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铟基近红外发射量子点在鼠转移性乳腺癌模型中前哨淋巴结的可视化。

Visualisation of sentinel lymph node with indium-based near infrared emitting Quantum Dots in a murine metastatic breast cancer model.

机构信息

Université de Lorraine, Centre de Recherche en Automatique de Nancy (CRAN), UMR 7039, Vandoeuvre-lès-Nancy, France.

出版信息

PLoS One. 2012;7(8):e44433. doi: 10.1371/journal.pone.0044433. Epub 2012 Aug 30.

Abstract

Due to its non-invasiveness, high temporal resolution and lower cost, fluorescence imaging is an interesting alternative to the current method (blue dye and radiocolloid) of sentinel lymph node (SLN) mapping in breast cancer. Near-infrared (NIR) emitting cadmium-based Quantum Dots (QDs) could be used for this purpose; however, their wide application is limited because of the toxicity of heavy metals composing the core. Our recent work demonstrated that indium-based QDs exhibit a weak acute local toxicity in vivo compared to their cadmium-based counterparts. In the present study we confirmed the weak toxicity of CuInS(2)/ZnS QDs in different in vitro models. Further in vivo studies in healthy mice showed that In-based QDs could be visualised in SLN in a few minutes after administration with a progressive increase in fluorescence until 8 h. The quantity of indium was assessed in selected organs and tissues by inductively coupled plasma - mass spectroscopy (ICP-MS) as a function of post-injection time. QD levels decrease rapidly at the injection point in the first hours after administration with a parallel increase in the lymph nodes and to a lesser extent in the liver and spleen. In addition, we observed that 3.5% of the injected indium dose was excreted in faeces in the first 4 days, with only trace quantities in the urine. Metastatic spread to the lymph nodes may hamper its visualisation. Therefore, we further performed non-invasive fluorescence measurement of QDs in SLN in tumour-bearing mice. Metastatic status was assessed by immunohistology and molecular techniques and revealed the utmost metastatic invasion of 36% of SLN. Fluorescence signal was the same irrespective of SLN status. Thus, near-infrared emitting cadmium-free QDs could be an excellent SLN tracer.

摘要

由于其非侵入性、高时间分辨率和低成本,荧光成像是当前乳腺癌前哨淋巴结 (SLN) 示踪方法(蓝色染料和放射性胶体)的一种有趣替代方法。近红外 (NIR) 发射的基于镉的量子点 (QD) 可用于此目的;然而,由于组成核心的重金属的毒性,它们的广泛应用受到限制。我们最近的工作表明,与基于镉的 QD 相比,基于铟的 QD 在体内表现出较弱的急性局部毒性。在本研究中,我们在不同的体外模型中证实了 CuInS(2)/ZnS QD 的弱毒性。进一步在健康小鼠体内研究表明,基于 In 的 QD 在给药后几分钟内即可在 SLN 中可视化,荧光强度逐渐增加,直到 8 小时。通过电感耦合等离子体质谱 (ICP-MS) 作为注射后时间的函数,在选定的器官和组织中评估铟的数量。给药后最初几小时,在注射部位 QD 水平迅速下降,淋巴结中平行增加,在肝脏和脾脏中则略有增加。此外,我们观察到在最初的 4 天内,有 3.5%的注射铟剂量通过粪便排出,尿液中只有痕量。转移到淋巴结可能会阻碍其可视化。因此,我们进一步在荷瘤小鼠中进行了 SLN 中 QD 的非侵入性荧光测量。通过免疫组织化学和分子技术评估转移状态,结果显示 SLN 的转移入侵率最高为 36%。荧光信号与 SLN 状态无关。因此,近红外发射的无镉 QD 可能是一种出色的 SLN 示踪剂。

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