Li Wenjing, Zha Xiaochuan, Zhang Xiaoyu, Dai Haixin, Pu Suyun, Yao Xinya, Hui Wenxue, Xu Rui, Bao Junyu, Yu Jiahao, Wei Yan, Huang Jiawen, Guo Na, Xu Ming, Zhao Jian, Cheng Bingbing, Luo Zonghua
School of Biomedical Engineering & State Key Laboratory of Advanced Medical Materials and Devices, ShanghaiTech University, Shanghai 201210, China.
School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
ACS Chem Neurosci. 2025 Aug 6;16(15):3070-3081. doi: 10.1021/acschemneuro.5c00476. Epub 2025 Jul 28.
Focused ultrasound (FUS)-mediated blood-brain barrier (BBB) opening is an innovative approach for enhancing the delivery of central nervous system drugs. Ga radiotracers are advantageous for imaging due to their ideal half-life and imaging properties; however, their limited ability to traverse the BBB constrains their application in brain imaging. This study investigates the application of FUS to selectively deliver the Ga radiotracer, [Ga]STZL4110, into the hippocampus for β-amyloid positron emission tomography (PET) imaging in an Alzheimer's disease (AD) mouse model. The synthesis and radiolabeling of [Ga]STZL4110 were accomplished, demonstrating robust binding to β-amyloid, as validated by Thioflavin T assays and autoradiography with both wild-type (WT) and APP/PS1 AD mouse brain sections. Cavitation activity measurements confirmed effective and consistent BBB opening post-FUS treatment, ensuring targeted delivery without vascular damage, as supported by histological analysis. Quantitative PET imaging revealed the successful detection of β-amyloid deposition following FUS treatment. Initially, [Ga]STZL4110 showed a low volume of distribution in the right hippocampus of AD mice. FUS application significantly enhanced BBB permeability, leading to a 74% increase in [Ga]STZL4110 uptake in the targeted right hippocampus of APP/PS1 mice compared with the left hippocampus, whereas no significant change was observed in WT mice. These findings suggest that combining FUS with [Ga]STZL4110 could significantly enhance the sensitivity and specificity of Ga PET imaging for β-amyloid. FUS-mediated PET imaging may potentially address the challenge of effective brain imaging with radiotracers that traditionally exhibit a low penetration of the BBB.
聚焦超声(FUS)介导的血脑屏障(BBB)开放是一种增强中枢神经系统药物递送的创新方法。镓放射性示踪剂因其理想的半衰期和成像特性而有利于成像;然而,它们穿越血脑屏障的能力有限,限制了它们在脑成像中的应用。本研究调查了FUS在阿尔茨海默病(AD)小鼠模型中选择性地将镓放射性示踪剂[Ga]STZL4110递送至海马体用于β淀粉样蛋白正电子发射断层扫描(PET)成像的应用。完成了[Ga]STZL4110的合成和放射性标记,通过硫黄素T测定以及野生型(WT)和APP/PS1 AD小鼠脑切片的放射自显影验证,证明其与β淀粉样蛋白有强烈结合。空化活性测量证实了FUS治疗后血脑屏障开放有效且一致,组织学分析支持了这一点,确保了靶向递送而无血管损伤。定量PET成像显示FUS治疗后成功检测到β淀粉样蛋白沉积。最初,[Ga]STZL4110在AD小鼠右侧海马体中的分布容积较低。与左侧海马体相比,FUS应用显著增强了血脑屏障通透性,导致APP/PS1小鼠靶向右侧海马体中[Ga]STZL4110摄取增加74%,而WT小鼠未观察到显著变化。这些发现表明,将FUS与[Ga]STZL4110相结合可以显著提高镓PET成像对β淀粉样蛋白的敏感性和特异性。FUS介导的PET成像可能潜在地解决传统上血脑屏障穿透率低的放射性示踪剂有效脑成像的挑战。