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基于金纳米棒的核-卫星多功能纳米诊疗剂用于体内磁共振和计算机断层成像以及协同光热与放射敏感治疗

PB@Au Core-Satellite Multifunctional Nanotheranostics for Magnetic Resonance and Computed Tomography Imaging in Vivo and Synergetic Photothermal and Radiosensitive Therapy.

机构信息

School of Life Sciences, School of Material Science and Engineering, Tianjin University, Tianjin Engineering Center for Micro-Nano Biomaterials and Detection-Treatment Technology , Tianjin 300072, PR China.

Department of Radiology, Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital , Tianjin 300052, PR China.

出版信息

ACS Appl Mater Interfaces. 2017 Jan 18;9(2):1263-1272. doi: 10.1021/acsami.6b13493. Epub 2017 Jan 6.

Abstract

To integrate multiple diagnostic and therapeutic strategies on a single particle through simple and effective methods is still challenging for nanotheranostics. Herein, we develop multifunctional nanotheranostic PB@Au core-satellite nanoparticles (CSNPs) based on Prussian blue nanoparticles (PBNPs) and gold nanoparticles (AuNPs), which are two kinds of intrinsic theranostic nanomaterials, for magnetic resonance (MR)-computed tomography (CT) imaging and synergistic photothermal and radiosensitive therapy (PTT-RT). PBNPs as cores enable T- and T-weighted MR contrast and strong photothermal effect, while AuNPs as satellites offer CT enhancement and radiosensitization. As revealed by both MR and CT imaging, CSNPs realized efficient tumor localization by passively targeted accumulation after intravenous injection. In vivo studies showed that CSNPs resulted in synergistic PTT-RT action to achieve almost entirely suppression of tumor growth without observable recurrence. Moreover, no obvious systemic toxicity of mice confirmed good biocompatibility of CSNPs. These results raise new possibilities for clinical nanotheranostics with multimodal diagnostic and therapeutic coalescent design.

摘要

通过简单有效的方法将多种诊断和治疗策略集成到单个颗粒上,对于纳米治疗仍然是一个挑战。在此,我们开发了基于普鲁士蓝纳米颗粒(PBNPs)和金纳米颗粒(AuNPs)的多功能纳米治疗 PB@Au 核-卫星纳米颗粒(CSNPs),这两种材料都是内在的治疗纳米材料,可用于磁共振(MR)-计算机断层扫描(CT)成像以及协同光热和放射敏感治疗(PTT-RT)。PBNPs 作为核心赋予 T1 和 T2 加权 MR 对比和强光热效应,而 AuNPs 作为卫星提供 CT 增强和放射增敏作用。通过 MR 和 CT 成像显示,CSNPs 经静脉注射后通过被动靶向积累实现了有效的肿瘤定位。体内研究表明,CSNPs 产生协同的 PTT-RT 作用,几乎完全抑制肿瘤生长而无明显复发。此外,小鼠无明显的全身毒性证实了 CSNPs 的良好生物相容性。这些结果为具有多模态诊断和治疗融合设计的临床纳米治疗提供了新的可能性。

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