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患者来源细胞外囊泡的临床前药理学用于肿瘤术中成像。

Preclinical pharmacology of patient-derived extracellular vesicles for the intraoperative imaging of tumors.

机构信息

Department of Health Sciences, University of Milan, Milan, Italy.

Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.

出版信息

Theranostics. 2024 Sep 30;14(16):6301-6318. doi: 10.7150/thno.98671. eCollection 2024.

Abstract

Extracellular vesicles (EVs) derived from the plasma of oncological patients exhibit significant tumor-targeting properties, unlike those from healthy individuals. We have previously shown the feasibility of formulating the near-infrared (NIR) fluorescent dye indocyanine green (ICG) with patient-derived extracellular vesicles (PDEVs) for selective delivery to neoplastic tissue. This staining protocol holds promise for clinical application in intraoperative tumor margin imaging, enabling precise neoplastic tissue resection. To this end, we propose the ONCOGREEN protocol, involving PDEV isolation, ICG loading, and reinfusion into the same patients. : By in vivo studies on mice, we outlined key pharmacological parameters of PDEVs-ICG for intraoperative tumor imaging, PDEV biodistribution kinetics, and potential treatment-related toxicological effects. Additionally, we established a plasmapheresis-based protocol for isolating autologous PDEVs, ensuring the necessary large-scale dosage for human treatment. A potential lyophilization-based preservation method was also explored to facilitate the storage and transport of PDEVs. : The study identified the effective dose of PDEVs-ICG necessary for clear intraoperative tumor margin imaging. The biodistribution kinetics of PDEVs showed favorable targeting to neoplastic tissues, without off-target distribution. Toxicological assessments revealed no significant adverse effects associated with the treatment. The plasmapheresis-based isolation protocol successfully yielded a sufficient quantity of autologous PDEVs, and the lyophilization preservation method maintained the functional integrity of PDEVs for subsequent clinical application. : Our research lays the groundwork for the direct clinical application of autologous PDEVs, initially focusing on intraoperative imaging. Utilizing autologous PDEVs has the potential to accelerate the integration of EVs as a targeted delivery tool for anti-neoplastic agents to cancerous tissue. This approach promises to enhance the precision of neoplastic tissue resection and improve overall surgical outcomes for oncological patients.

摘要

源自肿瘤患者血浆的细胞外囊泡 (EVs) 表现出明显的肿瘤靶向特性,这与来自健康个体的 EVs 不同。我们之前已经证明了将近红外 (NIR) 荧光染料吲哚菁绿 (ICG) 与患者来源的细胞外囊泡 (PDEVs) 制剂化用于选择性递送至肿瘤组织的可行性。这种染色方案有望在术中肿瘤边界成像的临床应用中得到应用,从而实现对肿瘤组织的精确切除。为此,我们提出了 ONCOGREEN 方案,包括 PDEV 的分离、ICG 的加载以及将其重新注入同一患者体内。

通过在小鼠体内研究,我们概述了 PDEV-ICG 用于术中肿瘤成像的关键药代动力学参数、PDEV 生物分布动力学以及潜在的与治疗相关的毒理学效应。此外,我们建立了一种基于血浆分离的自体 PDEV 分离方案,以确保用于人类治疗的必要大剂量。还探索了一种潜在的基于冷冻干燥的保存方法,以促进 PDEV 的储存和运输。

研究确定了用于清晰术中肿瘤边界成像的 PDEV-ICG 的有效剂量。PDEV 的生物分布动力学显示对肿瘤组织具有良好的靶向性,没有脱靶分布。毒理学评估显示与治疗相关的无显著不良反应。基于血浆分离的分离方案成功获得了足够数量的自体 PDEV,冷冻干燥保存方法保持了 PDEV 的功能完整性,以便随后的临床应用。

我们的研究为直接将自体 PDEV 应用于临床奠定了基础,最初侧重于术中成像。利用自体 PDEV 有可能加速将 EV 作为一种靶向递药工具用于将抗肿瘤药物递送至肿瘤组织。这种方法有望提高肿瘤组织切除的精度,并改善肿瘤患者的整体手术效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57f8/11488097/8b733c3fe376/thnov14p6301g001.jpg

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