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AGuIX 纳米颗粒的定量组织药代动力学和 EPR 效应:在原位脑胶质瘤大鼠模型和健康食蟹猴中的多模态成像研究。

Quantitative Tissue Pharmacokinetics and EPR Effect of AGuIX Nanoparticles: A Multimodal Imaging Study in an Orthotopic Glioblastoma Rat Model and Healthy Macaque.

机构信息

Laboratoire d'Imagerie Biomédicale Multimodale Paris Saclay, CEA/INSERM/CNRS/Université Paris-Saclay, Orsay, 91401, France.

Institut Lumière Matière, Université Claude Bernard Lyon I, CNRS UMR 5306, Villeurbanne, 69622, France.

出版信息

Adv Healthc Mater. 2021 Aug;10(16):e2100656. doi: 10.1002/adhm.202100656. Epub 2021 Jul 1.

DOI:10.1002/adhm.202100656
PMID:34212539
Abstract

AGuIX are emerging radiosensitizing nanoparticles (NPs) for precision radiotherapy (RT) under clinical evaluation (Phase 2). Despite being accompanied by MRI thanks to the presence of gadolinium (Gd) at its surface, more sensitive and quantifiable imaging technique should further leverage the full potential of this technology. In this study, it is shown that Zr can be labeled on such NPs directly for positron emission tomography (PET) imaging with a simple and scalable method. The stability of such complexes is remarkable in vitro and in vivo. Using a glioblastoma orthotopic rat model, it is shown that injected Zr-AGuIX is detectable inside the tumor for at least 1 week. Interestingly, the particles seem to efficiently infiltrate the tumor even in necrotic areas, which places great hope for the treatment of radioresistant tumor. Lastly, the first PET/MR whole-body imaging is performed in non-human primate (NHP), which further demonstrates the translational potential of these bimodal NP.

摘要

AGuIX 是一种新兴的放射增敏纳米颗粒(NPs),正在临床评估(二期)中用于精准放疗(RT)。尽管由于表面存在钆(Gd),它可以伴随磁共振成像(MRI),但更敏感和可量化的成像技术应该进一步挖掘这项技术的全部潜力。在这项研究中,结果表明,可以使用一种简单且可扩展的方法直接对这些 NPs 进行标记,用于正电子发射断层扫描(PET)成像。这些配合物的稳定性在体外和体内都非常显著。通过使用胶质母细胞瘤原位大鼠模型,结果表明,注射的 Zr-AGuIX 在肿瘤内至少可检测到 1 周。有趣的是,即使在坏死区域,这些粒子似乎也能有效地渗透到肿瘤中,这为治疗耐辐射肿瘤带来了很大希望。最后,在非人类灵长类动物(NHP)中进行了首次 PET/MR 全身成像,进一步证明了这些双模态 NP 的转化潜力。

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