成熟、M1巨噬细胞极化以及激活CD8+T细胞和自然杀伤细胞(NK细胞),有效地调节肿瘤免疫微环境。使用原位卵巢癌模型进行的综合研究表明,其具有强大的肿瘤靶向性、光声成像能力以及显著的肿瘤抑制和转移抑制作用,并且在原位乳腺癌模型中也显示出优异的治疗效果。本研究为醌型A-D-A分子在癌症光免疫治疗中的潜在应用提供了有力证据。

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