Abstract

Biological thiols are antioxidants essential for the prevention of disease. For example, low levels of the tripeptide glutathione are associated with heart disease, cancer, and dementia. Mn2+-doped wide bandgap semiconductor nanocrystals exhibit luminescence and magnetic properties that make them attractive for bimodal imaging. We found that these nanocrystals and silica-encapsulated nanoparticle derivatives exhibit enhanced luminescence in the presence of thiols in both organic solvent and aqueous solution. The key to using these nanocrystals as sensors is control over their surfaces. The addition of a ZnS barrier layer or shell produces more stable nanocrystals that are isolated from their surroundings, and luminescence enhancement is only observed with thinner, intermediate shells. Tunability is demonstrated with dodecanethiol and sensitivities decrease with thin, medium, and thick shells. Turn-on nanoprobe luminescence is also generated by several biological thiols, including glutathione, N-acetylcysteine, cysteine, and dithiothreitol. Nanoparticles prepared with different ZnS shell thicknesses demonstrated varying sensitivity to glutathione, which allows for the tuning of particle sensitivity without optimization. The small photoluminescence response to control amino acids and salts indicates selectivity for thiols. Preliminary magnetic measurements highlight the challenge of optimizing sensors for different imaging modalities. In this work, we assess the prospects of using these nanoparticles as luminescent turn-on thiol sensors and for MRI.

Highlights

  • Imaging of biological environments is a critical strategy for the discovery and treatment of disease [1,2,3]

  • This paper investigates water-soluble Mn2+:ZnSe/ZnS@SiO2 nanoparticles (NPs) with tunable, turn-on luminescence in the presence of biological thiols

  • This behavior was first observed in organic solvent, and can be preserved in aqueous solution when a silica shell is added to the NCs

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Summary

Introduction

Imaging of biological environments is a critical strategy for the discovery and treatment of disease [1,2,3]. The desire to resolve microscopic events spatially and temporally has led to a multitude of imaging probes, which provide advances in resolution, sensitivity, targeting, and treatment [4,5,6,7]. Despite these advances, no single probe possesses all the properties necessary for comprehensive diagnostics. No single probe possesses all the properties necessary for comprehensive diagnostics This limitation sparked an interest in combining imaging modalities to take advantage of their complementary abilities [8,9]. Development of new and improved multimodal probes is an active area of interdisciplinary research, and advances make earlier identification and real-time monitoring of various diseases possible

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