Department of Nuclear Medicine, The Fourth Hospital of Harbin Medical University, Harbin 150028, China.
NHC Key Laboratory of Molecular Probe and Targeted Diagnosis and Therapy, Molecular Imaging Research Center (MIRC), Harbin Medical University, Harbin 150028, China.
Nano Lett. 2023 Apr 12;23(7):2964-2973. doi: 10.1021/acs.nanolett.3c00354. Epub 2023 Mar 22.
Recent advances in intratracheal delivery strategies have sparked considerable biomedical interest in developing this promising approach for lung cancer diagnosis and treatment. However, there are very few relevant studies on the behavior and mechanism of imaging nanoparticles (NPs) after intratracheal delivery. Here, we found that nanosized perfluoro-15-crown-5-ether (PFCE NPs, ∼200 nm) exhibite significant F-MRI signal-to-noise ratio (SNR) enhancement than perfluorooctyl bromide (PFOB NPs) up to day 7 after intratracheal delivery. Alveolar macrophages (AMs) engulf PFCE NPs, become PFCE NPs-laden AMs, and then migrate into the tumor margin, resulting in increased tumor PFCE concentration and F-MRI signals. AMs-mediated translocation of PFCE NPs to lung draning lymph nodes (dLNs) decreases the background PFCE concentration. Our results shed light on the dynamic AMs-mediated translocation of intratracheally delivered PFC NPs for effective lung tumor visualization and reveal a pathway to develop and promote the clinical translation of an intratracheal delivery-based imaging strategy.
近年来,经气管内递药策略的进展引起了生物医学领域极大的兴趣,人们希望将这一很有前途的方法用于肺癌的诊断和治疗。然而,关于气管内给药后成像纳米颗粒(NPs)的行为和机制的相关研究却很少。在这里,我们发现,纳米级全氟-15-冠-5-醚(PFCE NPs,∼200nm)在气管内给药后 7 天内表现出比全氟辛基溴化物(PFOB NPs)更高的 F-MRI 信噪比(SNR)增强。肺泡巨噬细胞(AMs)吞噬 PFCE NPs,成为负载 PFCE NPs 的 AMs,然后迁移到肿瘤边缘,导致肿瘤中 PFCE 浓度和 F-MRI 信号增加。AMs 介导的 PFCE NPs 向肺引流淋巴结(dLNs)的转运减少了背景 PFCE 浓度。我们的研究结果阐明了经气管内递药的 PFC NPs 被肺泡巨噬细胞动态转运,用于有效肺部肿瘤可视化,并揭示了开发和促进基于气管内递药的成像策略的临床转化的途径。