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控制电子陷阱深度以增强用于体内成像的持久发光纳米粒子的光学性质。

Controlling electron trap depth to enhance optical properties of persistent luminescence nanoparticles for in vivo imaging.

机构信息

Unité de Pharmacologie Chimique et Génétique et d'Imagerie, CNRS, UMR 8151, Paris, F-75270 cedex, France.

出版信息

J Am Chem Soc. 2011 Aug 3;133(30):11810-5. doi: 10.1021/ja204504w. Epub 2011 Jul 13.

Abstract

Focusing on the use of nanophosphors for in vivo imaging and diagnosis applications, we used thermally stimulated luminescence (TSL) measurements to study the influence of trivalent lanthanide Ln(3+) (Ln = Dy, Pr, Ce, Nd) electron traps on the optical properties of Mn(2+)-doped diopside-based persistent luminescence nanoparticles. This work reveals that Pr(3+) is the most suitable Ln(3+) electron trap in the diopside lattice, providing optimal trap depth for room temperature afterglow and resulting in the most intense luminescence decay curve after X-ray irradiation. This luminescence dependency toward the electron trap is maintained through additional doping with Eu(2+), allowing UV-light excitation, critical for bioimaging applications in living animals. We finally identify a novel composition (CaMgSi(2)O(6):Eu(2+),Mn(2+),Pr(3+)) for in vivo imaging, displaying a strong near-infrared afterglow centered on 685 nm, and present evidence that intravenous injection of such persistent luminescence nanoparticles in mice allows not only improved but highly sensitive detection through living tissues.

摘要

聚焦于纳米荧光粉在体内成像和诊断应用中的使用,我们利用热激励发光(TSL)测量来研究三价镧系元素 Ln(3+)(Ln = Dy、Pr、Ce、Nd)电子陷阱对掺 Mn(2+)透辉石基持续发光纳米粒子光学性质的影响。这项工作表明,Pr(3+)是透辉石晶格中最适合的 Ln(3+)电子陷阱,提供了室温余晖的最佳陷阱深度,并在 X 射线照射后产生最亮的发光衰减曲线。这种对电子陷阱的发光依赖性通过 Eu(2+)的额外掺杂得以维持,允许进行 UV 光激发,这对活体动物的生物成像应用至关重要。我们最终确定了一种用于体内成像的新型组合物(CaMgSi(2)O(6):Eu(2+),Mn(2+),Pr(3+)),其近红外余晖集中在 685nm 左右,并提供证据表明,静脉注射此类持续发光纳米粒子在小鼠体内不仅可以通过活体组织进行改进,而且可以进行高度敏感的检测。

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