Feasibility of label-free multiphoton luminescence imaging to track the fate of inhaled gold nanoparticles in ex vivo lung tissue.

Biophotonics discovery Pub Date : 2026-09-29 eCollection Date: 2026-10-01 DOI:10.1117/1.BIOS.3.4.043105
Sean Burkitt, Olga Eremina, Alexander Czaja, Boyi Wang, William Wallace, Cristina Zavaleta
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Abstract

Significance: Understanding the biological journey of inhaled gold nanomaterials is critical for nanotoxicology and therapeutic delivery. Conventional tracking methods often require fluorescent labeling, which can alter nanoparticle (NP) surface chemistry and lead to "false-positive" signals if the label dissociates.

Aim: In this feasibility study, we utilize multiphoton luminescence (MPL) imaging to track the long-term biodistribution of 50 nm AuNPs following inhalation exposure at 1 week and 1 month.

Approach: Mice were administered AuNPs via intranasal inhalation in four experimental groups: low (0.1 nM), medium (1 nM), high (10 nM) doses for 1 week, and a medium dose (1 nM) for 1 month. Organs were harvested and analyzed using ICP-MS for total gold content and MPL imaging for label-free visualization of AuNP deposition.

Results: AuNPs remained localized within the lungs with no evidence of systemic translocation to the liver, spleen, brain, or kidneys at either time point. MPL imaging revealed that lung concentration followed a linear scaling model at one week. MPL imaging also revealed the long-term identification and localization of AuNPs within the lung at 1 month postinhalation.

Conclusions: MPL imaging is superior to brightfield microscopy for NP detection, enabling the visualization of dose-dependent aggregation and deep-tissue mapping. These findings demonstrate the feasibility of MPL imaging as a label-free complementary imaging approach for pulmonary nanoparticle biodistribution studies.

无标记多光子发光成像在离体肺组织中追踪吸入金纳米颗粒命运的可行性。
意义:了解吸入金纳米材料的生物学过程对纳米毒理学和治疗递送至关重要。传统的跟踪方法通常需要荧光标记,这可以改变纳米颗粒(NP)的表面化学性质,并导致“假阳性”信号,如果标签解离。目的:在这项可行性研究中,我们利用多光子发光(MPL)成像来跟踪吸入暴露后1周和1个月50 nm AuNPs的长期生物分布。方法:将小鼠分为4个实验组:低剂量(0.1 nM)、中剂量(1 nM)、高剂量(10 nM),持续1周,中剂量(1 nM)持续1个月。采集器官并使用ICP-MS分析总含金量,MPL成像用于无标记可视化AuNP沉积。结果:AuNPs仍然局限于肺部,没有证据表明在任何一个时间点都有系统性转移到肝脏、脾脏、大脑或肾脏。MPL成像显示肺浓度在一周后呈线性缩放模型。MPL成像也显示吸入后1个月肺内aunp的长期识别和定位。结论:MPL成像在NP检测方面优于明场显微镜,可以实现剂量依赖性聚集和深部组织定位的可视化。这些发现证明了MPL成像作为肺部纳米颗粒生物分布研究的无标记辅助成像方法的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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