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用于体内疾病监测的可清除肾脏的催化金纳米簇。

Renal clearable catalytic gold nanoclusters for in vivo disease monitoring.

机构信息

Department of Materials, Department of Bioengineering, and Institute of Biomedical Engineering, Imperial College London, London, UK.

Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

Nat Nanotechnol. 2019 Sep;14(9):883-890. doi: 10.1038/s41565-019-0527-6. Epub 2019 Sep 2.

Abstract

Ultrasmall gold nanoclusters (AuNCs) have emerged as agile probes for in vivo imaging, as they exhibit exceptional tumour accumulation and efficient renal clearance properties. However, their intrinsic catalytic activity, which can enable an increased detection sensitivity, has yet to be explored for in vivo sensing. By exploiting the peroxidase-mimicking activity of AuNCs and the precise nanometre-size filtration of the kidney, we designed multifunctional protease nanosensors that respond to disease microenvironments to produce a direct colorimetric urinary readout of the disease state in less than one hour. We monitored the catalytic activity of AuNCs in the collected urine of a mouse model of colorectal cancer in which tumour-bearing mice showed a 13-fold increase in colorimetric signal compared to healthy mice. The nanosensors were eliminated completely through hepatic and renal excretion within four weeks of injection with no evidence of toxicity. We envision that this modular approach will enable the rapid detection of a diverse range of diseases by exploiting their specific enzymatic signatures.

摘要

超小的金纳米簇(AuNCs)作为用于体内成像的灵活探针已经出现,因为它们表现出非凡的肿瘤积累和高效的肾脏清除特性。然而,它们的内在催化活性,这可以提高检测灵敏度,还没有被探索用于体内传感。通过利用 AuNCs 的过氧化物酶模拟活性和肾脏的精确纳米级过滤,我们设计了多功能蛋白酶纳米传感器,它们可以响应疾病微环境,在不到一个小时的时间内产生疾病状态的直接比色尿读数。我们监测了在结直肠癌小鼠模型中收集的尿液中 AuNCs 的催化活性,与健康小鼠相比,荷瘤小鼠的比色信号增加了 13 倍。纳米传感器在注射后四周内通过肝和肾排泄完全消除,没有毒性的证据。我们设想,这种模块化方法将通过利用其特定的酶学特征,实现对多种疾病的快速检测。

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