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经寿命工程设计的近红外二区纳米颗粒实现了多重体内成像。

Lifetime-engineered NIR-II nanoparticles unlock multiplexed in vivo imaging.

机构信息

Department of Chemistry, State Key Laboratory of Molecular Engineering of Polymers, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials and iChem, Fudan University, Shanghai, China.

ARC Centre of Excellence for Nanoscale BioPhotonics (CNBP), Department of Physics and Astronomy, Macquarie University, Sydney, New South Wales, Australia.

出版信息

Nat Nanotechnol. 2018 Oct;13(10):941-946. doi: 10.1038/s41565-018-0221-0. Epub 2018 Aug 6.

Abstract

Deep tissue imaging in the second near-infrared (NIR-II) window holds great promise for physiological studies and biomedical applications. However, inhomogeneous signal attenuation in biological matter hampers the application of multiple-wavelength NIR-II probes to multiplexed imaging. Here, we present lanthanide-doped NIR-II nanoparticles with engineered luminescence lifetimes for in vivo quantitative imaging using time-domain multiplexing. To achieve this, we have devised a systematic approach based on controlled energy relay that creates a tunable lifetime range spanning three orders of magnitude with a single emission band. We consistently resolve selected lifetimes from the NIR-II nanoparticle probes at depths of up to 8 mm in biological tissues, where the signal-to-noise ratio derived from intensity measurements drops below 1.5. We demonstrate that robust lifetime coding is independent of tissue penetration depth, and we apply in vivo multiplexing to identify tumour subtypes in living mice. Our results correlate well with standard ex vivo immunohistochemistry assays, suggesting that luminescence lifetime imaging could be used as a minimally invasive approach for disease diagnosis.

摘要

深层组织在近红外二区(NIR-II)的成像在生理研究和生物医学应用方面具有广阔的前景。然而,生物组织中不均匀的信号衰减限制了多波长近红外二区探针在多路复用成像中的应用。在这里,我们提出了一种基于受激辐射能量传递的方法,通过该方法制备了具有可调谐荧光寿命的镧系掺杂纳米粒子,可用于基于时间域复用的活体定量成像。我们设计了一种基于受激辐射能量传递的方法,该方法可以在单个发射带中创建一个可调谐的寿命范围,跨越三个数量级。我们在生物组织中深度可达 8mm 的范围内,始终可以分辨出来自 NIR-II 纳米粒子探针的选定寿命,在这个深度范围内,源于强度测量的信噪比降至 1.5 以下。我们证明了稳健的寿命编码与组织穿透深度无关,并将体内多路复用技术应用于活体小鼠中识别肿瘤亚型。我们的结果与标准的离体免疫组织化学分析相关性良好,这表明荧光寿命成像可作为疾病诊断的微创方法。

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