Persistent Luminescence Nanosensors: A Generalized Optode-based Platform for Autofluorescence-free Sensing in Biological Systems

07 February 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Fluorescent nanosensors have drastically progressed our ability to accelerate diagnostics and quantify cellular dynamics in real time. Their modular assembly allows for facile sensor tuning, leading to a large expansion of analytes and systems that can be analyzed. Still, separating sensor signals from background optical signatures remains a major hurdle in the field. Exploiting this modular synthesis, we merged optode-based sensing with near-infrared emitting ZnGa2O4:Cr3+ persistent luminescence nanoparticles (PLNPs) to create functional nanocompo- sites for autofluorescence-free “glow-in-the-dark” sensing. We hydrophobically modified the PLNP surface with covalently bound ligands and incorporated the PLNPs into the polymeric core of optode-based nanoparticles. We demonstrate persistent luminescence nanosensors (PLNs) for five different analytes (K+, Na+, Ca2+, pH, and O2) based on two different sensing mechanisms. The PLNs allowed us to achieve autofluorescence-free quantification of K+ in fetal bovine serum and ratiometric metabolic monitoring of microbial samples with time-resolved luminescence acquisition. We foresee that this approach will allow for high signal-to-noise ratios while sensing in optically challenging samples.

Keywords

Persistent Luminescence
Phosphor
Nanosensor
Optode
Glow-in-the-dark
Nanocomposite
Chemosensor
Oxygen Sensor

Supplementary materials

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Supplementary Information
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The included Supporting Information provides all materials and methods for the manuscript as well as the excitation spectrum and further luminescence lifetime characterization of the as-synthesized ZnGa2O4:Cr3+, the nanocomposite size and zeta potential with different loaded components and block copolymers, additional calibrations that demonstrate functional lifetime, reversibility, selectivity, and sensor mechanism, and all optical channels for the high throughput metabolic assay that was not included in the main text.
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