| Literature DB >> 28771315 |
Jie Wang1, Qinqin Ma1, Xiao-Xiao Hu2, Haoyang Liu1, Wei Zheng3, Xueyuan Chen3, Quan Yuan1, Weihong Tan2.
Abstract
Optical bioimaging is an indispensable tool in modern biology and medicine, but the technique is susceptible to autofluorescence interference. Persistent nanophosphors provide an easy-to-perform and highly efficient means to eliminate tissue autofluorescence. However, direct synthesis of persistent nanophosphors with tunable properties to meet different bioimaging requirements remains largely unexplored. In this work, zinc gallogermanate (Zn1+xGa2-2xGexO4:Cr, 0 ≤ x ≤ 0.5, ZGGO:Cr) persistent luminescence nanoparticles with composition-dependent size and persistent luminescence are reported. The size of the ZGGO:Cr nanoparticles gradually increases with the increase of x in the chemical formula. Moreover, the intensity and decay time of persistent luminescence in ZGGO:Cr nanoparticles can also be fine-tuned by simply changing x in the formula. In vivo bioimaging tests demonstrate that ZGGO:Cr nanoparticles can efficiently eliminate tissue autofluorescence, and the nanoparticles also show good promise in long-term bioimaging as they can be easily reactivated in vivo. Furthermore, an aptamer-guided ZGGO:Cr bioprobe is constructed, and it displays excellent tumor-specific accumulation. The ZGGO:Cr nanoparticles are ideal for autofluorescence-free targeted bioimaging, indicating their great potential in monitoring cellular networks and construction of guiding systems for surgery.Entities:
Keywords: aptamer; autofluorescence; bioimaging; nanoparticle; near-infrared light; persistent luminescence
Year: 2017 PMID: 28771315 DOI: 10.1021/acsnano.7b02643
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881