ZnAl 2 O 4 :Er 3+ Upconversion Nanophosphor for SPECT Imaging and Luminescence Modulation via Defect Engineering.
Annu BalharaSantosh Kumar GuptaKathi SudarshanSourav PatraAvik ChakrabortySudipta ChakrabortyPublished in: ACS applied bio materials (2024)
This work reports an "all-in-one" theranostic upconversion luminescence (UCL) system having potential for both diagnostic and therapeutic applications. Despite considerable efforts in designing upconversion nanoparticles (UCNPs) for multimodal imaging and tumor therapy, there are few reports investigating dual modality SPECT/optical imaging for theranostics. Especially, research focusing on in vivo biodistribution studies of intrinsically radiolabeled UCNPs after intravenous injection is of utmost importance for the potential clinical translation of such formulations. Here, we utilized the gamma emission from 169 Er and 171 Er radionuclides for the demonstration of radiolabeled ZnAl 2 O 4 : 171/169 Er 3+ as a potent agent for dual-modality SPECT/optical imaging. No uptake of radio nanoformulation was detected in the skeleton after 4 h of administration, which evidenced the robust integrity of ZnAl 2 O 4 : 169/171 Er 3+ . Combining the therapeutics using the emission of β - particulates from 169 Er and 171 Er will be promising for the radio-theranostic application of the synthesized ZnAl 2 O 4 : 169/171 Er 3+ nanoformulation. Cell toxicity studies of ZnAl 2 O 4 :1%Er 3+ nanoparticles were examined by an MTT assay in B16F10 mouse melanoma cell lines, which demonstrated good biocompatibility. In addition, we explored the mechanism of UCL modulation via defect engineering by Bi 3+ codoping in the ZnAl 2 O 4 :Er 3+ upconversion nanophosphor. The UCL color tuning was successfully achieved from the red to the green region as a function of Bi 3+ codoping concentrations. Further, we tried to establish a correlation of UCL tuning with the intrinsic oxygen and cation vacancy defects as a function of Bi 3+ codoping concentrations with the help of electron paramagnetic resonance (EPR) and positron annihilation lifetime spectroscopy (PALS) studies. This study contributes to building a bridge between nature of defects and UC luminescence that is crucial for the design of advanced UCNPs for theranostics.
Keyphrases
- endoplasmic reticulum
- high resolution
- estrogen receptor
- energy transfer
- breast cancer cells
- photodynamic therapy
- quantum dots
- oxidative stress
- stem cells
- high dose
- low dose
- ionic liquid
- computed tomography
- high throughput
- cell therapy
- pet ct
- mesenchymal stem cells
- pain management
- single molecule
- pet imaging
- climate change
- chronic pain
- adverse drug
- skin cancer
- case control