Optical and X-ray Fluorescent Nanoparticles for Dual Mode Bioimaging.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33587608.
- Also identified by DOI 10.1021/acsnano.0c10127 and PMC identifier 8028327.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Nanoparticle (NP) based contrast agents detectable via different imaging modalities (multimodal properties) provide a promising strategy for noninvasive diagnostics. Core-shell NPs combining optical and X-ray fluorescence properties as bioimaging contrast agents are presented. NPs developed earlier for X-ray fluorescence computed tomography (XFCT), based on ceramic molybdenum oxide (MoO<sub>2</sub>) and metallic rhodium (Rh) and ruthenium (Ru), are coated with a silica (SiO<sub>2</sub>) shell, using ethanolamine as the catalyst. The SiO<sub>2</sub> coating method introduced here is demonstrated to be applicable to both metallic and ceramic NPs. Furthermore, a fluorophore (Cy5.5 dye) was conjugated to the SiO<sub>2</sub> layer, without altering the morphological and size characteristics of the hybrid NPs, rendering them with optical fluorescence properties. The improved biocompatibility of the SiO<sub>2</sub> coated NPs without and with Cy5.5 is demonstrated <i>in vitro</i> by Real-Time Cell Analysis (RTCA) on a macrophage cell line (RAW 264.7). The multimodal characteristics of the core-shell NPs are confirmed with confocal microscopy, allowing the intracellular localization of these NPs <i>in vitro</i> to be tracked and studied. <i>In situ</i> XFCT successfully showed the possibility of <i>in vivo</i> multiplexed bioimaging for multitargeting studies with minimum radiation dose. Combined optical and X-ray fluorescence properties empower these NPs as effective macroscopic and microscopic imaging tools.
Medical subject headings
- Nanoparticles
- Silicon Dioxide