X-ray/red-light excited ZGGO:Cr, Nd nanoprobes for NIR-I/II afterglow imaging. Issue 18 (22nd April 2020)

• Record Type: Journal Article
• Authors: Jiang, Rongyun; Yang, Jian; Meng, Yangqi; Yan, Duanting; Liu, Chunguang; Xu, Changshan; Liu, Yuxue
• Is Part Of: Dalton transactions. Volume 49:Issue 18(2020)
• Page Start: 6074
• Page End: 6083
• Publication Date: 2020-04-22
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d0dt00247j
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : NIR-I/II afterglow nanoprobes for deep-tissue autofluorescence-free bioimaging were developed based on the persistent energy transfer. Abstract : Zn2 Ga3− x − y Cr x Nd y Ge0.75 O8 (ZGGO:Cr x, Nd y ) persistent luminescent nanoparticles (PLNPs) ( x = 0, 0.02; and y = 0, 0.01, 0.02, 0.03, 0.04) were synthesized via a hydrothermal method in combination with a following heat treatment under vacuum. The effects of Nd 3+ concentration on chemical composition, size distribution, luminescence property, the persistent energy transfer from Cr 3+ to Nd 3+ and afterglow imaging were studied in detail. When the Nd 3+ concentration was increased from 0 to 0.04, the particle size increased from 45.4 to 86.2 nm. The afterglow emissions in the NIR-I (696 nm) and NIR-II (1067 nm) regions, which are ascribed to the 2 E, 4 T2 → 4 A2 transitions of Cr 3+ and the 4 F3/2 → 4 I11/2 transition of Nd 3+, respectively, were simultaneously acquired after stopping the 635 nm excitation. Among the nanoparticles with different concentrations, ZGGO:Cr0.02, Nd0.02 exhibits the strongest NIR-II afterglow intensity and the corresponding energy transfer efficiency from Cr 3+ to Nd 3+ is found to be 25.9%. In addition, enhanced X-ray excited afterglow imaging can be observed in Nd 3+ /Cr 3+ codoped nanoparticles dispersed in water, human serum albumin solution and simulated lysosomal environment compared to the Cr 3+ singly doped nanoparticles. Renewable NIR afterglow imaging was realized through an X-ray reexcitation strategy. In particular, both the X-ray excitation strategy accompanied by NIR-I afterglow emission and the red light (635 nm) excitation strategy accompanied by NIR-II afterglow emission exhibit high tissue penetration capability. This study provides a further understanding of how to develop a suitable strategy for realizing deep tissue autofluorescence-free bioimaging.