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基于近红外至近红外(NIR-to-NIR)上转换发光和磁共振性质的稀土纳米晶体的双模式体内成像。

Dual-modality in vivo imaging using rare-earth nanocrystals with near-infrared to near-infrared (NIR-to-NIR) upconversion luminescence and magnetic resonance properties.

机构信息

Department of Chemistry & Advanced Materials Laboratory, Fudan University, Shanghai, PR China.

出版信息

Biomaterials. 2010 Apr;31(12):3287-95. doi: 10.1016/j.biomaterials.2010.01.040. Epub 2010 Feb 4.

Abstract

Upconversion luminescence (UCL) imaging is expected to play a significant role in future photoluminescence imaging since it shows advantages of sharp emission lines, long lifetimes, superior photostability and no blinking. To further improve penetration depth, herein, near-infrared to near-infrared (NIR-to-NIR) UCL and magnetic properties were combined into a nanoparticle, and NIR-to-NIR UCL and MRI dual-modal bioimaging in vivo of whole-body animal were developed. Hydrophilic and carboxylic acid-functionalized Tm(3+)/Er(3+)/Yb(3+) co-doped NaGdF(4) upconversion nanophosphors (AA-NPs) were synthesized and showed both NIR-to-visible and NIR-to-NIR luminescence under excitation of 980 nm. Collecting the signal of the upconversion emission from AA-NPs in the visible and NIR range, all UCL imaging of cells, tissues and whole-body animals with different penetration depth showed high contrast. Moreover, AA-NPs showed a high relaxivity of 5.60 s(-1) (mM)(-1) and were successfully applied as contrast agents for magnetic resonance imaging (MRI) in vivo. By means of the combination of UCL imaging and MRI, the distribution of AA-NPs in living animals was studied, and the results indicated that these particles mainly accumulate in the liver and spleen without undesirable stay in the lungs. Therefore, the concept of UCL and MR dual-modality imaging in vivo of whole-body animals using Tm(3+)/Er(3+)/Yb(3+) co-doped NaGdF(4) with NIR-to-NIR upconversion luminescent and magnetic resonance properties can serve as a platform technology for the next-generation of probes for bioimaging in vivo.

摘要

上转换发光(UCL)成像是未来光致发光成像的重要手段,因为它具有发射线尖锐、寿命长、光稳定性好、无闪烁等优点。为了进一步提高穿透深度,本文将近红外到近红外(NIR-to-NIR)上转换发光和磁性结合到一个纳米颗粒中,开发了用于活体全动物 NIR-to-NIR UCL 和 MRI 双模式生物成像。合成了亲水性和羧酸功能化的 Tm(3+)/Er(3+)/Yb(3+)共掺杂 NaGdF(4)上转换纳米荧光粉(AA-NPs),在 980nm 激发下显示出近红外到可见和近红外到近红外发光。收集 AA-NPs 在可见和近红外范围内的上转换发射信号,具有不同穿透深度的细胞、组织和全动物的所有 UCL 成像均显示出高对比度。此外,AA-NPs 的弛豫率高达 5.60 s(-1)(mM)(-1),成功用作体内磁共振成像(MRI)的造影剂。通过 UCL 成像和 MRI 的结合,研究了 AA-NPs 在活体内的分布,结果表明这些颗粒主要积聚在肝脏和脾脏中,而不在肺部积聚。因此,使用具有 NIR-to-NIR 上转换发光和磁共振性质的 Tm(3+)/Er(3+)/Yb(3+)共掺杂 NaGdF(4)进行活体全动物 UCL 和 MR 双模式成像的概念可以作为下一代活体生物成像探针的平台技术。

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