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血管介入放射学引导的治疗诊断一体化金纳米棒用于结直肠癌肝转移的光热治疗。

Vascular Interventional Radiology-Guided Photothermal Therapy of Colorectal Cancer Liver Metastasis with Theranostic Gold Nanorods.

出版信息

ACS Nano. 2018 Jul 24;12(7):6597-6611. doi: 10.1021/acsnano.8b01424. Epub 2018 Jul 6.

Abstract

We report sub-100 nm optical/magnetic resonance (MR)/X-ray contrast-bearing theranostic nanoparticles (TNPs) for interventional image-guided photothermal therapy (PTT) of solid tumors. TNPs were composed of Au@GdO:Ln (Ln = Yb/Er) with X-ray contrast (∼486 HU; 10 NPs/mL, 0.167 nM) and MR contrast (∼1.1 × 10 mM S at 9.4 T field strength). Although TNPs are deposited in tumors following systemic administration via enhanced permeation and retention effect, the delivered dose to tumors is typically low; this can adversely impact the efficacy of PTT. To overcome this limitation, we investigated the feasibility of site-selective hepatic image-guided delivery of TNPs in rats bearing colorectal liver metastasis (CRLM). The mesenteric vein of tumor-bearing rats was catheterized, and TNPs were infused into the liver by accessing the portal vein for site-selective delivery. The uptake of TNPs with hepatic delivery was compared with systemic administration. MR imaging confirmed that delivery via the hepatic portal vein can double the CRLM tumor-to-liver contrast compared with systemic administration. Photothermal ablation was performed by inserting a 100 μm fiber-optic carrying 808 nm light via a JB1, 3-French catheter for 3 min under DynaCT image guidance. Histological analysis revealed that the thermal damage was largely confined to the tumor region with minimal damage to the adjacent liver tissue. Transmission electron microscopy imaging validated the stability of core-shell structure of TNPs in vivo pre- and post-PTT. TNPs comprising Gd-shell-coated Au nanorods can be effectively employed for the site-directed PTT of CRLM by leveraging interventional radiology methods.

摘要

我们报告了亚 100nm 光学/磁共振(MR)/X 射线对比载治疗性纳米颗粒(TNPs),用于实体瘤的介入影像引导光热治疗(PTT)。TNPs 由 Au@GdO:Ln(Ln = Yb/Er)组成,具有 X 射线对比(约 486 HU;10 NPs/mL,0.167 nM)和 MR 对比(在 9.4 T 场强下约为 1.1×10 mM S)。尽管 TNPs 可以通过增强渗透和保留效应在全身给药后沉积在肿瘤中,但输送到肿瘤的剂量通常较低;这可能会对 PTT 的疗效产生不利影响。为了克服这一限制,我们研究了在患有结直肠癌肝转移(CRLM)的大鼠中进行选择性肝图像引导 TNPs 递药的可行性。通过对肿瘤大鼠的肠系膜静脉进行导管插入术,并通过门静脉将 TNPs 输注到肝脏中进行选择性递药。比较了肝内递药与全身给药的 TNPs 摄取情况。MR 成像证实,与全身给药相比,通过肝门静脉给药可以使 CRLM 肿瘤与肝脏的对比增加一倍。通过插入一根带有 808nm 光的 100μm 光纤,在 DynaCT 影像引导下进行 3 分钟的光热消融,通过 JB1、3-French 导管进行。组织学分析显示,热损伤主要局限于肿瘤区域,对相邻肝组织的损伤最小。透射电子显微镜成像验证了 TNPs 的核壳结构在体内 PTT 前后的稳定性。由 Gd 壳包覆的 Au 纳米棒组成的 TNPs 可以通过介入放射学方法有效地用于 CRLM 的靶向 PTT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b434/9272590/a5f405371a77/nihms-980060-f0001.jpg

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