Yang Zuo, Ji Yu, Jia Qian, Feng Yanbin, Ji Renchuan, Bai Mingli, Yan Haohao, Sun Fang, Zhang Ruili, Wang Zhongliang
Lab of Molecular Imaging and Translational Medicine (MITM), Engineering Research Center of Molecular & Neuro-imaging, Ministry of Education, School of Life Science and Technology, Xidian University, Xi'an, Shaanxi, 710126, People's Republic of China.
Mater Today Bio. 2024 Jul 30;28:101166. doi: 10.1016/j.mtbio.2024.101166. eCollection 2024 Oct.
Sentinel lymph node (SLN) biopsy is a commonly employed procedure for the routine assessment of axillary involvement in patients with breast cancer. Nevertheless, conventional SLN mapping cannot reliably distinguish the presence and absence of metastatic disease. Additionally, the complex anatomical structures and lymphatic drainage patterns surrounding tumor sites pose challenges to the sensitivity of the near-infrared fluorescence imaging with subcutaneously injected probes. To identifying the SLN metastases, we developed a novel nanoprobe for fluorescence imaging within the second near-infrared (NIR-II) range. This nanoprobe utilizes rare-earth nanoparticles (RENPs) to emit bright fluorescence at 1525 nm and is conjugated with tumor-targeted hyaluronic acid (HA) to facilitate the detection of metastatic SLN. Upon intravenous administration, RENPs@HA effectively migrated to SLNs and selectively entered metastatic breast tumor cells through CD44-mediated endocytosis. The RENPs@HA nanoprobes exhibited rapid accumulation in metastatic inguinal lymph nodes in mouse model, displaying a 5.8-fold-stronger fluorescence intensity to that observed in normal SLNs. Consequently, these nanoprobes effectively differentiate metastatic SLNs from normal SLNs. Importantly, the probes accurately detected micrometastases. These findings underscore the potential of RENPs@HA for real-time visualization and screening of SLNs metastasis.
前哨淋巴结(SLN)活检是评估乳腺癌患者腋窝受累情况的常用常规方法。然而,传统的SLN定位无法可靠地区分是否存在转移疾病。此外,肿瘤部位周围复杂的解剖结构和淋巴引流模式对皮下注射探针的近红外荧光成像的敏感性构成了挑战。为了识别SLN转移,我们开发了一种新型纳米探针用于第二近红外(NIR-II)范围内的荧光成像。这种纳米探针利用稀土纳米颗粒(RENPs)在1525nm处发出明亮荧光,并与肿瘤靶向透明质酸(HA)偶联,以促进对转移性SLN的检测。静脉注射后,RENPs@HA有效地迁移到SLN,并通过CD44介导的内吞作用选择性地进入转移性乳腺肿瘤细胞。RENPs@HA纳米探针在小鼠模型的转移性腹股沟淋巴结中表现出快速积累,荧光强度比正常SLN中观察到的强5.8倍。因此,这些纳米探针有效地将转移性SLN与正常SLN区分开来。重要的是,这些探针准确地检测到了微转移。这些发现强调了RENPs@HA在实时可视化和筛查SLN转移方面的潜力。