Pr3+ doped NaYF4 and LiYF4 nanocrystals combining visible-to-UVC upconversion and NIR-to-NIR-II downconversion luminescence emissions for biomedical applications

光子上转换 纳米晶 材料科学 光电子学 兴奋剂 发光 镧系元素 激发态 荧光 分析化学(期刊) 纳米技术 光化学 化学 离子 光学 物理 有机化学 色谱法 核物理学 冶金
作者
Min Ying Tsang,Patryk Fałat,Magda A. Antoniak,Roman Ziniuk,Szymon J. Zelewski,Marek Samoć,Marcin Nyk,Junle Qu,Tymish Y. Ohulchanskyy,Dominika Wawrzyńczyk
出处
期刊:Nanoscale [Royal Society of Chemistry]
卷期号:14 (39): 14770-14778 被引量:17
标识
DOI:10.1039/d2nr01680j
摘要

Lanthanide-doped fluoride nanocrystals (NCs) are known to exhibit unique optical properties, such as upconversion and downconversion luminescence (UCL and DCL), which can be employed for various applications. In this work, we demonstrate that by doping praseodymium(III) and ytterbium(III) ions (Pr3+ and Yb3+) into a nanosized fluoride matrix (i.e. NaYF4 and LiYF4), it is possible to combine their UCL and DCL properties that can be concurrently used for biomedical applications. In particular, the emissive modes combined in a single nanoparticle co-doped with Pr3+ and Yb3+ include DCL emission (excited at 980 nm and peaked at 1320 nm), which can be used for near infrared (NIR) DCL bioimaging in the NIR-II window of biological tissue transparency (∼1000-1350 nm) and UCL emission (excited at 447 nm and peaked at 275 nm) that can be employed for germicide action (via irradiation by light in the UVC range). A possibility of the latter was demonstrated by the denaturation of double-stranded DNA (dsDNA) into single-stranded ones that was caused by the UVC UCL emission from the NCs under 447 nm irradiation; it was evidenced by the hyperchromicity observed in the irradiated dsDNA solution and also by a fluorometric analysis of DNA unwinding (FADU) assay. Concurrently, the possibility of NIR-II luminescence bioimaging through biological tissues (bovine tooth and chicken flesh) was demonstrated. The proposed concept paves a way for NIR-II imaging guided antimicrobial phototherapy using lanthanide-doped fluoride nanocrystals.
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