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A new near-infrared persistent luminescence nanoparticle as a multifunctional nanoplatform for multimodal imaging and cancer therapy

机译:一种新的近红外持续发光纳米粒子,作为多峰成像和癌症治疗的多功能纳米片

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摘要

Multifunctional nanoplatforms with multimodal imaging and cancer therapy capabilities have attracted attention in biomedical applications. Near-infrared persistent luminescence nanoparticles (NPLNPs) were considered one of the most promising candidates for constructing multifunctional nanoplatforms due to the absence of in situ excitation and high signal-to-noise ratios (SNRs). Here, we report a novel NPLNP mSiO(2)@Gd(3)GasO(12):Cr3+, Nd3+ (mSiO(2)@GGO) as multifunctional nanoplatforms for multimodal imaging and cancer therapy. These NPs exhibited a persistent luminescence (745 nm) of more than 3 h in the first near-infrared window (NIR-I) after UV excitation, which can realize high SNRs and long-term in vivo imaging. Moreover, these NPs showed excellent NIR luminescence (1067 nm) in the second near-infrared window (NIR-II) under 808 nm excitation, which is more suitable for deep tissue imaging due to the lower photon scattering and deeper tissue penetration of NIR-II luminescence. Furthermore, the host Gd3Ga5O12 with high Gd3+ concentration showed a high r(1) value (10.70 mM(-1) s(-1)) and was suitable for T-1 MR imaging. The mesoporous silica nanoparticles (mSiO(2)) served as a framework to control the mSiO(2)@GGO particle morphology and provide low toxicity and drug loading capacity for cancer therapy. (C) 2017 Elsevier Ltd. All rights reserved.
机译:具有多模式成像和癌症治疗能力的多功能纳米型在生物医学应用中引起了注意力。近红外持续发光纳米颗粒(NPLNPS)被认为是构建多官能纳米孔的最有希望的候选物之一,因为没有原位激发和高信噪比(SNR)。在这里,我们报告了一种新颖的NPLNP MSIO(2)@gd(3)gaso(12):cr3 +,nd3 +(MSIO(2)@gl)作为多峰成像和癌症治疗的多功能纳米载作用。在UV激励之后,在第一近红外窗口(NIR-I)中,这些NPS在第一个近红外窗口(NIR-I)中显示出超过3小时的持续发光(745nm),这可以实现高SNR和长期体内成像。此外,在808nm激发下,这些NPS在第二近红外窗口(NIR-II)中显示出优异的NIR发光(1067nm),其更适合于由于下光子散射和更深的组织渗透而导致的深层组织成像。 II发光。此外,具有高GD3 +浓度的宿主Gd3ga5O12显示出高R(1)值(10.70mm(-1)S(-1)),适用于T-1 MR成像。中孔二氧化硅纳米粒子(MSIO(2))用作控制MSIO(2)@GGO颗粒形态的框架,并为癌症治疗提供低毒性和药物负载能力。 (c)2017 Elsevier Ltd.保留所有权利。

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