Cyclodextrin Encapsulated pH Sensitive Dyes as Fluorescent Cellular Probes: Self-Aggregation and In Vitro Assessments.
Monica-Cornelia SardaruOana CarpElena-Laura UrsuAnda-Mihaela CraciunCorneliu CojocaruMihaela SilionVladyslava KovalskaIonel I MangalagiuRamona DanacAlexandru RotaruPublished in: Molecules (Basel, Switzerland) (2020)
We have designed and synthesized a series of novel, supramolecular, long-lived fluorescent probes based on the host-guest inclusion complexes formation between fluorescent indolizinyl-pyridinium salts and β-cyclodextrin. Fluorescence and electrospray ionisation mass spectrometry experiments, supported by theoretical molecular docking studies, were utilized in the monitoring of the inclusion complexes formation, evidencing the appearance of corresponding 1:1 and 1:2 species. Additionally, the influence of the guest molecule over the aggregation processes of the cyclodextrin inclusion complexes was investigated by transmission electron microscopy. The absence of cytotoxicity, cellular permeability, long-lived intracellular fluorescence, and in time specific accumulation within acidic organelles identified the investigated supramolecular entities as remarkable candidates for intracellular fluorescence probes. Co-staining experiments using specific organelle markers revealed the fact that, after a 24-h incubation period, the inclusion complexes accumulate predominantly in lysosomes rather than in mitochondria. This study opens new possibilities for a broad range of fluorescent dyes with solubility and high toxicity issues, able to form inclusion complexes with β-cyclodextrin, to be tested as intracellular fluorescence probes.
Keyphrases
- living cells
- single molecule
- energy transfer
- mass spectrometry
- quantum dots
- atomic force microscopy
- capillary electrophoresis
- fluorescent probe
- ionic liquid
- molecular docking
- small molecule
- reactive oxygen species
- fluorescence imaging
- liquid chromatography
- water soluble
- oxidative stress
- label free
- photodynamic therapy
- nucleic acid
- single cell
- endothelial cells
- simultaneous determination