镧系元素
发光
材料科学
纳米颗粒
自体荧光
兴奋剂
纳米技术
化学
离子
光电子学
荧光
光学
有机化学
物理
作者
Lin Liu,Junpeng Shi,Shanshan Peng,Hongyun Zhong,Peng Lin,Jin‐Yuan Wang,Xia Sun,Liang Song,Quan Yuan,Yun Zhang
标识
DOI:10.1007/s40843-022-2404-0
摘要
The near-infrared-II (NIR-II) lanthanide-doped inorganic nanoparticles (NPs) have received considerable attention because of their low photon scattering and autofluorescence for deep tissue penetration. These NIR-II NPs have a “rigid” and physiologically inert crystal lattice (such as NaYF4:Yb,Er) and cannot be degraded in vivo, limiting their biomedical applications. Changing the chemical structure to achieve the transition from “rigid” to “soft” crystals is a feasible method for realizing their biodegradable applications. Herein, we developed a type of biodegradable NIR-IIb lanthanide-doped inorganic NPs, Na3ZrF7:Yb,Er,Ce (NZF). By optimizing the regulation of Na and doping with Ce3+, the NIR-IIb down-conversion luminescence (DCL) intensity of NZF NPs increased 37 times compared with Na3ZrF7:Yb,Er. Additionally, because of their “soft” crystal lattice features, water can destroy their crystal structure, and the degradation products can be excreted from the organs and tissues. Furthermore, NZF NPs exhibit red-emitting up-conversion luminescence (UCL). After surface modifications, we performed the proof of concept in biodegradable bioimaging applications and photodynamic therapy based on their NIR-IIb DCL and red-emitting UCL. These findings will benefit the future biomedical applications of lanthanide-doped inorganic NPs.
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