Abstract

Tailor-made NIR emitting dyes were designed as multimodal optical probes. These asymmetric amphiphilic compounds show combined intense absorption in the visible region, NIR fluorescence emission, high two-photon absorption in the NIR (with the maximum located around 1000 nm) as well as large Stokes' shift values and second-harmonic generation ability. Thanks to their structure, high loading into nanoemulsions (NEs) could be achieved leading to very high one- and two-photon brightness. These dyes were demonstrated to act as multimodal contrast agents able to generate different optical modalities of interest for bioimaging. Indeed, the uptake and carrier behaviour of the dye-loaded NEs into cancer cells could be monitored by simultaneous two-photon fluorescence and second-harmonic generation optical imaging. Multimodal imaging provided deep insight into the mechanism and kinetics of dye internalisation. Quite interestingly, the nature of the dyes was also found to influence both the kinetics of endocytosis and the internalisation pathways in glioblastoma cancer cells. By modulating the charge distribution within the dyes, the NEs can be tuned to escape lysosomes and enter the mitochondria. Moreover, surface functionalization with PEG macromolecules was realized to yield stealth NIRF-NEs which could be used for in vivo NIRF imaging of subcutaneous tumours in mice.

Highlights

  • Non-invasive molecular imaging has great potential for human clinical use both for diagnosis and treatment

  • Thanks to the presence of the two alkyl chains on the terminal nitrogen and of the positively charged opposite acceptor end-group, the hemicyanine dyes show amphiphilic features which were meant to bestow them high affinity for the lipid corona of NEs

  • Due to their non-centrosymmetric structure and amphiphilic features, these dyes were aimed to orientate in the lipid corona of NEs or the outer lea et of lipidic membranes and generate second harmonic generation (SHG)

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Summary

Introduction

Non-invasive molecular imaging has great potential for human clinical use both for diagnosis and treatment. The brightest ones raise concerns in terms of safety as both acute and chronic toxicity have been demonstrated.[5] In contrast, NIRF dyes may show improved biocompatibility as is the case for indocyanine green and methylene blue which are approved uorescent tracers. Still, these dyes present several restrictions including limited brightness in water, concentration-dependent aggregation and non-speci c binding to plasma proteins.[6]

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