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Multi-luminescent hybrid gadolinium oxide nanoparticles as potential cell labeling
J Fizet1, C Rivière, J L Bridot
1Université de Lyon, Lyon F-69003, France.
Journal of Nanoscience and Nanotechnology
|November 14, 2009
Summary
Newly developed hybrid gadolinium oxide nanoparticles offer efficient and stable cell labeling. These magnetic and optical tracers show excellent photostability and are safely internalized by cells for in-vitro and in-vivo applications.
Area of Science:
- Nanotechnology
- Biomedical Engineering
- Materials Science
Background:
- Developing advanced cell-labeling tracers is crucial for biological research.
- Existing tracers often face limitations in stability, photostability, or biocompatibility.
Purpose of the Study:
- To analyze the utility of novel hybrid gadolinium oxide nanoparticles as multi-labeling cell tracers.
- To evaluate their efficiency, stability, and biocompatibility for in-vitro cell tracking.
Main Methods:
- Synthesis of core-shell gadolinium oxide nanoparticles with embedded organic dyes (FITC, RBITC) and poly(ethylene glycol) functionalization.
- In-vitro cell uptake studies in human fibroblasts and MCF7 cells using optical imaging.
- Confocal microscopy for intracellular distribution analysis and ICP-MS for gadolinium quantification.
- Assessment of cell growth and photostability of encapsulated dyes.
Main Results:
- Efficient and rapid internalization of nanoparticles into both cell lines without causing cell alteration.
- Fluorescent labeling detected within 10 minutes, concentrated in the perinuclear region, and detectable for over 3 days.
- Polysiloxane shell significantly enhances the photostability of rhodamine B isothiocyanate (RBITC), comparable to Alexa 595.
Conclusions:
- Hybrid gadolinium oxide nanoparticles are effective, stable, and biocompatible multi-labeling tracers for cell tracking.
- The polysiloxane shell provides crucial protection, enhancing dye photostability and overall nanoparticle performance.
- These nanoparticles present a versatile solution for assessing cell fate in both in-vitro and in-vivo settings.

