Synthesis, Characterization, Spectroscopic, and Electrochemiluminescence Properties of a Solvatochromic Azacrown-Containing Cyanoruthenate(II): Potential Applications in Separation and Indirect Photometric Detection of Cations and Amino Acids in HPLC

2006 ◽  
Vol 12 (13) ◽  
pp. 3528-3537 ◽  
Author(s):  
Mei-Jin Li ◽  
Ben Wai-Kin Chu ◽  
Vivian Wing-Wah Yam
Author(s):  
Jorge Aguilera ◽  
Víctor García-González ◽  
Manuel Alatorre-Meda ◽  
Eustolia Rodríguez-Velázquez ◽  
Ignacio Rivero

In this work, we explored the synthesis of 4,4-difluoro-4-bora-3a,4a-diazas-indacene (BODIPYs) bound to five different amino acids (BODIPY-FAA) (glycine, alanine, leucine, phenylalanine, and tyrosine) (amino group is kept protected with fluorophore Fmoc) and evaluated these conjugates in terms of (i) their photophysical properties and (ii) their potential application as cell staining agents of suspension and adherent cells at healthy and stress conditions. In general, all synthesized BODIPY-FAA (3a-3e) were found to emit fluorescence in the blue and green regions of the spectrum (depending on the solvent conditions). However, BODIPY-FTyr(trt) (3e) showed the best molar extinction coefficient (ε = 28,198 M-1 cm-1) and quantum yield (Φ = 0.17). Biologically speaking, all synthesized conjugates demonstrated a selective affinity for the cytoplasm of Langerhans β-cells employed as a model, being the BODIPY-FLeu conjugate the one displaying the highest observed intensity. As such, our results reveal the BODIPY-FAA as a novel attractive tool for the specific staining of the cell cytoplasm, demonstrating not only a dual fluorescence emission but also a sensing capability to recognize different cell states.


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